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1. Fluorescence based studies on the interaction and characterization of surface-active ionic liquids with polarity sensitive intramolecular charge transfer probe

Author: Dhiman Ray, Dipak Chamlagai, Sugam Kumar, Vinod K. Aswal, and Sivaprasad Mitra
Subjects: intramolecular charge transfer, surface active ionic liquids, fluorescence, TCSPC, critical micelle concentration, Physics, QC1-999, Chemistry, QD1-999
Abstract: Surface-active ionic liquids (SAILs) are of tremendous interest in recent times due to their improved application in the field of food, detergent, and health. The modulated fluorescence behavior of an intramolecular charge transfer (ICT) probe, trans‐ethyl‐p‐(dimethylamino) cinnamate (EDAC), in presence of five different SAILs with varying head groups (viz. imidazolium, pyridinium, and morpholinium) and different alkyl chain length (decyl, dodecyl, and tetradecyl) was monitored by steady state and time-resolved fluorescence spectroscopy. Extreme sensitivity of EDAC fluorescence was used to characterize different physicochemical properties of the SAILs, including critical micelle concentration, static polarity, and empirical solvent polarity scale, ET(30) of the microenvironment. The estimated parameters are in good agreement with the literature reports and measured independently from other complimentary experiments discussed here. Time‐resolved fluorescence experiments show a significant retardation in different nonradiative decay channels of EDAC, when compared to that in aqueous phase, indicating a preferential association of the probe in presence of SAILs. The results indicate that the physicochemical properties of SAILs can be tuned by controlling the nature of both the cations and as well as the chain length of the alkyl group. These properties also show significant modulation in solutions with varying SAIL concentration, particularly in the pre- and post-micellar region. The results, particularly the surface-active properties and the self-assembly behavior presented in this study, are expected to provide new knowledge towards the design and development of novel SAILs with specific industrial and biological applications.
Published: 2023
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2. Therapeutic potency of substituted chromones as Alzheimer’s drug: Elucidation of acetylcholinesterase inhibitory activity through spectroscopic and molecular modelling investigation

Author: Prayasee Baruah, Mostofa Ataur Rohman, Semen O. Yesylevskyy, and Sivaprasad Mitra
Subjects: acetylcholinesterase inhibition, ad drug, chromones, pas binding, stacking interactions, thioflavin t fluorescence, Medicine (General), R5-920, Biology (General), QH301-705.5
Abstract: Introduction: Documentation on the potency of chromones as acetylcholinesterase (AChE) antagonists has paved the way for the design and usage of new chromone analogues as inhibitors of AChE modelled on the hypothesis based on cholinergic pathway of Alzheimer’s disease (AD). Here, 2 minimally substituted chromones, namely 3-cyanochromone (CyC) and 7-amino-3-methylchromone (AMC), were checked for their AChE inhibition efficacies and plasma protein modulation. Methods: Colorimetric enzymatic assay as well as fluorescence measurements were performed for obtaining the experimental results, which were further corroborated by molecular docking and simulation studies. Results: The investigated systems exhibited strong inhibition activities against AChE, with CyC (IC50= 85.12 ± 6.70 nM) acting as better inhibitor than AMC (IC50 = 103.09 ± 11.90 nM) and both having IC50 values in the range of FDA approved cholinergic drug Donepezil (IC50 = 74.13 ± 8.30 nM). Non-competitive inhibition was observed in both the cases with the inhibitors binding near the peripheral anionic site (PAS) of the enzyme. Having one planar nitrile group in CyC as compared to sp3 hybridised substituents in AMC facilitated stacking interactions in the former, accounting for its higher inhibitory efficacy. A significant decrease in the inhibition potency of CyC (~32%) was noted in comparison with AMC (~5%) when the experiments were performed in presence of human serum albumin (HSA) instead of pure aqueous buffer. Conclusion: This comparative study affirms the importance of meticulous substitution in the chromone scaffold to promote maximum inhibition potency, while considering their usage as AD drugs.
Published: 2019
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3. Molecular Insights on the Modulated Acetylcholinesterase Inhibition Activity of Tacrine Adsorbed on Biocompatible Graphene Oxide

Author: Pynskhemborlang T. Phanrang, Imocha Rajkumar Singh, Jahnabi Upadhyaya, Asit K. Chandra, and Sivaprasad Mitra
Subjects: General Chemistry
Published: 2023
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4. Modulated Antimicrobial Activity and Drug-Protein Interaction Ability of Zinc Oxide and Cadmium Sulfide Nanoparticles: Effect of Doping with Few First-Row Transition Metals

Author: Imocha Rajkumar Singh, Upashna Chettri, Piyali Maity, Anup K. Ghosh, S. R. Joshi, and Sivaprasad Mitra
Subjects: General Materials Science, General Chemistry, Condensed Matter Physics, Biochemistry
Published: 2022
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5. Therapeutic opportunities of surface-active ionic liquids: a case study on acetylcholinesterase, citrate synthase and HeLa cell lines

Author: Prayasee Baruah, Dhiman Ray, Ibemhanbi Konthoujam, Abhinandan Das, Suman Chakrabarty, Kripamoy Aguan, and Sivaprasad Mitra
Subjects: Materials Chemistry, General Chemistry, Catalysis
Abstract: In concurrence with the pursuit of clean and green medium, recent years have witnessed an unprecedented rise in the usage of ionic liquids (ILs).
Published: 2022
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6. Iodine(<scp>iii</scp>)-promoted regioselective and efficient synthesis of β-triazolyl BODIPYs for the selective recognition of nickel ions and bovine serum albumin

Author: Bintu Kumar, Anindita Bhatta, Prakriti Saraf, Krishnan Rangan, Madhushree Sarkar, Sivaprasad Mitra, and Dalip Kumar
Subjects: Boron Compounds, Ions, Inorganic Chemistry, Azides, Nickel, Serum Albumin, Bovine, Iodides, Iodine
Abstract: Novel β-triazolyl BODIPYs were synthesized by iodine(iii)-promoted direct C–H functionalization for the sensitive and selective detection of Ni2+ ions and BSA protein.
Published: 2022
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7. Deciphering Spectroscopic and Structural Insights into the Photophysical Behavior of 2,2′-Dipyridylamine: An Efficient Environment Sensitive Fluorescence Probe

Author: Dipak Chamlagai, Sivaprasad Mitra, Pynskhemborlang T. Phanrang, and Mostofa Ataur Rohman
Subjects: Solvent, Chemistry, Hydrogen bond, Excited state, Solvatochromism, Density functional theory, Steady state (chemistry), Physical and Theoretical Chemistry, Ground state, Photochemistry, Fluorescence
Abstract: Excited state deactivation properties and the effects of solvent hydrogen bonding (HB) on the photophysical behavior of 2,2'-dypyridylamine (DPyA) were investigated by steady state and time-resolved fluorescence experiments, molecular docking, and density functional theory (DFT) calculations. In addition to the polarity effect, the contributions of solvent HB donation (HBD) acidity and HB acceptance (HBA) basicity to modulate the solvatochromic spectral properties were estimated from multiparametric linear regression analysis using Kamlet-Taft (KT) and Catalan formalisms. The importance of C-N bond torsion, leading to the trans → cis conversion, was manifested by substantial increase in DPyA fluorescence yield in the presence of cyclodextrin (CD) and glycerol. The unusually low fluorescence yield in aqueous medium was explained on the basis of synergistic effect of solvent hydrogen bonding combined with excited state conformational isomerization, which renders DPyA to be an excellent environment sensitive fluorescence reporter. The experimental results were verified with structural insights obtained from DFT calculations at B3LYP/6-311++G(d,p) level and construction of potential energy surface (PES) in the ground state as well as in the excited states.
Published: 2021
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8. Sulfonylurea Class of Antidiabetic Drugs Inhibit Acetylcholinesterase Activity: Unexplored Auxiliary Pharmacological Benefit toward Alzheimer’s Disease

Author: Sivaprasad Mitra, Abhinandan Das, Suman Chakrabarty, Prayasee Baruah, Debojit Paul, and Kripamoy Aguan
Subjects: Pharmacology, Drug, Chlorpropamide, Chemistry, medicine.drug_class, media_common.quotation_subject, Acetylcholinesterase, Sulfonylurea, chemistry.chemical_compound, Tolbutamide, Non-competitive inhibition, embryonic structures, medicine, Pharmacology (medical), Donepezil, IC50, medicine.drug, media_common
Abstract: [Image: see text] Contemporary literature documents extensive research on common causative mechanisms, pathogenic pathways and dual effective remedies for Alzheimer’s disease (AD) and Type 2 diabetes mellitus (T2DM). Tolbutamide (TBM), chlorpropamide (CPM), and glyburide (GLY) are three sulfonylurea antidiabetic drugs of different generations. All these drugs were found to exhibit moderate to strong inhibitory efficiency on the neurotransmitter degrading enzyme acetylcholinesterase (AChE) with GLY (IC(50) = 0.74 ± 0.02 μM) being the most potent, followed by CPM (IC(50) = 5.72 ± 0.24 μM) and TBM (IC(50) = 28.9 ± 1.60 μM). Notably, the inhibition efficiency of GLY is even comparable with the FDA approved AD drug, donepezil (DON). The larger size of GLY spans almost the full gorge of AChE ranging from catalytic active site (CAS) to the peripheral active site (PAS) with relatively strong binding affinity (6.0 × 10(5) M(–1)) and acts as a competitive inhibitor for AChE. On the other hand, while they show relatively weak binding ((2–6) × 10(4) M(–1)), both CPM and TBM act as noncompetitive binders. While these two drugs can bind to PAS, MD simulation results predict an alternative noncompetitive inhibition mechanism for CPM. These results open the possibility of repurposing the antidiabetic drugs, particularly GLY, in the treatment of AD. The consequential side effect of excess acetylcholine production, due to the administration of these drugs to AD-unaffected patients, can be rectified by using colloidal gold and silver nanofluids as potential AChE activity boosters.
Published: 2021
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9. Visible light-promoted synthesis of pyrrolidinone derivatives via Rose Bengal as a photoredox catalyst and their photophysical studies

Author: Rishanlang Nongkhlaw, Arup Dutta, Ridaphun Nongrum, Mostofa Ataur Rohman, Aiborlang Thongni, and Sivaprasad Mitra
Subjects: Chemistry, Intramolecular force, Materials Chemistry, Photoredox catalysis, General Chemistry, Steady state (chemistry), Photochemistry, Fluorescence, Radical cyclization, Catalysis, Fluorescence spectroscopy, Visible spectrum
Abstract: Herein, we report an intramolecular radical cyclization reaction towards the synthesis of pyrrolidinone derivatives via metal-free photoredox catalysis under irradiation from blue LEDs. Some of the remarkable features of this protocol include synthetic efficiency, green reaction profile, easy isolation of products and short reaction time. The photophysical properties of synthesized compounds were investigated via steady state and time-resolved fluorescence spectroscopy in the solid state. Results showed the promising opportunity for their spectral tuning together with large Stokes-shifted and highly active fluorescence emission, thus indicating that these molecular scaffolds can be effective probes for the biological applications and development of opto-electronic devices.
Published: 2021
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10. Cholinergic drugs bind at the minor groove and reverse induced oxidative stress of calf thymus DNA: a new perspective towards an unexplored therapeutic efficacy

Author: Prayasee Baruah, Kripamoy Aguan, Sivaprasad Mitra, Pynskhemborlang T. Phanrang, and Ibemhanbi Konthoujam
Subjects: 0303 health sciences, Chemistry, Perspective (graphical), General Chemistry, 010402 general chemistry, medicine.disease_cause, 01 natural sciences, Catalysis, 0104 chemical sciences, Cell biology, 03 medical and health sciences, Materials Chemistry, medicine, Cholinergic, Oxidative stress, 030304 developmental biology, Minor groove
Abstract: Four FDA approved cholinesterase inhibitors reverse the hydrogen peroxide induced oxidative damage of ct-DNA.
Published: 2021
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11. Auxiliary Therapeutic Role of Cholinergic Agents: Mechanistic Insights into the Antioxidant Behavior of Alzheimer's Disease Drugs

Author: Pynskhemborlang T. Phanrang, Prayasee Baruah, Asit K. Chandra, and Sivaprasad Mitra
Subjects: Molecular Docking Simulation, Pharmaceutical Preparations, Alzheimer Disease, Cholinergic Agents, Humans, Physical and Theoretical Chemistry, Antioxidants
Abstract: Repurposing of existing drugs toward new therapeutic use(s) has become an emergent area of research in current times. In this context, the antioxidant behavior of eight cholinergic drugs used in the treatment of Alzheimer's disease (AD) was investigated theoretically. The low bond dissociation enthalpy values in all of the compounds advocated for the hydrogen atom transfer mechanism toward the observed antioxidant behavior. The kinetic study for the reaction of the drugs with hydroperoxyl radicals indicated an indirect reaction path owing to the presence of pre- and postreaction complexes. In some cases, the rate constant for the H-abstraction reaction (
Published: 2022

12. Combined experimental and computational studies on the photophysical properties of systematically substituted polypyridyl based ligands on a benzene core

Author: Dipak Chamlagai, Pynskhemborlang T. Phanrang, Lincoln Dkhar, K. Mohan Rao, and Sivaprasad Mitra
Subjects: General Chemical Engineering, General Physics and Astronomy, General Chemistry
Published: 2023
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13. Elevated Fibrinogen Level Reduces Therapeutic Efficiency of AD Drugs: Biophysical Insights into the Interaction of FDA-Approved Cholinesterase Inhibitors with Human Fibrinogen

Author: Prayasee Baruah, Debojit Paul, Jitesh Doshi, and Sivaprasad Mitra
Subjects: Pharmaceutical Preparations, Alzheimer Disease, Materials Chemistry, Acetylcholinesterase, Tacrine, Fibrinogen, Humans, Cholinesterase Inhibitors, Physical and Theoretical Chemistry, Surfaces, Coatings and Films
Abstract: Despite being the second most abundant protein in blood plasma, reports on the interaction of drugs with fibrinogen (FIB) are relatively scarce. The effect of FIB on the therapeutic potency of four FDA-approved Alzheimer's disease drugs, namely, tacrine (TAC), donepezil (DON), eserine (ESE), and huperzine (HUP), was investigated through a combination of different in vitro and in silico experiments. The efficiency of the drugs in inhibiting the activity of acetylcholinesterase (AChE) was significantly reduced in the presence of FIB. This effect was even found to be more substantial than that for the most abundant plasma protein, human serum albumin (HSA). For example, the relative change in IC
Published: 2021

14. Modulation of drug binding ability and augmented enzymatic activity of lysozyme stabilized in presence of surface-active ionic liquids

Author: Dhiman Ray, Imocha Rajkumar Singh, Anindita Bhatta, Abhinandan Das, Suman Chakrabarty, and Sivaprasad Mitra
Subjects: Materials Chemistry, Physical and Theoretical Chemistry, Condensed Matter Physics, Spectroscopy, Atomic and Molecular Physics, and Optics, Electronic, Optical and Magnetic Materials
Published: 2022
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15. Modulated photophysical properties and sequestration of potent anti-acetylcholinesterase active coumarinyl dyes in human serum albumin

Author: Anindita Bhatta, Prayasee Baruah, Pynskhemborlang T. Phanrang, Grace Basumatary, Ghanashyam Bez, and Sivaprasad Mitra
Subjects: Process Chemistry and Technology, General Chemical Engineering
Published: 2022
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16. Excited State Decay Dynamics in 3‐Formyl‐4‐hydroxy Benzoic Acid: Understanding the Global Picture of an ESIPT‐Driven Multiple‐Emissive Species

Author: Prakriti Ranjan Bangal, Mostofa Ataur Rohman, Dipankar Sutradhar, Asit K. Chandra, and Sivaprasad Mitra
Subjects: chemistry.chemical_compound, Materials science, chemistry, Excited state, Dynamics (mechanics), General Chemistry, Time-resolved spectroscopy, Photochemistry, Benzoic acid
Published: 2019
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17. Specific solvent effect on the photophysical behavior of substituted chromones: A combined fluorescence, DFT and MD study

Author: Prayasee Baruah, Semen O. Yesylevskyy, Mostofa Ataur Rohman, and Sivaprasad Mitra
Subjects: 010304 chemical physics, Hydrogen bond, Solvatochromism, General Physics and Astronomy, 010402 general chemistry, 01 natural sciences, Fluorescence spectroscopy, 0104 chemical sciences, Solvent, chemistry.chemical_compound, Molecular dynamics, chemistry, Computational chemistry, 0103 physical sciences, Chromone, Density functional theory, Physical and Theoretical Chemistry, Solvent effects
Abstract: Solvent dependent photophysical properties of two chromone derivatives, namely 7-amino-2-methyl chromone (AMC) and 3-cyano chromone (CyC), were studied by time-resolved fluorescence spectroscopy, density functional theory (DFT) calculation and molecular dynamics (MD) simulation. Contributions from different solvatochromic parameters were quantitatively estimated using Lippert-Mataga relation, uni-parametric ET(30) and multi-parametric Kamlet–Taft and/or Catalan relations. Notable solvatochromic shift in emission peak was estimated for CyC (Δλ = 130 nm) in comparison with AMC (Δλ = 53 nm). While both solvent hydrogen bond donation acidity and acceptance basicity is important in AMC photophysics, the latter is insignificant for CyC. Estimation of hydrogen bonding pattern in hydrated structures of AMC and CyC derived from MD simulation reveals that specific hydrogen bond donation of the solvent to carbonyl oxygen of the chromones is the most important microstructure modulating the spectral behavior in both the cases, augmenting the experimental observation as well as DFT results.
Published: 2019
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18. Fluorescence solvatochromism and modulated anticholinergic activity of novel coumarin compounds sequestered in human serum albumin nanocavities

Author: Mostofa Ataur Rohman, Prayasee Baruah, Deboshika Bhattacharjee, B. Myrboh, and Sivaprasad Mitra
Subjects: Circular dichroism, Coumarin Compound, medicine.drug_class, Solvatochromism, 02 engineering and technology, General Chemistry, 010402 general chemistry, 021001 nanoscience & nanotechnology, Human serum albumin, Coumarin, 01 natural sciences, Fluorescence, Catalysis, 0104 chemical sciences, Solvent, chemistry.chemical_compound, chemistry, Materials Chemistry, medicine, Biophysics, Anticholinergic, 0210 nano-technology, medicine.drug
Abstract: A coumarin compound, 3,3′-methylenebis(4-hydroxy-2H-chromen-2-one) (MHC), and its substituted derivative, 3,3′-(phenylmethylene)bis(4-hydroxy-2H-chromen-2-one) (MHCB), possess potent anticholinergic activities, which were found to be reduced significantly in the presence of human serum albumin (HSA). The molecular interactions responsible for sequestering MHC and MHCB were explored by steady-state and time-resolved fluorescence using the modulated solvatochromic behavior of the probes as a fluorescent marker. A quantitative description of the different solvent parameters responsible for the notable solvent-dependent photo-physical properties of the investigated systems was extracted from multiple linear regression analysis of the experimental data using the Kamlet–Taft and Catalan formalisms. A series of complimentary studies involving circular dichroism measurement and molecular docking calculations revealed that the binding of both coumarin derivatives resulted in the stabilization of the α-helical structure of human serum albumin (HSA). However, significant differences in binding mechanism were noted in terms of the strength, mode and principal forces responsible for the spontaneous association of the probes into the protein-binding domain.
Published: 2019
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19. Interaction of chlorpropamide with serum albumin: Effect on advanced glycated end (AGE) product fluorescence

Author: Sivaprasad Mitra and Imocha Rajkumar Singh
Subjects: Glycation End Products, Advanced, Chlorpropamide, Arabinose, Glycosylation, Serum albumin, 02 engineering and technology, 010402 general chemistry, 01 natural sciences, Analytical Chemistry, Hydrophobic effect, chemistry.chemical_compound, Glycation, medicine, Humans, Hypoglycemic Agents, Instrumentation, Serum Albumin, Spectroscopy, Drug Carriers, biology, Fructose, 021001 nanoscience & nanotechnology, Human serum albumin, Atomic and Molecular Physics, and Optics, 0104 chemical sciences, Molecular Docking Simulation, Spectrometry, Fluorescence, Biochemistry, chemistry, Galactose, embryonic structures, biology.protein, 0210 nano-technology, human activities, medicine.drug
Abstract: Carrier proteins like bovine or human serum albumin (BSA and HSA, respectively) are prone to glycation as compared to the other available proteins. In this study, reducing sugars such as l-arabinose (ara), d-(-) galactose (gal) and d-(-) fructose (fru) were used to create model glycated serum albumins and binding ability of these with well-known antidiabetic drug chlorpropamide (CPM) was monitored. Fluorescence quenching experiment revealed that interaction of CPM with native as well as glycated albumins undergoes through a ground state complex formation. CPM binds strongly to glycated HSA with arabinose (gHSAara) as compared to other glycated systems and to the native proteins. CPM interacts through Van der Waals and hydrogen bonding interaction to glycated BSA by d-(-) fructose (gBSAfru) and also with native HSA; whereas, it's interaction with BSA and others glycated systems like gBSAara, gBSAgal and gHSAara occurs primarily through hydrophobic interaction. CPM showed an enhancement in the production of the advanced glycated end products (AGE) in all the glycated proteins. The difference in the binding capability of CPM to differently glycated albumins could be a major model to understand the drug carrying capacity of the glycated serum albumins.
Published: 2019
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20. Dietary polyphenols inhibit plasma protein arabinosylation: Biomolecular interaction of genistein and ellagic acid with serum albumins

Author: Semen O. Yesylevskyy, Imocha Rajkumar Singh, and Sivaprasad Mitra
Subjects: Quenching (fluorescence), biology, Organic Chemistry, Biophysics, Genistein, Polyphenols, Biochemistry, Fluorescence, Blood proteins, chemistry.chemical_compound, chemistry, Polyphenol, Docking (molecular), biology.protein, Humans, Bovine serum albumin, Serum Albumin, Ellagic acid
Abstract: The mode of interaction of polyphenolic compounds like genistein (GTN) and ellagic acid (EGA) with human and bovine serum albumin (HSA and BSA, respectively) was found to differ significantly. Stern-Volmer (SV) analysis of the fluorescence quenching data revealed that the binding strength of EGA (1.9 ± 0.09 × 105 M−1) to HSA is about one order of magnitude higher than GTN (2.24 ± 0.06 × 104 M−1). While the static quenching of HSA fluorescence was found to proceed through simple Stern-Volmer (SV) mechanism, a quenching sphere-of-action model was indispensable for BSA. Temperature dependent fluorescence along with a series of other biophysical experiments and ensemble docking calculation revealed that EGA and GTN bind to the serum proteins primarily through the entropy driven process. The α-helical content and the microenvironment near Trp residue of HSA and BSA did not show any appreciable change due to the binding of either GTN or EGA. Interestingly, both GTN and EGA were found to inhibit the formation of advanced glycated end (AGE) product of serum proteins up to the extent of 70–90% within 12–24 h. Relatively moderate binding propensity along with the anti-glycation ability of the polyphenols confirmed that GTN and EGA can be used either as an alternative or towards development of suitable drugs in the prevention of many diabetic-related complications.
Published: 2021

21. Photophysical behavior of systematically substituted (di-2-pyridylaminomethyl) benzene ligands and its Re(I) complexes: A combined experimental and theoretical approach

Author: Dipankar Sutradhar, K. Mohan Rao, Mostofa Ataur Rohman, Sivaprasad Mitra, S. Sangilipandi, and Asit K. Chandra
Subjects: 010405 organic chemistry, Chemistry, Hydrogen bond, Ligand, General Chemical Engineering, General Physics and Astronomy, General Chemistry, 010402 general chemistry, Photochemistry, 01 natural sciences, Fluorescence spectroscopy, 0104 chemical sciences, Solvent, Crystallography, Density functional theory, Molecular orbital, Time-resolved spectroscopy, Natural bond orbital
Abstract: The photophysical behavior of a series of flexible di-2-pyridylaminomethyl substituted ligands systematically substituted on a rigid benzene core and their corresponding mono-metallic Re(I) complexes have been investigated by steady state and time-resolved fluorescence spectroscopy in different composition of DMSO–water binary solvent mixtures. Unusual fluorescence properties in lower DMSO content ( X DMSO = 0.1–0.3) solvent mixtures is consistent with fascinating property of DMSO, which is known to perturb the hydrogen bonding ability of water with the solute. Spin allowed inter-ligand π–π * transition is more apparent in (1, 3) substituted systems. The calculated spectroscopic parameters of the complexes are significantly different from the ligands, mainly due to ligand to metal charge transfer. The experimental observations are in very good agreement with the theoretical results obtained at B3LYP/6-31G(d,p)/LANL2DZ level of density functional theory (DFT) calculation. Natural bond orbital (NBO) analysis and examination of frontier molecular orbitals reveal that the basic architecture of the symmetrically substituted multi-chromophoric ligand can induce excitation energy hopping, similar to an artificial antenna system.
Published: 2017
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22. Homoleptic Ti[ONO]2type complexes of amino‐acid‐tethered phenolato Schiff‐base ligands: Synthesis, characterization, time‐resolved fluorescence spectroscopy, and cytotoxicity against ovarian and colon cancer cells

Author: Sivaprasad Mitra, Edit Y. Tshuva, Rajesh Manne, Edward R. T. Tiekink, Mostofa Ataur Rohman, Zohar Shpilt, and Tushar S. Basu Baul
Subjects: chemistry.chemical_classification, Steric effects, Schiff base, 010405 organic chemistry, General Chemistry, 010402 general chemistry, 01 natural sciences, Medicinal chemistry, 0104 chemical sciences, Amino acid, Inorganic Chemistry, chemistry.chemical_compound, Hydrolysis, Molecular geometry, chemistry, Reactivity (chemistry), Solubility, Homoleptic
Abstract: Six homoleptic Ti(IV) compounds of dianionic tridentate Schiff base ligands were synthesized from chiral amino acids, 2-hydroxybenzaldehyde and Ti(OiPr)4. The compounds were spectroscopically characterized and the molecular geometries were established by X-ray crystallography. The ligands coordinated the titanium via carboxylate-O-, imine-N-, and phenoxide-O atoms. Two isomers were identified; each based on a trans-N2O4 donor set, but one with trans carboxylate-O atoms and another with each carboxylate-O atom trans to a phenoxide-O atom. Photophysical profiles exhibited faster excited-state relaxation in the solid phase than in solution. Marked cytotoxicities were recorded toward human ovarian A2780 and colon HT-29 cancer cells with IC50 values ranging between 23±2 and 103±3 µM. Comparative hydrolytic stability studies by NMR in 10% D2O solutions provided t1/2 values of up to 15±2 h, with little correlation to cytotoxicity implying a role of hydrolysis products in the reactivity and identifying steric bulk as a contributor to stability and solubility.
Published: 2019
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23. Modulated Protein Binding Ability of Anti-Diabetic Drugs in Presence of Monodispersed Gold Nanoparticles and its Inhibitory Potential towards Advanced Glycated End (AGE) Product Formation

Author: Sivaprasad Mitra and Imocha Rajkumar Singh
Subjects: Glycation End Products, Advanced, Chlorpropamide, Sociology and Political Science, Surface Properties, Tolbutamide, Clinical Biochemistry, Serum albumin, Metal Nanoparticles, 010402 general chemistry, 01 natural sciences, Biochemistry, Hydrophobic effect, Animals, Hypoglycemic Agents, Colloids, Bovine serum albumin, Particle Size, Protein secondary structure, Spectroscopy, Binding Sites, biology, 010405 organic chemistry, Chemistry, Temperature, Serum Albumin, Bovine, Fluorescence, 0104 chemical sciences, Clinical Psychology, Spectrometry, Fluorescence, Colloidal gold, Drug delivery, Biophysics, biology.protein, Cattle, Adsorption, Gold, Law, Hydrophobic and Hydrophilic Interactions, Social Sciences (miscellaneous), Conjugate
Abstract: Binding strength of the anti-diabetic drugs chlorpropamide (CPM) and tolbutamide (TBM) with model protein bovine serum albumin (BSA) shows strong modulation in presence of colloidal gold nanoparticles (AuNP). Intrinsic tryptophan fluorescence of both the native BSA and BSA-AuNP conjugate quenched in presence of the drugs. Stern-Volmer quenching constant (KSV) of CPM binding to BSA-AuNP conjugate at different temperatures is almost twice (6.76~14.76 × 103 M−1) than the corresponding values in native BSA (3.21~5.72 × 103 M−1). However, the calculated KSV values with TBM show certain degree of reduction in presence of AuNP (6.46× 103 M−1), while comparing with native BSA (8.83 × 103 M−1). The binding mode of CPM towards BSA-AuNP conjugate is mainly through hydrophobic forces; whereas, TBM binding is identified to be Van der Waal’s and hydrogen bonding type of interaction. Fluorescence lifetime analysis confirms static type of quenching for the intrinsic tryptophan fluorescence of BSA as well as BSA-AuNP conjugate with addition of CPM and TBM at different concentrations. The α-helical content in the secondary structure of BSA is decreased to 48.32% and 45. 28% in presence of AuNP, when the concentration of CPM is 0.08 mM and 0.16 mM in comparison with that of native protein (50.13%). On the other hand, the intensity of sugar induced advanced glycated end (AGE) product fluorescence is decreased by 55% and 80% at 0.13 nM and 0.68 nM AuNP, respectively. Change in the binding strength of the drugs with transport protein and reduced AGE product formation in presence of AuNP could lead to a major development in the field of nanomedicine and associated drug delivery techniques.
Published: 2019

24. Search for dark matter produced in association with a single top quark or a top quark pair in proton-proton collisions at √s=13 TeV

Author: Tobias Pook, Jay Hauser, A. Vilela Pereira, O. Gonzalez Lopez, Michael Brodski, David J. Smith, Olivér Surányi, S. M. A. Ghiasi Shirazi, C. Barth, Olena Karacheban, Andrius Juodagalvis, Elizabeth Sexton-Kennedy, Matthias Wolf, Tariq Aziz, Dave M Newbold, A. Khan, Gouranga Kole, Bruno Galinhas, Paolo Ronchese, Badder Marzocchi, Sanjay Kumar Swain, Marc M Baarmand, Andrea Gozzelino, A. Starodumov, K. Hurtado Anampa, Jian Wang, Ravi Janjam, Siddharth Narayanan, Marko Dragicevic, Daniele Trocino, Anton Karneyeu, Leonard Apanasevich, Kerstin Borras, Giacomo Fedi, M. Vander Donckt, Jochen Schieck, Virgil E Barnes, Miagkov Miagkov, George Karathanasis, Shalhout Shalhout, Y. Choi, Guido Tonelli, Dong-Chul Son, Liliana Teodorescu, R. Wilkinson, Charalambos Nicolaou, Brandon Allen, Dustin Burns, C. Mills, Winston Ko, I. De Bruyn, Reza Goldouzian, Mohd Nizam Yusli, Y. Chen, Niki Saoulidou, Sercan Sen, Ngoc-Khanh Tran, Aaron Bundock, Katerina Lipka, Martin Kirakosyan, S. Fonseca De Souza, D. P. Stickland, Zhenyu Chen, Simone Pigazzini, Stefano Colafranceschi, C. Scharf, Siarhei Shulha, L. J. Sanchez Rosas, Urs Langenegger, M. Schroeder, Geoffrey Smith, Alessio Ghezzi, Renato Potenza, S. Slabospitskii, E. Eskut, James Keaveney, Zeljko Antunovic, Martino Dall'Osso, Asif Saddique, Christoph Paus, Piergiulio Lenzi, Weinan Si, Robert M Harris, Rostyslav Shevchenko, Hallie Trauger, G. Correia Silva, Elliot Hughes, C. Neu, Adrian Byszuk, Thong Nguyen, Johannes Haller, Andreas Hinzmann, Guenter Eckerlin, F. Vazquez Valencia, Clément Leloup, Christian Schomakers, Alexander Nikitenko, Paolo Gunnellini, Marcin Konecki, V Rusinov, Constantin Heidegger, Batool Safarzadeh, Juliet Ritchie Patterson, Joao Varela, Aruna Nayak, Michael Plagge, Gervasio Gomez, Armen Tumasyan, Paula Eerola, Metin Yalvac, Stephan Lammel, Manoj Sharan, L. K. Saini, Hugo Delannoy, Daniel Noonan, Alessandro Rossi, Mia Tosi, L. 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R.M., Hasegawa S., Hirschauer J., Hu Z., Jayatilaka B., Jindariani S., Johnson M., Joshi U., Klima B., Kortelainen M.J., Kreis B., Lammel S., Lincoln D., Lipton R., Liu M., Liu T., Lykken J., Maeshima K., Marraffino J.M., Mason D., McBride P., Merkel P., Mrenna S., Nahn S., O'Dell V., Pedro K., Pena C., Prokofyev O., Rakness G., Ristori L., Savoy-Navarro A., Schneider B., Sexton-Kennedy E., Soha A., Spalding W.J., Spiegel L., Stoynev S., Strait J., Strobbe N., Taylor L., Tkaczyk S., Tran N.V., Uplegger L., Vaandering E.W., Vernieri C., Verzocchi M., Vidal R., Wang M., Weber H.A., Whitbeck A., Acosta D., Avery P., Bortignon P., Bourilkov D., Brinkerhoff A., Cadamuro L., Carnes A., Curry D., Field R.D., Gleyzer S.V., Joshi B.M., Konigsberg J., Korytov A., Lo K.H., Ma P., Matchev K., Mitselmakher G., Rosenzweig D., Shi K., Sperka D., Wang J., Zuo X., Joshi Y.R., Linn S., Ackert A., Adams T., Askew A., Hagopian S., Hagopian V., Johnson K.F., Kolberg T., Martinez G., Perry T., Prosper H., Saha A., Schiber C., Yohay R., Baarmand M.M., Bhopatkar V., Colafranceschi S., Hohlmann M., Noonan D., Rahmani M., Roy T., Yumiceva F., Adams M.R., Apanasevich L., Berry D., Betts R.R., Cavanaugh R., Chen X., Dittmer S., Evdokimov O., Gerber C.E., Hangal D.A., Hofman D.J., Jung K., Kamin J., Mills C., Tonjes M.B., Varelas N., Wang H., Wang X., Wu Z., Zhang J., Alhusseini M., Bilki B., Clarida W., Dilsiz K., Durgut S., Gandrajula R.P., Haytmyradov M., Khristenko V., Merlo J.-P., Mestvirishvili A., Moeller A., Nachtman J., Ogul H., Onel Y., Ozok F., Penzo A., Snyder C., Tiras E., Wetzel J., Blumenfeld B., Cocoros A., Eminizer N., Fehling D., Feng L., Gritsan A.V., Hung W.T., Maksimovic P., Roskes J., Sarica U., Swartz M., Xiao M., You C., Al-bataineh A., Baringer P., Bean A., Boren S., Bowen J., Bylinkin A., Castle J., Khalil S., Kropivnitskaya A., Majumder D., Mcbrayer W., Murray M., Rogan C., Sanders S., Schmitz E., Tapia Takaki J.D., Duric S., Ivanov A., Kaadze K., Kim D., Maravin Y., Mendis D.R., Mitchell T., Modak A., Mohammadi A., Rebassoo F., Wright D., Baden A., Baron O., Belloni A., Eno S.C., Feng Y., Ferraioli C., Hadley N.J., Jabeen S., Jeng G.Y., Kellogg R.G., Kunkle J., Mignerey A.C., Nabili S., Ricci-Tam F., Seidel M., Shin Y.H., Skuja A., Tonwar S.C., Wong K., Abercrombie D., Allen B., Azzolini V., Baty A., Bauer G., Bi R., Brandt S., Busza W., Cali I.A., D'Alfonso M., Demiragli Z., Gomez Ceballos G., Goncharov M., Harris P., Hsu D., Hu M., Iiyama Y., Innocenti G.M., Klute M., Kovalskyi D., Lee Y.-J., Luckey P.D., Maier B., Marini A.C., Mcginn C., Mironov C., Narayanan S., Niu X., Paus C., Roland C., Roland G., Shi Z., Stephans G.S.F., Sumorok K., Tatar K., Velicanu D., Wang T.W., Wyslouch B., Benvenuti A.C., Chatterjee R.M., Evans A., Hansen P., Hiltbrand J., Kalafut S., Krohn M., Kubota Y., Lesko Z., Mans J., Ruckstuhl N., Rusack R., Wadud M.A., Acosta J.G., Oliveros S., Avdeeva E., Bloom K., Claes D.R., Fangmeier C., Golf F., Gonzalez Suarez R., Kamalieddin R., Kravchenko I., Monroy J., Siado J.E., Snow G.R., Stieger B., Godshalk A., Harrington C., Iashvili I., Kharchilava A., Mclean C., Nguyen D., Parker A., Rappoccio S., Roozbahani B., Alverson G., Barberis E., Freer C., Haddad Y., Hortiangtham A., Morse D.M., Orimoto T., Wamorkar T., Wang B., Wisecarver A., Wood D., Bueghly J., Charaf O., Gunter T., Hahn K.A., Odell N., Schmitt M.H., Sung K., Trovato M., Velasco M., Bucci R., Dev N., Hildreth M., Hurtado Anampa K., Jessop C., Karmgard D.J., Lannon K., Li W., Loukas N., Marinelli N., Meng F., Mueller C., Musienko Y., Planer M., Reinsvold A., Ruchti R., Siddireddy P., Smith G., Taroni S., Wayne M., Wightman A., Wolf M., Woodard A., Alimena J., Antonelli L., Bylsma B., Durkin L.S., Flowers S., Francis B., Hill C., Ji W., Ling T.Y., Luo W., Winer B.L., Cooperstein S., Elmer P., Hardenbrook J., Haubrich N., Higginbotham S., Kalogeropoulos A., Kwan S., Lange D., Lucchini M.T., Luo J., Marlow D., Mei K., Ojalvo I., Olsen J., Palmer C., Piroue P., Salfeld-Nebgen J., Stickland D., Tully C., Norberg S., Barker A., Barnes V.E., Das S., Gutay L., Jones M., Jung A.W., Khatiwada A., Mahakud B., Miller D.H., Neumeister N., Peng C.C., Piperov S., Qiu H., Schulte J.F., Sun J., Wang F., Xiao R., Xie W., Cheng T., Dolen J., Parashar N., Chen Z., Ecklund K.M., Freed S., Geurts F.J.M., Kilpatrick M., Padley B.P., Redjimi R., Roberts J., Rorie J., Shi W., Tu Z., Zhang A., Bodek A., de Barbaro P., Demina R., Duh Y., Dulemba J.L., Fallon C., Ferbel T., Galanti M., Garcia-Bellido A., Han J., Hindrichs O., Khukhunaishvili A., Ranken E., Tan P., Taus R., Chou J.P., Gershtein Y., Halkiadakis E., Hart A., Heindl M., Hughes E., Kaplan S., Kunnawalkam Elayavalli R., Kyriacou S., Laflotte I., Lath A., Montalvo R., Nash K., Osherson M., Saka H., Salur S., Schnetzer S., Sheffield D., Somalwar S., Stone R., Thomas S., Thomassen P., Delannoy A.G., Heideman J., Riley G., Spanier S., Bouhali O., Celik A., Dalchenko M., De Mattia M., Delgado A., Dildick S., Eusebi R., Gilmore J., Huang T., Kamon T., Luo S., Marley D., Mueller R., Overton D., Pernie L., Rathjens D., Safonov A., Akchurin N., Damgov J., De Guio F., Dudero P.R., Kunori S., Lamichhane K., Mengke T., Muthumuni S., Peltola T., Undleeb S., Volobouev I., Greene S., Gurrola A., Janjam R., Johns W., Maguire C., Melo A., Ni H., Padeken K., Romeo F., Ruiz Alvarez J.D., Sheldon P., Tuo S., Velkovska J., Verweij M., Xu Q., Arenton M.W., Barria P., Cox B., Hirosky R., Joyce M., Ledovskoy A., Li H., Neu C., Sinthuprasith T., Wolfe E., Xia F., Harr R., Karchin P.E., Poudyal N., Sturdy J., Thapa P., Zaleski S., Buchanan J., Caillol C., Carlsmith D., Dasu S., De Bruyn I., Dodd L., Gomber B., Grothe M., Herndon M., Herve A., Hussain U., Klabbers P., Lanaro A., Long K., Loveless R., Ruggles T., Savin A., Smith N., Smith W.H., Woods N., CMS Collaboration, Özdemir, Kadri, Çukurova Üniversitesi, Fen-Edebiyat Fakültesi, Fizik Bölümü, Institut de Recherches sur les lois Fondamentales de l'Univers (IRFU), Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Université Paris-Saclay, Laboratoire Leprince-Ringuet (LLR), Centre National de la Recherche Scientifique (CNRS)-École polytechnique (X)-Institut National de Physique Nucléaire et de Physique des Particules du CNRS (IN2P3), Institut Pluridisciplinaire Hubert Curien (IPHC), Institut National de Physique Nucléaire et de Physique des Particules du CNRS (IN2P3)-Université de Strasbourg (UNISTRA)-Centre National de la Recherche Scientifique (CNRS), Université de Haute-Alsace (UHA) Mulhouse - Colmar (Université de Haute-Alsace (UHA)), Centre de Calcul de l'IN2P3 (CC-IN2P3), Institut National de Physique Nucléaire et de Physique des Particules du CNRS (IN2P3)-Centre National de la Recherche Scientifique (CNRS), Institut de Physique Nucléaire de Lyon (IPNL), Centre National de la Recherche Scientifique (CNRS)-Université Claude Bernard Lyon 1 (UCBL), Université de Lyon-Université de Lyon-Institut National de Physique Nucléaire et de Physique des Particules du CNRS (IN2P3), CMS, Sirunyan, A, Tumasyan, A, Adam, W, Ambrogi, F, Asilar, E, Bergauer, T, Brandstetter, J, Dragicevic, M, Erö, J, Escalante Del Valle, A, Flechl, M, Frühwirth, R, Ghete, V, Hrubec, J, Jeitler, M, Krammer, N, Krätschmer, I, Liko, D, Madlener, T, Mikulec, I, Rad, N, Rohringer, H, Schieck, J, Schöfbeck, R, Spanring, M, Spitzbart, D, Waltenberger, W, Wittmann, J, Wulz, C, Zarucki, M, Chekhovsky, V, Mossolov, V, Suarez Gonzalez, J, De Wolf, E, Di Croce, D, Janssen, X, Lauwers, J, Pieters, M, Van Haevermaet, H, Van Mechelen, P, Van Remortel, N, Abu Zeid, S, Blekman, F, D’Hondt, J, De Clercq, J, Deroover, K, Flouris, G, Lontkovskyi, D, Lowette, S, Marchesini, I, Moortgat, S, Moreels, L, Python, Q, Skovpen, K, Tavernier, S, Van Doninck, W, Van Mulders, P, Van Parijs, I, Beghin, D, Bilin, B, Brun, H, Clerbaux, B, De Lentdecker, G, Delannoy, H, Dorney, B, Fasanella, G, Favart, L, Goldouzian, R, Grebenyuk, A, Kalsi, A, Lenzi, T, Luetic, J, Postiau, N, Starling, E, Thomas, L, Vander Velde, C, Vanlaer, P, Vannerom, D, Wang, Q, Cornelis, T, Dobur, D, Fagot, A, Gul, M, Khvastunov, I, Poyraz, D, Roskas, C, Trocino, D, Tytgat, M, Verbeke, W, Vermassen, B, Vit, M, Zaganidis, N, Bakhshiansohi, H, Bondu, O, Brochet, S, Bruno, G, Caputo, C, David, P, Delaere, C, Delcourt, M, Giammanco, A, Krintiras, G, Lemaitre, V, Magitteri, A, Piotrzkowski, K, Saggio, A, Vidal Marono, M, Vischia, P, Wertz, S, Zobec, J, Alves, F, Alves, G, Correa Martins Junior, M, Correia Silva, G, Hensel, C, Moraes, A, Pol, M, Rebello Teles, P, Belchior Batista Das Chagas, E, Carvalho, W, Chinellato, J, Coelho, E, Da Costa, E, Da Silveira, G, De Jesus Damiao, D, De Oliveira Martins, C, Fonseca De Souza, S, Malbouisson, H, Matos Figueiredo, D, Melo De Almeida, M, Mora Herrera, C, Mundim, L, Nogima, H, Prado Da Silva, W, Sanchez Rosas, L, Santoro, A, Sznajder, A, Thiel, M, Tonelli Manganote, E, Torres Da Silva De Araujo, F, Vilela Pereira, A, Ahuja, S, Bernardes, C, Calligaris, L, Fernandez Perez Tomei, T, Gregores, E, Mercadante, P, Novaes, S, Padula, S, Aleksandrov, A, Hadjiiska, R, Iaydjiev, P, Marinov, A, Misheva, M, Rodozov, M, Shopova, M, Sultanov, G, Dimitrov, A, Litov, L, Pavlov, B, Petkov, P, Fang, W, Gao, X, Yuan, L, Ahmad, M, Bian, J, Chen, G, Chen, H, Chen, M, Chen, Y, Jiang, C, Leggat, D, Liao, H, Liu, Z, Shaheen, S, Spiezia, A, Tao, J, Wang, Z, Yazgan, E, Zhang, H, Zhang, S, Zhao, J, Ban, Y, Levin, A, Li, J, Li, L, Li, Q, Mao, Y, Qian, S, Wang, D, Wang, Y, Avila, C, Cabrera, A, Carrillo Montoya, C, Chaparro Sierra, L, Florez, C, González Hernández, C, Segura Delgado, M, Courbon, B, Godinovic, N, Lelas, D, Puljak, I, Sculac, T, Antunovic, Z, Kovac, M, Brigljevic, V, Ferencek, D, Kadija, K, Mesic, B, Starodumov, A, Susa, T, Ather, M, Attikis, A, Kolosova, M, Mavromanolakis, G, Mousa, J, Nicolaou, C, Ptochos, F, Razis, P, Rykaczewski, H, Finger, M, Ayala, E, Carrera Jarrin, E, 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Chen, X, Dittmer, S, Evdokimov, O, Gerber, C, Hangal, D, Hofman, D, Jung, K, Kamin, J, Mills, C, Tonjes, M, Varelas, N, Wang, H, Wang, X, Wu, Z, Zhang, J, Alhusseini, M, Bilki, B, Clarida, W, Dilsiz, K, Durgut, S, Gandrajula, R, Haytmyradov, M, Khristenko, V, Merlo, J, Mestvirishvili, A, Moeller, A, Nachtman, J, Ogul, H, Onel, Y, Ozok, F, Penzo, A, Snyder, C, Tiras, E, Wetzel, J, Blumenfeld, B, Cocoros, A, Eminizer, N, Fehling, D, Feng, L, Gritsan, A, Hung, W, Maksimovic, P, Roskes, J, Sarica, U, Swartz, M, Xiao, M, You, C, Al-bataineh, A, Baringer, P, Bean, A, Boren, S, Bowen, J, Bylinkin, A, Castle, J, Khalil, S, Kropivnitskaya, A, Majumder, D, Mcbrayer, W, Murray, M, Rogan, C, Sanders, S, Schmitz, E, Tapia Takaki, J, Duric, S, Ivanov, A, Kaadze, K, Maravin, Y, Mendis, D, Mitchell, T, Modak, A, Mohammadi, A, Rebassoo, F, Wright, D, Baden, A, Baron, O, Belloni, A, Eno, S, Feng, Y, Ferraioli, C, Hadley, N, Jabeen, S, Jeng, G, Kellogg, R, Kunkle, J, Mignerey, A, Nabili, S, Ricci-Tam, F, 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T, Wamorkar, T, Wang, B, Wisecarver, A, Wood, D, Bueghly, J, Charaf, O, Gunter, T, Hahn, K, Odell, N, Schmitt, M, Sung, K, Trovato, M, Velasco, M, Bucci, R, Dev, N, Hildreth, M, Hurtado Anampa, K, Jessop, C, Karmgard, D, Lannon, K, Li, W, Loukas, N, Marinelli, N, Meng, F, Mueller, C, Musienko, Y, Planer, M, Reinsvold, A, Ruchti, R, Siddireddy, P, Smith, G, Taroni, S, Wayne, M, Wightman, A, Wolf, M, Woodard, A, Alimena, J, Antonelli, L, Bylsma, B, Durkin, L, Flowers, S, Francis, B, Hill, C, Ji, W, Ling, T, Luo, W, Winer, B, Cooperstein, S, Elmer, P, Hardenbrook, J, Haubrich, N, Higginbotham, S, Kalogeropoulos, A, Kwan, S, Lange, D, Lucchini, M, Luo, J, Marlow, D, Mei, K, Ojalvo, I, Olsen, J, Palmer, C, Piroué, P, Salfeld-Nebgen, J, Stickland, D, Tully, C, Norberg, S, Barker, A, Barnes, V, Das, S, Gutay, L, Jones, M, Jung, A, Khatiwada, A, Mahakud, B, Miller, D, Neumeister, N, Peng, C, Piperov, S, Qiu, H, Schulte, J, Sun, J, Wang, F, Xiao, R, Xie, W, Cheng, T, Dolen, J, Parashar, N, Chen, Z, Ecklund, K, Freed, S, Geurts, F, Kilpatrick, M, Padley, B, Redjimi, R, Roberts, J, Rorie, J, Shi, W, Tu, Z, Zhang, A, Bodek, A, de Barbaro, P, Demina, R, Duh, Y, Dulemba, J, Fallon, C, Ferbel, T, Galanti, M, Garcia-Bellido, A, Han, J, Hindrichs, O, Khukhunaishvili, A, Ranken, E, Tan, P, Taus, R, Chou, J, Gershtein, Y, Halkiadakis, E, Hart, A, Heindl, M, Hughes, E, Kaplan, S, Kunnawalkam Elayavalli, R, Kyriacou, S, Laflotte, I, Lath, A, Montalvo, R, Nash, K, Osherson, M, Saka, H, Salur, S, Schnetzer, S, Sheffield, D, Somalwar, S, Stone, R, Thomas, S, Thomassen, P, Delannoy, A, Heideman, J, Riley, G, Spanier, S, Bouhali, O, Celik, A, Dalchenko, M, De Mattia, M, Delgado, A, Dildick, S, Eusebi, R, Gilmore, J, Huang, T, Kamon, T, Luo, S, Marley, D, Mueller, R, Overton, D, Perniè, L, Rathjens, D, Safonov, A, Akchurin, N, Damgov, J, De Guio, F, Dudero, P, Kunori, S, Lamichhane, K, Mengke, T, Muthumuni, S, Peltola, T, Undleeb, S, Volobouev, I, Greene, S, Gurrola, A, Janjam, R, Johns, W, Maguire, C, Melo, A, Ni, H, Padeken, K, Romeo, F, Ruiz Alvarez, J, Sheldon, P, Tuo, S, Velkovska, J, Verweij, M, Xu, Q, Arenton, M, Barria, P, Cox, B, Hirosky, R, Joyce, M, Ledovskoy, A, Li, H, Neu, C, Sinthuprasith, T, Wolfe, E, Xia, F, Harr, R, Karchin, P, Poudyal, N, Sturdy, J, Thapa, P, Zaleski, S, Buchanan, J, Caillol, C, Carlsmith, D, Dasu, S, De Bruyn, I, Dodd, L, Gomber, B, Grothe, M, Herndon, M, Hervé, A, Hussain, U, Klabbers, P, Lanaro, A, Long, K, Loveless, R, Ruggles, T, Savin, A, Smith, N, Smith, W, Woods, N, Department of Physics, Helsinki Institute of Physics, Institut National de Physique Nucléaire et de Physique des Particules du CNRS (IN2P3)-École polytechnique (X)-Centre National de la Recherche Scientifique (CNRS), Université de Strasbourg (UNISTRA)-Centre National de la Recherche Scientifique (CNRS), Centre National de la Recherche Scientifique (CNRS)-Institut National de Physique Nucléaire et de Physique des Particules du CNRS (IN2P3), Université Claude Bernard Lyon 1 (UCBL), Université de Lyon-Université de Lyon-Institut National de Physique Nucléaire et de Physique des Particules du CNRS (IN2P3)-Centre National de la Recherche Scientifique (CNRS), Yerevan Phys Inst, Inst Hochenergiephys, Inst Nucl Problems, Univ Antwerp, Vrije Univ Brussel, Univ Libre Bruxelles, Univ Ghent, Catholic Univ Louvain, Ctr Brasileiro Pesquisas Fis, Universidade do Estado do Rio de Janeiro (UERJ), Universidade Estadual Paulista (Unesp), Universidade Federal do ABC (UFABC), Bulgarian Acad Sci, Univ Sofia, Beihang Univ, Inst High Energy Phys, Peking Univ, Tsinghua Univ, Univ Los Andes, Univ Split, Inst Rudjer Boskovic, Univ Cyprus, Charles Univ Prague, Escuela Politec Nacl, Univ San Francisco Quito, Acad Sci Res & Technol Arab Republ Egypt, NICPB, Univ Helsinki, Helsinki Inst Phys, Lappeenranta Univ Technol, Univ Paris Saclay, Univ Strasbourg, CNRS IN2P3, Univ Claude Bernard Lyon 1, Georgian Tech Univ, Tbilisi State Univ, Rhein Westfal TH Aachen, Deutsches Elektronen Synchrotron, Univ Hamburg, Karlsruher Inst Technol, NCSR Demokritos, Univ Athens, Natl Tech Univ Athens, Univ Ioannina, Eotvos Lorand Univ, Wigner Res Ctr Phys, Inst Nucl Res ATOMKI, Univ Debrecen, Indian Inst Sci IISc, HBNI, Panjab Univ, Univ Delhi, Indian Inst Technol Madras, Bhabha Atom Res Ctr, Tata Inst Fundamental Res A, Tata Inst Fundamental Res B, IISER, Inst Res Fundamental Sci IPM, Univ Coll Dublin, INFN Sez Bari, Univ Bari, Politecn Bari, INFN Sez Bologna, Univ Bologna, INFN Sez Catania, Univ Catania, INFN Sez Firenze, Univ Firenze, INFN Lab Nazl Frascati, INFN Sez Genova, INFN Sez Milano Bicocca, Univ Milano Bicocca, INFN Sez Napoli, Univ Napoli Federico II, Univ Basilicata, Univ G Marconi, INFN Sez Padova, Univ Padua, Univ Trento, INFN Sez Pavia, Univ Pavia, INFN Sez Perugia, Univ Perugia, INFN Sez Pisa, Univ Pisa, Scuola Normale Super Pisa, INFN Sez Roma, Sapienza Univ Roma, INFN Sez Torino, Univ Turin, Univ Piemonte Orientale, INFN Sez Trieste, Univ Trieste, Kyungpook Natl Univ, Chonnam Natl Univ, Hanyang Univ, Korea Univ, Sejong Univ, Seoul Natl Univ, Univ Seoul, Sungkyunkwan Univ, Vilnius Univ, Univ Malaya, Univ Sonora UNISON, IPN, Univ Iberoamer, Benemerita Univ Autonoma Puebla, Univ Autonoma San Luis Potosi, Univ Auckland, Univ Canterbury, Quaid I Azam Univ, Natl Ctr Nucl Res, Univ Warsaw, Lab Instrumentacao & Fis Expt Particulas, Joint Inst Nucl Res, Petersburg Nucl Phys Inst, Inst Nucl Res, Inst Theoret & Expt Phys, Moscow Inst Phys & Technol, Natl Res Nucl Univ, PN Lebedev Phys Inst, Lomonosov Moscow State Univ, NSU, Natl Res Ctr, Natl Res Tomsk Polytech Univ, Univ Belgrade, Vinca Inst Nucl Sci, Ctr Invest Energet Medioambientales & Tecnol CIEM, Univ Autonoma Madrid, Univ Oviedo, Univ Cantabria, Univ Ruhuna, CERN, Paul Scherrer Inst, Swiss Fed Inst Technol, Univ Zurich, Natl Cent Univ, NTU, Chulalongkorn Univ, Cukurova Univ, Middle East Tech Univ, Bogazici Univ, Istanbul Tech Univ, Natl Acad Sci Ukraine, Natl Sci Ctr, Univ Bristol, 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Sci, British Univ Egypt, Suez Univ, Zewail City Sci & Technol, King Abdulaziz Univ, Univ Haute Alsace, Brandenburg Tech Univ Cottbus, IIT Bhubaneswar, Inst Phys, Shoolini Univ, Visva Bharati Univ, Isfahan Univ Technol, Islamic Azad Univ, Univ Siena, Scuola Normale, Sezione Ist Nazl Fis Nucl, Kyung Hee Univ, Int Islamic Univ Malaysia, MOSTI, Consejo Nacl Ciencia & Technol, Warsaw Univ Technol, St Petersburg State Polytech Univ, Budker Inst Nucl Phys, Riga Tech Univ, Gaziosmanpasa Univ, Adiyaman Univ, Istanbul Aydin Univ, Mersin Univ, Piri Reis Univ, Ozyegin Univ, Izmir Inst Technol, Marmara Univ, Kafkas Univ, Istanbul Univ, Istanbul Bilgi Univ, Hacettepe Univ, Univ Southampton, Monash Univ, Bethel Univ, Karamanoglu Mehmetbey Univ, Utah Valley Univ, Beykent Univ, Bingol Univ, Sinop Univ, Mimar Sinan Univ, Texas A&M Univ Qatar, Belforte, S., Candelise, V., Casarsa, M., Cossutti, F., DA ROLD, A., DELLA RICCA, G., Vazzoler, F., Zanetti, A., ET AL (the CMS, Collaboration), Karapınar, Güler, Izmir Institute of Technology. Mathematics, CMS Collaboration (ukupan broj autora: 2290), Université de Strasbourg (UNISTRA)-Université de Haute-Alsace (UHA) Mulhouse - Colmar (Université de Haute-Alsace (UHA))-Institut National de Physique Nucléaire et de Physique des Particules du CNRS (IN2P3)-Centre National de la Recherche Scientifique (CNRS), and Sağır, Sinan
Subjects: Top quark, Proton, top: single production, 13000 GeV-cms, High Energy Physics::Lattice, Nuclear Theory, coupling: scalar, mass [dark matter], pair production [top], channel cross section: upper limit, 7. Clean energy, 01 natural sciences, High Energy Physics - Experiment, high energy physics, experimental particle physics, LHC, CMS, physics, beyond two generations, excited top quark, hadron-hadron scattering (experiments), supersymmetry, beyond standard model, lepton production, data acquisition concepts, detector control systems (detector and experiment monitoring and slow-control systems, architecture, hardware, algorithms, databases), modular electronics, optical detector readout concepts, particle physics experiments, data, Higgs, muon, Physics, Particles & Fields, Hadron-Hadron scattering (experiments), Jets, [PHYS.HEXP]Physics [physics]/High Energy Physics - Experiment [hep-ex], scattering [p p], Collisions, Physics, S030DMP, 02 Physical Sciences, upper limit [channel cross section], Settore FIS/01 - Fisica Sperimentale, dark matter, top physics, Nuclear & Particles Physics, Pseudoscalar, Proton–proton collisions, CERN LHC Coll, Top physics, category, lower limit [mass], Physical Sciences, Physique des particules élémentaires, Centre for High Energy Physics, PARTICLE PHYSICS, colliding beams [p p], top: pair production, Particle Physics - Experiment, signature, Quark, p p: scattering, Nuclear and High Energy Physics, Particle physics, mass: lower limit, Scalar (mathematics), Dark matter, 114 Physical sciences, single production [top], Standard Model, dark matter: associated production, 0103 physical sciences, fermion: dark matter, ddc:530, coupling: pseudoscalar, 010306 general physics, 01 Mathematical Sciences, Science & Technology, LARGE HADRON COLLIDER, hep-ex, 010308 nuclear & particles physics, dark matter: mass, High Energy Physics::Phenomenology, mediation [dark matter], Fermion, dark matter [fermion], dark matter: mediation, pseudoscalar [coupling], scalar [coupling], High Energy Physics::Experiment, associated production [dark matter], Physics, LHC, CMS, Dark Matter, p p: colliding beams, experimental results
Abstract: A search for dark matter produced in association with top quarks in proton-proton collisions at a center-of-mass energy of 13 TeV is presented. The data set used corresponds to an integrated luminosity of 35.9 fb −1 recorded with the CMS detector at the LHC. Whereas previous searches for neutral scalar or pseudoscalar mediators considered dark matter production in association with a top quark pair only, this analysis also includes production modes with a single top quark. The results are derived from the combination of multiple selection categories that are defined to target either the single top quark or the top quark pair signature. No significant deviations with respect to the standard model predictions are observed. The results are interpreted in the context of a simplified model in which a scalar or pseudoscalar mediator particle couples to a top quark and subsequently decays into dark matter particles. Scalar and pseudoscalar mediator particles with masses below 290 and 300 GeV, respectively, are excluded at 95% confidence level, assuming a dark matter particle mass of 1 GeV and mediator couplings to fermions and dark matter particles equal to unity.[Figure not available: see fulltext.]., 0, info:eu-repo/semantics/published
Published: 2019
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25. Fluorescence modulation of two substituted chromone derivatives with human serum albumin

Author: Mostofa Ataur Rohman and Sivaprasad Mitra
Published: 2019
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26. PHOTOPHYSICAL BEHAVIOUR OF SYSTEMATICALLY SUBSTITUTED (DI-2- PYRIDYLAMINOMETHYL) BENZENE LIGANDS

Author: Mostofa Ataur Rohman and Sivaprasad Mitra
Published: 2019
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27. Modulation of enzyme activity at nano-bio interface: A case study with acetylcholinesterase and citrate synthase adsorbed on colloidal metal nanoparticles

Author: Prayasee Baruah, Semen O. Yesylevskyy, Kripamoy Aguan, and Sivaprasad Mitra
Subjects: Intrinsic activity, 02 engineering and technology, 010402 general chemistry, 01 natural sciences, Silver nanoparticle, chemistry.chemical_compound, Materials Chemistry, Citrate synthase, Physical and Theoretical Chemistry, Spectroscopy, chemistry.chemical_classification, biology, Substrate (chemistry), 021001 nanoscience & nanotechnology, Condensed Matter Physics, Acetylcholinesterase, Atomic and Molecular Physics, and Optics, Enzyme assay, 0104 chemical sciences, Electronic, Optical and Magnetic Materials, Enzyme, chemistry, Colloidal gold, Biophysics, biology.protein, 0210 nano-technology
Abstract: The effects of colloidal gold and silver nanoparticles (Au and Ag NP, respectively) were studied on the activity of acetylcholinesterase (AChE), the key enzyme in the pathology of Alzheimer's Disease (AD) and citrate synthase (CS), the mitochondrial enzyme responsible for oxidative metabolism. Being established as a primary basis of neurodegeneration, mitochondrial dysfunction connects both these two enzymes with AD. The in-vitro enzymatic activities are modulated strongly in presence of NPs. The maximum AChE catalytic rate (Vmax) increases by 30% in presence of NP systems. The Michalis-Menten constant (Km) remains unaltered in presence of AuNP; while, ~61.23% increase is noted in presence of AgNP. For the two-substrate enzyme CS, NPs were found to affect only the pathway involving oxaloacetate (OAA) as substrate. In this case, Vmax and Km increased by 21.80% and 46.60%, respectively for AuNP; while the corresponding increase were 18.20% and 33.33%, respectively for AgNP. The binding of AChE on AgNP surface occurred through random contact within very short time scale, followed by slower interaction and contact optimization within tens of nanoseconds. A series of cationic surfactants exhibited optimistic results in restoring the intrinsic activity for both the enzymes. The results highlight neurotoxicity of metal NPs in certain cases like AD and emphasize their use in pharmacological milieu only with suitable accompanying delivery medium like surfactants.
Published: 2021
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28. Screening Indigenous Medicinal Plants of Northeast India for Their Anti-Alzheimer’s Properties

Author: Amarta Kumar Pal, Atanu Bhattacharjee, Sivaprasad Mitra, Kripamoy Aguan, and Roohollah Sobhani
Subjects: 0301 basic medicine, Pharmacology, 03 medical and health sciences, 030109 nutrition & dietetics, 0302 clinical medicine, Anti alzheimer, Traditional medicine, Drug Discovery, Biology, Medicinal plants, 030217 neurology & neurosurgery, Indigenous
Published: 2016
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29. Cholinergic inhibitors replace thioflavin-T from acetylcholinesterase binding pocket: A potential fluorescence based molecular switch

Author: Sivaprasad Mitra and Mullah Muhaiminul Islam
Subjects: Molecular switch, Quenching (fluorescence), Stereochemistry, General Physics and Astronomy, 02 engineering and technology, 010402 general chemistry, 021001 nanoscience & nanotechnology, 01 natural sciences, Fluorescence, Acetylcholinesterase, 0104 chemical sciences, chemistry.chemical_compound, chemistry, Cholinergic, Thioflavin, Steady state (chemistry), Physical and Theoretical Chemistry, 0210 nano-technology, Fluorescence anisotropy
Abstract: The fluorescence intensity of acetylcholinesterase (AChE) bound thioflavin-T (ThT) is found to decrease regularly in presence of cholinergic inhibitors. The quenching phenomenon is not consistent with typical Stern-Volmer mechanism and can be explained on the basis of dynamic replacement of the probe from AChE gorge into the bulk aqueous medium. The resulting modulation in steady state intensity and/or time-dependent fluorescence depolarization forms the basis of a molecular switch between ThT and inhibitors, which can be correlated with AChE inhibition activity of the drugs.
Published: 2016
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30. Lysozyme binding ability toward psychoactive stimulant drugs: Modulatory effect of colloidal metal nanoparticles

Author: Vikash K. Sonu, Mostofa Ataur Rohman, Sivaprasad Mitra, and Mullah Muhaiminul Islam
Subjects: Silver, Stereochemistry, Vasodilator Agents, Metal Nanoparticles, 02 engineering and technology, 010402 general chemistry, 01 natural sciences, Fluorescence, Silver nanoparticle, chemistry.chemical_compound, Colloid and Surface Chemistry, Theophylline, medicine, Animals, Colloids, Physical and Theoretical Chemistry, Theobromine, Binding Sites, Quenching (fluorescence), Hydrogen bond, Hydrogen Bonding, Surfaces and Interfaces, General Medicine, 021001 nanoscience & nanotechnology, 0104 chemical sciences, Molecular Docking Simulation, Spectrometry, Fluorescence, chemistry, Biophysics, Muramidase, Titration, Gold, Lysozyme, 0210 nano-technology, Chickens, Hydrophobic and Hydrophilic Interactions, Protein Binding, Biotechnology, medicine.drug
Abstract: The interaction and binding behavior of the well-known psychoactive stimulant drugs theophylline (THP) and theobromine (THB) with lysozyme (LYS) was monitored by in-vitro fluorescence titration and molecular docking calculations under physiological condition. The quenching of protein fluorescence on addition of the drugs is due to the formation of protein-drug complex in the ground state in both the cases. However, the binding interaction is almost three orders of magnitude stronger in THP, which involves mostly hydrogen bonding interaction in comparison with THB where hydrophobic binding plays the predominant role. The mechanism of fluorescence quenching (static type) remains same also in presence of gold and silver nanoparticles (NPs); however, the binding capacity of LYS with the drugs changes drastically in comparison with that in aqueous buffer medium. While the binding affinity of LYS to THB increases ca. 100 times in presence of both the NPs, it is seen to decrease drastically (by almost 1000 fold) for THP. This significant modulation in binding behavior indicates that the drug transportation capacity of LYS can be controlled significantly with the formation protein-NP noncovalent assembly system as an efficient delivery channel.
Published: 2016
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31. Regioselective synthesis of functionalized [1,6]-naphthyridines by KF/basic alumina as a recyclable catalyst and a brief study of their photophysical properties

Author: Snehadrinarayan Khatua, Mithu Saha, Sivaprasad Mitra, Amarta Kumar Pal, Mullah Muhaiminul Islam, and Sibaji Nandi
Subjects: chemistry.chemical_classification, 010405 organic chemistry, Aryl, Organic Chemistry, Regioselectivity, 010402 general chemistry, Heterogeneous catalysis, 01 natural sciences, 0104 chemical sciences, Catalysis, chemistry.chemical_compound, chemistry, Michael reaction, Organic chemistry, Knoevenagel condensation, Alkyl, Malononitrile
Abstract: An efficient, one-pot, solvent-free, regioselective synthesis of functionalized [1,6]-naphthyridines was explored by a heterogeneous catalyst via a three-component multicomponent reaction (MCR). KF/basic alumina–catalyzed double heteroannulation of aryl alkyl ketones, malononitrile, and alkyl amines generates the compounds with high appendage diversity combinatorially via Knoevenagel condensation followed by Michael addition and cyclization pathway. Short reaction time, high yield, simple reaction technique, and recoverability and reusability of the catalyst without compromising the yield and purity of the compounds are the salient features of this methodology. Additionally, these compounds exhibit promising photophysical properties.
Published: 2016
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32. Modulation of ESIPT fluorescence in o-hydroxy acetophenone derivatives: A comparative study in different bio-mimicking aqueous interfaces

Author: Pynsakhiat Miki Gashnga, T. Sanjoy Singh, and Sivaprasad Mitra
Subjects: chemistry.chemical_classification, Aqueous solution, Cyclodextrin, 02 engineering and technology, 010402 general chemistry, 021001 nanoscience & nanotechnology, Condensed Matter Physics, Photochemistry, 01 natural sciences, Enol, Atomic and Molecular Physics, and Optics, 0104 chemical sciences, Electronic, Optical and Magnetic Materials, Solvent, chemistry.chemical_compound, chemistry, Excited state, Materials Chemistry, Density functional theory, Physical and Theoretical Chemistry, 0210 nano-technology, Conformational isomerism, Spectroscopy, Acetophenone
Abstract: Excited state intramolecular proton transfer (ESIPT) reaction and photophysical behavior of two intramolecularly hydrogen bonded o-hydroxy acetophenone derivatives, namely 2-acetyl-4-methyl-6-nitrophenol (I) and 2-acetyl-4-chloro-6-nitrophenol (II) are studied in the presence of different micro-heterogeneous environments ranging from cyclodextrin, surfactant as well as in model water soluble proteins like bovine and human serum albumin. The appearance of different emission profiles corresponding to a series of excited state isomers like primary enol structure (E), proton transferred keto form (K), or intermolecularly hydrogen bonded (with the solvent) open conformer is rationalized on the basis of varying degree of sequestration and the environment around the probe in the local micro-structure of the hydrophobic domain. The experimental observations are in complete agreement with the fluorescence behavior of these probes in homogeneous solvent medium as well as results based on density functional theory calculation published earlier (Chem. Phys. 342, 2007, 309).
Published: 2016
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33. Human serum albumin reduces the potency of acetylcholinesterase inhibitor based drugs for Alzheimer's disease

Author: Arun Bahadur Gurung, Atanu Bhattacharjee, Sivaprasad Mitra, Mullah Muhaiminul Islam, and Kripamoy Aguan
Subjects: 0301 basic medicine, medicine.drug_class, Serum albumin, Tacrine Hydrochloride, Pharmacology, Toxicology, 03 medical and health sciences, chemistry.chemical_compound, 0302 clinical medicine, Alzheimer Disease, Donepezil Hydrochloride, medicine, Humans, IC50, Serum Albumin, Huperzine A, biology, General Medicine, Human serum albumin, Acetylcholinesterase, Molecular Docking Simulation, Kinetics, 030104 developmental biology, Acetylcholinesterase inhibitor, chemistry, biology.protein, Cholinesterase Inhibitors, 030217 neurology & neurosurgery, medicine.drug
Abstract: Human serum albumin (HSA) induced modulation of acetylcholinesterase (AChE) inhibition activity of four well-known cholinergic inhibitors like tacrine hydrochloride (TAC), donepezil hydrochloride monohydrate (DON), (-) Huperzine A (HuPA), eserine (ESE) was monitored quantitatively by Ellman's method. Kinetic analysis of enzyme hydrolysis reaction revealed that while the mechanism of inhibition does not change significantly, the inhibition efficiency changes drastically in presence of HSA, particularly for DON and TAC. However, interestingly, no notable difference was observed in the cases of HuPA and/or ESE. For example, the IC50 value of AChE inhibition increases by almost 135% in presence of ∼250 μM HSA (IC50 = 159 ± 8 nM) while comparing with aqueous buffer solution of pH 8.0 (IC50 = 68 ± 4 nM) in DON. On the other hand, the change is almost insignificant (
Published: 2016
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34. Caffeine and sulfadiazine interact differently with human serum albumin: A combined fluorescence and molecular docking study

Author: Pynsakhiat Miki Gashnga, Vikash K. Sonu, Sivaprasad Mitra, N. Shaemningwar Moyon, and Mullah Muhaiminul Islam
Subjects: Stereochemistry, Static Electricity, Sulfadiazine, 02 engineering and technology, 010402 general chemistry, 01 natural sciences, Fluorescence, Analytical Chemistry, Hydrophobic effect, chemistry.chemical_compound, Protein structure, Anti-Infective Agents, Caffeine, medicine, Humans, Instrumentation, Serum Albumin, Spectroscopy, Binding Sites, Quenching (fluorescence), 021001 nanoscience & nanotechnology, Human serum albumin, Atomic and Molecular Physics, and Optics, 0104 chemical sciences, Molecular Docking Simulation, chemistry, Lipophilicity, Thermodynamics, Central Nervous System Stimulants, Titration, 0210 nano-technology, Hydrophobic and Hydrophilic Interactions, Protein Binding, medicine.drug
Abstract: The interaction and binding behavior of the well-known drug sulfadiazine (SDZ) and psychoactive stimulant caffeine (CAF) with human serum albumin (HSA) was monitored by in vitro fluorescence titration and molecular docking calculations under physiological condition. The quenching of protein fluorescence on addition of CAF is due to the formation of protein–drug complex in the ground state; whereas in case of SDZ, the experimental results were explained on the basis of sphere of action model. Although both these compounds bind preferentially in Sudlow’s site 1 of the protein, the association constant is approximately two fold higher in case of SDZ (∼4.0 × 10 4 M −1 ) in comparison with CAF (∼9.3 × 10 2 M −1 ) and correlates well with physico-chemical properties like p K a and lipophilicity of the drugs. Temperature dependent fluorescence study reveals that both SDZ and CAF bind spontaneously with HSA. However, the binding of SDZ with the protein is mainly governed by the hydrophobic forces in contrast with that of CAF; where, the interaction is best explained in terms of electrostatic mechanism. Molecular docking calculation predicts the binding of these drugs in different location of sub-domain IIA in the protein structure.
Published: 2016
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35. Search for dijet resonances using events with three jets in proton-proton collisions at s=13TeV

Author: Alexandre Zabi, S. M. A. Ghiasi Shirazi, Tao Huang, Isa Dumanoglu, Marius Teroerde, Davide Zuolo, Georgia Karapostoli, C. Barth, Pieter David, Olga Evdokimov, Andrius Juodagalvis, Stephane Perries, H. El Mamouni, Junghwan Goh, Livio Fanò, Jongjeong Kim, Kerstin Borras, Giacomo Fedi, D. A. Sanz Becerra, Gobinda Majumder, Elisabetta Gallo, Vincenzo Ciriolo, Dong-Chul Son, Liliana Teodorescu, Devanjali Dutta, Jennifer Chu, J. H. Kim, P. Busson, Viktor Khristenko, Aaron Bundock, Katerina Lipka, Martin Kirakosyan, Gaël Perrin, Umesh Joshi, Costas Foudas, Devdatta Majumder, Yasser Assran, Valerie Scheurer, Marius Preuten, Nils Faltermann, Sabino Meola, Roberto Covarelli, Sergio Cittolin, Jared Sturdy, Kaya Tatar, A. Bornheim, Sandra S. Padula, Yiwen Wen, Paolo Vitulo, Andris Skuja, Ivica Puljak, Hans Reithler, M. A. Bhat, C. S. Moon, Georgios Bakas, Robin Aggleton, Ferhat Ozok, C. A. Salazar González, Dominique Gigi, Duong Nguyen, Vladyslav Danilov, F. Vazquez Valencia, Clément Leloup, Andreas Nürnberg, William J Spalding, Jay Roberts, Stefano Bianco, Brandon Chiarito, Doris Eckstein, Achim Geiser, Batoul Diab, Yury Ivanov, Andre Sznajder, Serdal Damarseckin, Ben Bylsma, Alexander Nikitenko, Raffaello D'Alessandro, Nabin Poudyal, Sharon Hagopian, Ralf Ulrich, Jasvinder A. Singh, Prasanna Siddireddy, Alexander Morton, T. Geralis, Mateusz Zarucki, Javier Cuevas, Antoni Shtipliyski, Andrei Sobol, Juliette Alimena, A. P. Singh, Yuri Gershtein, Emmanuelle Perez, Roberto Tenchini, Meng Xiao, Brian L Winer, Mehmet Özgür Sahin, Donato Creanza, Marc Dobson, Heiner Tholen, M. Rahmani, Meena Meena, H. Rejeb Sfar, Jane Nachtman, Sergio F Novaes, Samet Lezki, Marcello Abbrescia, H. Bakhshiansohi, Gabriella Pasztor, Paul Asmuss, E. J. Tonelli Manganote, G. G. Da Silveira, Cristina Riccardi, Francois Lagarde, Jacobo Konigsberg, Umberto Dosselli, M. Gola, Ekaterina Kuznetsova, Vincenzo Innocente, Sanjay Kumar, Danila Tlisov, Alexei Safonov, Morgan Lethuillier, Yasar Onel, Erich Schmitz, Lutz Feld, Andrea Perrotta, Shahram Rahatlou, Janos Erö, Michael Revering, T. R. Fernandez Perez Tomei, A. Romero, S. H. Lee, Julia Velkovska, Sudha Ahuja, Giovanni Mocellin, Robert Hirosky, Giacomo Ortona, J. Taylor, T. Boccali, Riccardo Salvatico, Maurizio Pierini, David Cussans, E. A. De Wolf, Cameron Bravo, Fuqiang Wang, Justin Pilot, Petr Moisenz, David Ja Cockerill, Wolfgang Lange, Erik Gottschalk, Andrea Delgado, Andres Tiko, A. M. Rossi, Halil Saka, Pietro Govoni, Hao Qiu, Claudia Pistone, Wolfgang Adam, Silvia Maselli, Ioannis Papadopoulos, Efstathios Paganis, R. Frühwirth, Erica Brondolin, K. W. Bell, Nataliia Kovalchuk, Dhanush Anil Hangal, Y. Musienko, M. C. Fouz, Samuel Boren, Duncan Leggat, E. Popova, Th. Müller, Candan Isik, Salim Cerci, Amedeo Staiano, Jim Hanlon, D. Soldi, Paul Sheldon, Karl Gill, S. 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Choi, Stephen Sanders, Sridhara Dasu, Emilio Meschi, W. T. Lin, Dylan Hsu, C. Oropeza Barrera, Sioni Summers, Yi-ting Duh, Sumit Keshri, D. Horvath, A. Escalante Del Valle, Boris Grynyov, Giorgia Rauco, Nancy Marinelli, Joosep Pata, Elisa Manoni, Ka Tung Lau, S. Luo, Brieuc Francois, Thomas Madlener, Colin Bernet, Merve Ince, Ugur Kiminsu, G. P. Van Onsem, Giovanni Petrucciani, Martti Raidal, Burin Asavapibhop, Xunwu Zuo, James Bueghly, Matthew Nguyen, V. Rodríguez Bouza, Shengquan Tuo, Pedro G Mercadante, Zviad Tsamalaidze, Nikolai Skatchkov, Vladimir Gavrilov, H. Sert, Hongbo Liao, Aleko Khukhunaishvili, Hans-Christian Kaestli, Mykola Savitskyi, G. L. Pinna Angioni, F. De Guio, Junquan Tao, Pierluigi Paolucci, Andrei Gritsan, Raman Khurana, G. F. Chen, Christopher Rogan, Etiennette Auffray, Maurizio Biasini, D. R. Muller, Yutaro Iiyama, Mehmet Kaya, Intae Yu, Giles Strong, Zuhal Seyma Demiroglu, Zeljko Antunovic, Christoph Paus, P. 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Kleinwort, Xinmei Niu, Marino Missiroli, Dmitry Hits, Jorma Tuominiemi, Gunther Roland, K. El Morabit, Danek Kotlinski, Jordan Martins, A. Melo, Denis Gelé, Catherine Schiber, Mauro Emanuele Dinardo, Carmen Albajar, Sven Dildick, R. D. Field, Dragos Velicanu, Ji Hwan Bhyun, Korbinian Schweiger, E. Eskandari Tadavani, Jack King, R. Vidal, Illia Khvastunov, Li Li, Sudarshan Paramesvaran, Victor Daniel Elvira, Luigi Guiducci, Gregory R Snow, Sarah Freed, Alicia Calderon, Bilal Kiani, Seyed Mohsen Etesami, Sandra Oliveros, Paraskevas Gianneios, Nicolo Cartiglia, F. Hartmann, Stephane Cooperstein, Sivaprasad Mitra, S. Ragazzi, Alfredo Gurrola, Ufuk Guney Tok, Christopher Brew, Gintautas Tamulaitis, Shane Breeze, Iban Jose Cabrillo, Lea Caminada, Rong-Shyang Lu, Igor Volobouev, A. M. Vargas Hernandez, Özlem Özçelik, German Martinez, T. Susa, Cristina Botta, Emanuela Barberis, Anna Kropivnitskaya, P. de Barbaro, Tahereh Sadat Niknejad, Trenton A. Williams, Alberto Santoro, H. S. Kim, Qamar Hassan, I. Heredia-De La Cruz, Nuno Leonardo, Viesturs Veckalns, D. P. Stickland, Vincenzo Daponte, M. Vidal Marono, Andreas Pfeiffer, Alessandra Cappati, Kreso Kadija, Y. C. Yang, Guillaume Falmagne, Julia Thom, Finn Rebassoo, Imad Baptiste Laktineh, Piero Giorgio Verdini, Lucas Taylor, Matthew Citron, G. De Lentdecker, Lin Wang, Ivan Amos Cali, A. Carvalho Antunes De Oliveira, Oliver Pooth, Pallavi Bhat, Ashutosh Bhardwaj, Jan Steggemann, Norbert Neumeister, Andrés Cabrera, Stefano Mersi, Mykyta Haranko, Dario Bisello, Pascal Paganini, Nhan Viet Tran, Mohammad Abrar Wadud, Christof Roland, David Colling, Lothar At Bauerdick, Philip Baringer, Enrico Robutti, George Stephans, Marco Cuffiani, Oliver Buchmuller, Leonardo Giannini, R. Walsh, Amina Zghiche, Jonas Rembser, S. Zhang, Emily MacDonald, Volker Blobel, Aurélien Carle, Geoffrey Smith, Grigory Safronov, Joshua Hardenbrook, Kelly Beernaert, Peter Raics, Peicho Petkov, Yousen Zhang, Silvio Donato, Leonardo Cristella, Harry Cheung, Peter Schleper, Zhen Hu, S. Nandan, A. De Iorio, Pietro Vischia, Francisco Matorras, Hyunyong Kim, Michael Dittmar, Danilo Meuser, Andrew Gilbert, Dipak Kumar Mishra, J. A. Brochero Cifuentes, Simone Bologna, John A Coughlan, Camille Camen, Achille Petrilli, Chun-Hua Jiang, J. Mejia Guisao, Joona Havukainen, Ridhi Chawla, W. Haj Ahmad, Zoltan Laszlo Trocsanyi, Simon Regnard, J. Conway, D. Del Re, Vincent Lemaitre, K. Wichmann, P. Kyberd, Aleksandar Aleksandrov, E. Palencia Cortezon, Vladimir Rusinov, Neeti Parashar, Jacob Linacre, Jiajing Mao, Meenakshi Narain, Mirena Ivova Paneva, Leonid Levchuk, B. Penning, Emanuele Usai, W. T. Hung, Mosayeb Naseri, Luca Scodellaro, Christos Roskas, Maria Cepeda, J. G. Branson, Georg Steinbrück, Barbara Clerbaux, Tariq Aziz, Dave M Newbold, Sushil Chauhan, Kajari Mazumdar, Nickolas Mccoll, Irene Zoi, Cristina Tuve, Thomas Eichhorn, Alessandro Thea, Cristina Fernandez Bedoya, Isabel Pedraza, D. Y. Wang, Marko Dragicevic, A. Di Crescenzo, Jorgen D'Hondt, Paolo Azzurri, Klaus Rabbertz, Emilien Chapon, Sebastiano Albergo, Igor Lokhtin, George Karathanasis, Y. Choi, Brandon Allen, Dustin Burns, C. Scharf, Siarhei Shulha, Vittorio Raoul Tavolaro, I. O. Atakisi, R. G. Kellogg, Alexander Pauls, Prabhat Ranjan Pujahari, Q. Wang, Borislav Pavlov, Vladimir Karjavine, Csaba Hajdu, Emyr Clement, C. Fallon, Kirill Skovpen, L. J. Sanchez Rosas, Urs Langenegger, Davide Piccolo, Davide Fiorina, Paul Baillon, Paolo Gunnellini, Artur Apresyan, Marc Besancon, Dinyar Rabady, Jee-Young Jasmine Choi, Wolfram Dietrich Zeuner, Adrian Byszuk, Pritam Kalbhor, Juliet Ritchie Patterson, Crisostomo Sciacca, Maxim Goncharov, Mario Masciovecchio, Malgorzata Kazana, Marcus Hohlmann, K. Ehataht, Marco Pieri, Christoph Garbers, Huilin Qu, Ian R Tomalin, David Saltzberg, James Letts, T. Mitchell, Bahareh Roozbahani, Nadeesha Wickramage, Anna Zanetti, Q. Ingram, L. Viliani, Zachary Lesko, Troy Mulholland, Seungkyu Ha, Vladimir Palichik, Joao Varela, Sharad Malik, Leander Litov, L. Valencia Palomo, Paul Avery, Salavat Abdullin, Lisa Benato, George Adamov, Caroline Elisabeth Niniane Niemeyer, Y-J Lee, F. L. Fabbri, Daniele Fasanella, D. Green, Marek Gruchala, Alexander Spiridonov, I. A. Melzer-Pellmann, Francesca Nessi-Tedaldi, Jean-Pierre Merlo, Kithsiri Malagalage, Sema Zahid, Yongbin Feng, Bernard Ille, Lalit Mohan Pant, Carlos Florez, Sergei Gleyzer, Ana Ovcharova, Joanne Cole, Aaron Dominguez, Matthias Schröder, Andrea Venturi, M. Khakzad, Ilaria Vai, Rino Castaldi, Ali Mohammadi, Ta-Wei Wang, Brian Dorney, Dinko Ferencek, Quentin Python, Randy Ruchti, Joe Incandela, Luca Cadamuro, Mariarosaria D'Alfonso, Mario Galanti, Zoltan Szillasi, Jussi Viinikainen, Yongho Jeong, A. K. Virdi, Eija Tuominen, Edoardo Bossini, F. Rezaei Hosseinabadi, Andrey Uzunian, Christopher Palmer, Alice Bean, Balazs Ujvari, Nicolas Postiau, Benjamin Krikler, Shervin Nourbakhsh, Marco Musich, S. Belforte, Nabarun Dev, Johan Borg, A. Bermúdez Martínez, Patrick Connor, Min Suk Kim, A. De Cosa, Hannes Sakulin, Andreas Werner Jung, Giovanna Selvaggi, Chandiprasad Kar, Tilman Rohe, Sara Nabili, A. Rossi, Manfred Paulini, Jessica Prisciandaro, Pierluigi Bortignon, Daniel Abercrombie, Kyungwook Nam, Ugo Gasparini, Veikko Karimäki, M. Bluj, Zaixin Wang, Sara Fiorendi, Vasken Hagopian, G. M. Dallavalle, Bhargav Madhusudan Joshi, Georgios Krintiras, Matteo Presilla, Zeynep Demiragli, Marina Kolosova, Yalcin Guler, Gabor Istvan Veres, Roger Wolf, Marina Chadeeva, Lev Dudko, Jeremy Andrea, Laura Dodd, Bobak Hashemi, Andrew Levin, Tom Cornelis, Marta Verweij, Sarah Catherine Eno, Jan-Frederik Schulte, Hong Ni, W. T. Ford, P. J. Fernández Manteca, Luca Guzzi, Felicitas Pauss, Pierluigi Zotto, Hwi Dong Yoo, Anton Stepennov, Andrew Loeliger, Robert Bainbridge, Ashley Parker, Shivali Malhotra, Tanmay Mudholkar, Ennio Monteil, Aldo Penzo, Vladislav Borchsh, Pieter Everaerts, Giovanni Franzoni, Evrim Ersin Kangal, Ashok Kumar, A. García Alonso, D. H. Miller, Anadi Canepa, Nicolas Tonon, Artur Gottmann, Aimilios Ioannou, Filippo Errico, Deepak Kumar Sahoo, Jean-Louis Faure, Philipp Millet, Dario Menasce, Brian Francis, Tamas Ferenc Csorgo, Simranjit Singh Chhibra, Matteo Cremonesi, Angira Rastogi, Paolo Checchia, Nitish Dhingra, J. Suarez Gonzalez, Titas Roy, Alberto Messineo, John Almond, Alexx Perloff, Roman Ryutin, Federica Primavera, Roberto Carlin, Pierre Depasse, Vyacheslav Klyukhin, M. Van De Klundert, Victor Golovtcov, Rachael Bucci, You-ying Li, Samuel Bein, Luisa Benussi, Daniel Spitzbart, Richard B. Lipton, Nicholas Eminizer, Daniele Ruini, Ali Eren Simsek, Eric Conte, David Barney, Aleksandra Lelek, Stephanie Beauceron, Michail Bachtis, Ulrich Husemann, A. Manousakis-Katsikakis, Fabio Monti, J. G. Li, Roberto Rossin, Siew Yan Hoh, Alexander Ershov, Bennett Marsh, Duncan Carlsmith, Austin Baty, Kristian Harder, Ravindra Kumar Verma, E. Belchior Batista Das Chagas, D. Pérez Adán, Shin-Shan Yu, Wenxing Fang, Geoffrey Hall, William Mcbrayer, S. Bhattacharya, Rizki Syarif, Ia Iashvili, G. N. Kim, Georgios Tsipolitis, Sanjay Padhi, Jean-Roch Vlimant, Brajesh C Choudhary, Paul David Luckey, Marco Trovato, Sébastien Viret, Mia Tosi, Anne Dabrowski, Bryan Caraway, T. Y. Ling, D. Cutts, W. Snoeys, Michael Benjamin Andrews, Simone Paoletti, Abhijith Gandrakota, B. Chazin Quero, L. Romero, Prashant Shukla, André Rosowsky, Andrew Ivanov, Suchandra Dutta, J. A. Murillo Quijada, Panagiotis Kokkas, Giulio Mandorli, S. Sarkar, S. K. Pflitsch, Anne-Marie Magnan, Wagner Carvalho, Niels Dupont, Zhengcheng Tao, Gy L. Bencze, J. M. Hernandez, Edward Laird, Aurore Savoy-Navarro, Luca Mastrolorenzo, P. E. Karchin, David Yu, P. D. Dauncey, A. Castro, Vieri Candelise, Ted Kolberg, C. Uribe Estrada, Muhammad Shoaib, Claude Charlot, Reddy Pratap Gandrajula, P. Rebello Teles, Amandeep Kaur Kalsi, Leonard Spiegel, Francesco Romeo, Robert Klanner, Paolo Giacomelli, Andrea Benaglia, Fabio Cossutti, Joachim Mnich, Andreas Mussgiller, Valerio Bertacchi, Tobias Pook, Jay Hauser, A. Vilela Pereira, Fotios Ptochos, Riccardo Bellan, Christophe Royon, Elizabeth Sexton-Kennedy, Bobae Kim, Matthias Wolf, Suresh C Tonwar, Sylvie Braibant-Giacomelli, Jeffrey Roskes, Kalliopi Manitara, Paolo Ronchese, Badder Marzocchi, Sanjay Kumar Swain, Greg Landsberg, Cécile Caillol, Sw. Banerjee, Claudio Grandi, Sébastien Gadrat, Mayda Velasco, Manjit Kaur, M. Melo De Almeida, Darin Acosta, Kristian Allan Hahn, Marc M Baarmand, Daniele Trocino, A. Stahl, Ian Laflotte, C. Mills, Winston Ko, I. De Bruyn, Reza Goldouzian, Mohd Nizam Yusli, Kenichi Hatakeyama, Anna Woodard, Petr Levchenko, Nikolai Golubev, Renato Potenza, D. R. Claes, Marcel Rieger, Anders Ryd, Gavin Davies, Anna Colaleo, M. Voutilainen, Wing Yan Wong, Yildiray Komurcu, Guenter Eckerlin, Alexander Lanev, T. Kress, Susan Dittmer, Georgios Daskalakis, Sergei Gninenko, J. C. Freeman, Petr Mandrik, M. Shi, Senka Duric, Benjamin Tannenwald, Guler Karapinar, Samuel May, Armen Tumasyan, Giuseppe Latino, Paula Eerola, S. Fonseca De Souza, D. S. Lemos, Manoj Sharan, Matthew Kilpatrick, Alessandro Giassi, Süleyman Durgut, John Paul Chou, J. L. Dulemba, S. Somalwar, Rishabh Uniyal, C. E. Flores, Rui Xiao, Brian Paul Padley, Justin Williams, Simone Pigazzini, Zhaozhong Shi, Nairit Sur, S. Slabospitskii, Pedrame Bargassa, Gregory Iles, Nikolay Voytishin, K. H. M. Kwok, C. F. González Hernández, Markus Stoye, Kevin Burkett, Kira Burt, James Keaveney, C. Wissing, A. Castaneda Hernandez, Constantin Heidegger, Yuri Skovpen, Natasa Raicevic, A. Di Mattia, Gianni Zumerle, Ivan Vila, S. Carrillo Moreno, Sunil Bansal, Nicholas Smith, Zehui Zhang, Eleni Erodotou, William John Womersley, Jean-Charles Fontaine, Anton Dimitrov, Luciano Di Fiore, Andrea Gozzelino, Werner Lustermann, Andromachi Tsirou, James Strait, Daniele Bonacorsi, Nicholas Haubrich, Aleksandr Iuzhakov, A. Moraes, Tomas Lindén, N. Van Remortel, M. Bharti, V. Sola, A. Baden, M. Barrio Luna, Alice Florent, R. Di Maria, P. Martinez Ruiz del Arbol, Fabio Iemmi, Dan Quach, G. P. Siroli, Ricardo Lopez-Fernandez, Bhumika Kansal, Andrea Triossi, Christoph Schwick, M. Aguilar-Benitez, Leszek Grzanka, Rylan Conway, J. F. de Trocóniz, J. Vaitkus, V. Myronenko, Alexander Toropin, Simone Gennai, Matthias Ulrich Mozer, Svenja Schumann, Rami Kamalieddin, M. P. Rauch, Bibhuprasad Mahakud, G. Gomez Ceballos, A. Morelos Pineda, Daniel Rosenzweig, Geum Bong Yu, Evan Ranken, S. B. Oh, Alexander Malakhov, Günter Flügge, Nikos Varelas, Helen F Heath, Joshua Hiltbrand, Danyyl Brzhechko, M. Naimuddin, Tyler Ruggles, Alexis Pompili, Abraham Tishelman-Charny, Stephen Wimpenny, Henning Flacher, Robert Clare, Lucas Torterotot, Patrizia Azzi, Thomas Hebbeker, Paul Lecoq, Bruno Lenzi, Nikolaos Manthos, Martin Grunewald, J. Piedra Gomez, Wolfram Erdmann, A. De Roeck, A. J. Campbell, A. David, Ksenia Shchelina, Albert M. Sirunyan, K. Vellidis, E. Di Marco, Gaël Touquet, Rajat Gupta, Mara Senghi Soares, Serguei Ganjour, Jeremi Niedziela, Chiara Amendola, A. Di Florio, Silvia Taroni, Maria Giulia Ratti, A. De Wit, Frans Meijers, Stephen Trembath-Reichert, Hessamoddin Kaveh, Edward Scott, Darien Wood, Jyothsna Rani Komaragiri, Ian Watson, Nicholas John Hadley, Jehad Mousa, Karl Matthew Ecklund, A. Rizzi, Maral Alyari, A. Richards, Duje Giljanovic, J. Park, Caleb Fangmeier, Vinicius Massami Mikuni, D. R. Mendis, Igor Vorobiev, Martin Delcourt, Francesco Fallavollita, Julie Managan Hogan, Panos A Razis, John Gabriel Acosta, Paul Lujan, Nadja Strobbe, Jean-Laurent Agram, G. Paspalaki, Anthony Moeller, I. Dremin, P. De Castro Manzano, Anthony Lefeld, Aristotelis Kyriakis, Welathantri Gd Dharmaratna, Ferenc Sikler, Mauro Verzetti, Mario Kadastik, Alexander Dermenev, Seth Cooper, Semra Turkcapar, Linda Finco, Mingshui Chen, Matthias Komm, Arnab Purohit, Wei Zhang, Simona Cometti, Scott Thomas, S. W. Lee, J. D. Richman, Yannik Rath, Predrag Cirkovic, Viola Sordini, Erika Garutti, Giancarlo Mantovani, Carlo Battilana, Sezen Sekmen, Z. Liu, Inseok Yoon, S. Consuegra Rodríguez, K. Osterberg, Maximilian Heindl, Alexander Savin, M. Finger, Minseok Oh, Andrés G Delannoy, Christopher Hill, Dong Ho Moon, Adam Elwood, Sami Lehti, Adish Vartak, David Bertsche, Valentina Mariani, Ivan Shvetsov, Igor Golutvin, Mircho Rodozov, Jennifer Ngadiuba, Prasant Kumar Rout, Á. Navarro Tobar, Nicola Bacchetta, Attila Racz, Roberta Arcidiacono, Christian Schnaible, Jonathan Fulcher, Anatoli Pashenkov, Avto Kharchilava, Mikhail Ignatenko, Tapio Lampén, Riccardo Paramatti, Andrea Giammanco, Priyanka Kumari, Norraphat Srimanobhas, Dermot Moran, W. A. T. Wan Abdullah, Jamal Rorie, Jason Gilmore, Marco Paganoni, Don Lincoln, Li Yuan, W. De Boer, Jory Sonneveld, Hafeez R Hoorani, Alessandro Cardini, Daniel John Karmgard, Manfred Jeitler, Fabrizio Palla, Owen Baron, Vivekanand Jha, Steve Schnetzer, Saranya Ghosh, Klaas Padeken, Renato Campanini, Rosamaria Venditti, W. J. Metzger, Carlos Lourenco, Najaf Amin, A. Braghieri, Luca Perrozzi, Manfred Krammer, Kevin Sung, Konstanty Sumorok, Maria Savina, Adel Terkulov, Caglar Zorbilmez, P. C. Tiwari, Emrah Tiras, Toyoko Orimoto, Bolek Wyslouch, Maria Spiropulu, Christian Dorfer, Matthew Herndon, Elisa Fontanesi, Thomas James, Sevgi Tekten, Jovan Milosevic, Vitaliano Ciulli, Apostolos Panagiotou, Benjamin Kilminster, Benjamin Fischer, Aniello Spiezia, Christopher West, Jonas Roemer, Zhoudunming Tu, Isabel Ojalvo, Youn Roh, Barry Blumenfeld, T. V. Dimova, Rachel Yohay, J. K. Lim, F. Simonetto, Sergio P Ratti, Frank Chlebana, Kuntal Mondal, Giovanni Organtini, Alessia Saggio, Paolo Spagnolo, P. Gras, W. Ji, Claudio Quaranta, Lindsey Gray, Alberto Belloni, Piet Verwilligen, Jan Eysermans, Attilio Santocchia, Jean Fay, A. B. Meyer, Burak Bilki, Nicolò Trevisani, Dirk Krücker, Gianluca Cerminara, Lorenzo Russo, Rostyslav Shevchenko, Patrick Asenov, M. Weber, Aruna Nayak, J. H. Yoo, Gervasio Gomez, A. Delgado Peris, Rohan Bhandari, Vinay Hegde, David Zou, Finn Feindt, Andrey Korytov, P. Chang, Eduardo De Moraes Gregores, Ashfaq Ahmad, Ashim Roy, Andre Frankenthal, Jan Krolikowski, Luiz Mundim, C.-E. Wulz, Duccio Abbaneo, Elizabeth Locci, Cristina Biino, Gabriele Benelli, Patrizia Barria, Somnath Choudhury, L. V. Kardapoltsev, Amitabh Lath, Simon Kudella, Angela Mehta, C. Martinez Rivero, Giorgio Apollinari, Ulf Behrens, M. A. Shah, Benjamin Mesic, F. Pandolfi, Teruki Kamon, James Buchanan, Maxim Pieters, A. Di Francesco, Ulrich Heintz, M. Kovac, Bjorn Burkle, N. Vanegas Arbelaez, Erhan Gülmez, Kaori Maeshima, Aurelijus Rinkevicius, Martin Erdmann, Andrew Wisecarver, Patricia McBride, Krzysztof Doroba, Dylan Rankin, Andrew Brinkerhoff, Thomas Ferguson, Jose Flix, Didier Contardo, Gregor Kasieczka, Y. Chao, Lesya Shchutska, Andrea Massironi, Raffaella Radogna, Markéta Jansová, Francesco Navarria, Sotiroulla Konstantinou, Christopher George Tully, Alexander Belyaev, Claudio Campagnari, Teppo Mäenpää, Stephanie Brandt, R. Mankel, Wolfgang Lohmann, Filip Moortgat, Konstantinos Kousouris, Arne Reimers, Joshua Bendavid, Nicanor Colino, F. Mohamad Idris, Malte Backhaus, and Nicholas Wardle
Subjects: Quark, Physics, Nuclear and High Energy Physics, Luminosity (scattering theory), Proton, 010308 nuclear & particles physics, Dark matter, Resonance, 01 natural sciences, Nuclear physics, 0103 physical sciences, High Energy Physics::Experiment, Invariant mass, 010306 general physics, Event (particle physics), Boson
Abstract: A search for a narrow resonance with a mass between 350 and 700 GeV, and decaying into a pair of jets, is performed using proton-proton collision events containing at least three jets. The data sample corresponds to an integrated luminosity of 18.3 fb(-1) recorded at root s = 13 TeV with the CMS detector. Data are collected with a technique known as "data scouting", in which the events are reconstructed, selected, and recorded at a high rate in a compact form by the high-level trigger. The three-jet final state provides sensitivity to lower resonance masses than in previous searches using the data scouting technique. The spectrum of the dijet invariant mass, calculated from the two jets with the largest transverse momenta in the event, is used to search for a resonance. No significant excess over a smoothly falling background is found. Limits at 95% confidence level are set on the production cross section of a narrow dijet resonance and compared with the cross section of a vector dark matter mediator coupling to dark matter particles and quarks. Translating to a model where the narrow resonance interacts only with quarks, upper limits on this coupling range between 0.10 and 0.15, depending on the resonance mass. These results represent the most stringent upper limits in the mass range between 350 and 450 GeV obtained with a flavor-inclusive dijet resonance search. (C) 2020 The Author(s). Published by Elsevier B.V.
Published: 2020
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36. An efficient synthesis of triazolium ion based NHC precursors using diaryliodonium salts and their photophysical properties

Author: V. Arun, Sivaprasad Mitra, Manish Kumar Mehra, Mostofa Ataur Rohman, Meenakshi Pilania, and Dalip Kumar
Subjects: chemistry.chemical_classification, Aqueous medium, 010405 organic chemistry, Chemistry, Aryl, Organic Chemistry, 010402 general chemistry, 01 natural sciences, Biochemistry, Combinatorial chemistry, Fluorescence, 0104 chemical sciences, Ion, chemistry.chemical_compound, Halogen, Nitro, Physical and Theoretical Chemistry, Benzoin condensation, Alkyl
Abstract: Copper-catalysed N-arylation of fused triazoles using diaryliodonium salts as an aryl source is described. This scalable protocol displayed good compatibility towards diverse sensitive functional groups like ester, alkyl and nitro groups and halogens (F, Cl, Br). The synthetic usefulness of the prepared triazolium salts was proved by preparing α-hydroxyketone through benzoin condensation. Photophysical studies of these compounds showed promising Stokes-shifted fluorescence emission in aqueous medium, so this molecular framework could be a proficient probe for biological applications.
Published: 2018

37. Quenching of Luminol Fluorescence at Nano-Bio Interface: Towards the Development of an Efficient Energy Transfer System

Author: Vikash K. Sonu and Sivaprasad Mitra
Subjects: Silver, Sociology and Political Science, Clinical Biochemistry, Nanoparticle, Metal Nanoparticles, 010402 general chemistry, Photochemistry, 01 natural sciences, Biochemistry, Fluorescence, Luminol, chemistry.chemical_compound, Nano, Animals, Bovine serum albumin, Spectroscopy, Quenching (fluorescence), Luminescent Agents, biology, 010405 organic chemistry, Chemistry, Serum Albumin, Bovine, Acceptor, 0104 chemical sciences, Clinical Psychology, Energy Transfer, Colloidal gold, biology.protein, Cattle, Gold, Law, Social Sciences (miscellaneous)
Abstract: Surface modified colloidal gold (Au) and silver (Ag) nanoparticles (NPs) were used as efficient quenchers of luminol (LH2) fluorescence either in homogeneous aqueous medium or its noncovalent assembly with bovine serum albumin (BSA). The mechanism as well as the extent of fluorescence quenching was found to be strongly dependent on the nature of the nanoparticles. While simple static type fluorescence quenching mechanism was perceived with AuNP, a more complex protocol involving quenching sphere model was envisaged for AgNP quenching. Nevertheless, the magnitude of Stern-Volmer (SV) quenching constant (KSV ~ 108–1010 M−1) was calculated to be ca. 104 times more for surface quoted NPs in comparison with BSA–NP bioconjugates system. On the other hand, a highly efficient (E ≈ 95%) energy transfer (ET) process was predicted for LH2 captured in the hydrophobic assembly with BSA in presence of AgNP as an acceptor. The ET efficiency is critically dependent on the concentration of BSA and nicely correlated with the extent of NP surface coverage. However, fluorescence quenching on AuNP surface is relatively less responsive towards protein concentration, primarily due to the difference in surface activity as well as the mode of interaction of the protein with NPs.
Published: 2018

38. Novel coumarin derivatives as potent acetylcholinesterase inhibitors: insight into efficacy, mode and site of inhibition

Author: Semen O. Yesylevskyy, Kripamoy Aguan, Prayasee Baruah, Grace Basumatary, Sivaprasad Mitra, and Ghanashyam Bez
Subjects: Models, Molecular, Aché, 030303 biophysics, Inhibitory postsynaptic potential, Catalysis, 03 medical and health sciences, chemistry.chemical_compound, Structure-Activity Relationship, Structural Biology, Coumarins, medicine, Humans, heterocyclic compounds, Molecular Biology, chemistry.chemical_classification, 0303 health sciences, Binding Sites, Molecular Structure, Hydrolysis, General Medicine, Coumarin, Human serum albumin, Acetylcholinesterase, language.human_language, Enzyme, chemistry, Biochemistry, Aqueous buffer, language, Cholinesterase Inhibitors, medicine.drug, Protein Binding
Abstract: The inhibitory efficacy of two substituted coumarin derivatives on the activity of neurodegenerative enzyme acetylcholinesterase (AChE) was assessed in aqueous buffer as well as in the presence of human serum albumin (HSA) and compared against standard cholinergic AD drug, Donepezil (DON). The experimental data revealed the inhibition to be of non-competitive type with both the systems showing substantial inhibitory activity on AChE. In fact, one of the tested compounds Chromenyl Coumarate (CC) was found to be better inhibitor (IC50 = 48.49 ± 5.6 nM) than the reference drug DON (IC50 = 74.13 ± 8.3 nM), unequivocally amplifying its importance. The structure of the compound was found to play a vital role in the inhibitory efficiency, validating previous Structure Activity Relationship (SAR) reviews for coumarin. The mechanism of inhibition remained impervious when the experimental medium was switched from aqueous buffer to HSA, albeit noticeable change in the inhibition potency of the compound 3, 3′- Methylene-bis (4-hydroxy coumarin) (MHC) (38%) and CC (35%). Both the coumarin derivatives were observed to bind to the peripheral anionic site (PAS) of AChE and also found to displace the fluorescence marker thioflavinT (ThT) from AChE binding pocket. All experimental observations were seconded by molecular docking and MD simulation results. The inferences drawn in this study form a foundation for further investigation on these compounds; magnifying the probability of their usage as AD drugs and re-emphasizes the significance of drug delivery media while considering the inhibition potencies of targeted drugs.
Published: 2018

39. Interaction of caffeine and sulfadiazine with lysozyme adsorbed at colloidal metal nanoparticle interface: influence on drug transport ability and antibacterial activity

Author: Vikash K. Sonu, Sivaprasad Mitra, Kaushik Bhattacharjee, Imocha Rajkumar, and Santa Ram Joshi
Subjects: Silver, Molecular Conformation, Nanoparticle, Metal Nanoparticles, Sulfadiazine, Molecular Dynamics Simulation, 010402 general chemistry, 01 natural sciences, Metal, chemistry.chemical_compound, Colloid, Adsorption, Structural Biology, Caffeine, 0103 physical sciences, medicine, Colloids, Molecular Biology, Drug Carriers, 010304 chemical physics, Chemistry, Temperature, General Medicine, Models, Theoretical, Enzymes, Immobilized, Combinatorial chemistry, 0104 chemical sciences, Anti-Bacterial Agents, Molecular Docking Simulation, visual_art, visual_art.visual_art_medium, Thermodynamics, Muramidase, Gold, Lysozyme, Antibacterial activity, Algorithms, medicine.drug
Abstract: The modulated bioactivity of proteins immobilized on nanoparticle (NP) interfaces is of tremendous interest toward designing better therapeutic and diagnostic tools. In this work, binding behavior and the antibacterial activity of free lysozyme (LYS) as well as its non-covalent assembly with silver (Ag) and gold (Au) colloidal NPs were compared in presence of two model drugs, viz. sulfadiazine (SDZ) and caffeine (CAF). Intrinsic protein fluorescence was found to quench due to the formation drug–protein complex in case of CAF resulting a linear Stern–Volmer (SV) plot with KSV = 1.83 × 103 M−1.On the other hand, a positive deviation beyond [SDZ] ~0.15 mM is explained due to the formation of a fluorophore – quencher sphere with radius of 13.85 ± 1.80 Å that results almost one order of magnitude higher KSV (1.75 × 104 M−1). Molecular docking calculation also predicts relatively more stabilized complex of SDZ with LYS in comparison to CAF (ΔE ~ 3 kJ mol−1). Synchronous fluorescence results corresponding to Trp and Tyr residues as well as FTIR spectra in the amide I region of LYS confirms minimal deformation in the LYS secondary structure on adsorption to spherical NP surface. Although the nature of LYS–drug interaction remains invariant, the extent of quenching interaction as well as the drug binding ability is strongly modulated in presence of NPs. Further, the antibacterial activity of LYS in presence of the investigated drugs shows 9–14% upsurge with AuNP, in sharp contrast to ca. 31–34% decrease in AgNP.
Published: 2018

40. Search for Zγ resonances using leptonic and hadronic final states in proton-proton collisions at $ \sqrt{s}=13 $ TeV

Author: Andreas Künsken, Laurent Thomas, Mark Derdzinski, Pushpalatha C Bhat, Rachel Yohay, J. K. Lim, F. Simonetto, Andreas Hinzmann, Marcin Konecki, Artur Lobanov, Nathaniel Pastika, Alexis Pompili, Sergio P Ratti, Victor Murzin, Frank Chlebana, Kuntal Mondal, Giovanni Organtini, Kyle Tos, L. J. Gutay, David Curry, Adrian Perieanu, A. Meyer, Russell Richard Betts, Q. Li, Miaoyuan Liu, Tutanon Sinthuprasith, Alessia Saggio, Paolo Spagnolo, P. Gras, Andreas Psallidas, C. Vander Velde, E. Carrera Jarrin, Stefan Michael Heindl, W. Ji, Swapan Kumar Sarkar, Ioannis Evangelou, Geonhee Oh, Lisa Borgonovi, A. A. Bin Anuar, Damir Lelas, Lindsey Gray, Serhat Atay, Louie Corpe, Stephen Wimpenny, Henning Flacher, Nikolaos Manthos, Conor Henderson, Prasenjit Mal, Christina Snyder, Konstantin Matchev, J. J. Hollar, Jean-Marie Brom, Igor Bayshev, Xavier Coubez, C. Neu, Katja Klein, Alberto Belloni, Piet Verwilligen, Giles Strong, P. Van Hove, Alice Cocoros, R. F. Harr, A. Baden, Gregor Mittag, Evgueni Vlasov, Jan Eysermans, Attilio Santocchia, Jean Fay, Panagiotis Katsoulis, Stephen Mrenna, Denys Lontkovskyi, Roberto Sacchi, Tejinder Virdee, Nicolò Tosi, Christian Laner, Martin Grunewald, J. Piedra Gomez, Fabrice Couderc, Alex Garabedian, Egidio Longo, Olga Driga, Giacomo Sguazzoni, Javier Duarte, Alexandre Zabi, Vladimir Rekovic, V. Andreev, Francesco Fienga, Roy Montalvo, Federico Preiato, Oleg Prokofyev, Wolfram Erdmann, Francesca Ricci-Tam, T. du Pree, Igor Dremin, Abideh Jafari, Rogelio Reyes-Almanza, Nathan Mirman, Jennifer Chu, J. H. Kim, M. Jones, Camilla Galloni, Seth Conrad Zenz, A. B. Meyer, Mara Senghi Soares, Serguei Ganjour, Silvia Taroni, Ahmad Borzou, Ivan Marchesini, Mohsan Waseem Ather, Anna Stakia, Sébastien Wertz, Gino Bolla, M. Barrio Luna, P. Martinez Ruiz del Arbol, Burak Bilki, Marc Weinberg, Viktor Khristenko, Gaël Perrin, Salvatore Rappoccio, Dan Quach, S. M. A. Ghiasi Shirazi, Igor Miagkov, Marino Missiroli, C. 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Paktinat Mehdiabadi, Fatma Boran, CMS Collaboration, Özdemir, Kadri, Yerevan Phys Inst, Inst Hochenergiephys, Inst Nucl Problems, Univ Antwerp, Vrije Univ Brussel, Univ Libre Bruxelles, Univ Ghent, Catholic Univ Louvain, Ctr Brasileiro Pesquisas Fis, Universidade do Estado do Rio de Janeiro (UERJ), Universidade Estadual Paulista (Unesp), Universidade Federal do ABC (UFABC), Bulgarian Acad Sci, Univ Sofia, Beihang Univ, Inst High Energy Phys, Peking Univ, Tsinghua Univ, Univ Los Andes, Univ Split, Inst Rudjer Boskovic, Univ Cyprus, Charles Univ Prague, Univ San Francisco Quito, Acad Sci Res & Technol Arab Republ Egypt, NICPB, Univ Helsinki, Helsinki Inst Phys, Lappeenranta Univ Technol, Univ Paris Saclay, Univ Strasbourg, CNRS, Univ Claude Bernard Lyon 1, Georgian Tech Univ, Tbilisi State Univ, Rhein Westfal TH Aachen, DESY, Univ Hamburg, Inst Expt Kernphys, NCSR Demokritos, Univ Athens, Natl Tech Univ Athens, Univ Ioannina, Eotvos Lorand Univ, Wigner Res Ctr Phys, Inst Nucl Res ATOMKI, Univ Debrecen, Indian Inst Sci IISc, Natl Inst Sci Educ & Res, Panjab Univ, Univ Delhi, HBNI, Indian Inst Technol, Bhabha Atom Res Ctr, Tata Inst Fundamental Res A, Tata Inst Fundamental Res B, IISER, Inst Res Fundamental Sci IPM, Univ Coll Dublin, INFN, Univ Bari, Politecn Bari, Univ Bologna, Univ Catania, Univ Firenze, Univ Genoa, Univ Milano Bicocca, Univ Napoli Federico II, Univ Basilicata, Univ G Marconi, Univ Padua, Univ Trento, Univ Pavia, Univ Perugia, Univ Pisa, Scuola Normale Super Pisa, Sapienza Univ Roma, Univ Turin, Univ Piemonte Orientale, Univ Trieste, Kyungpook Natl Univ, Chonbuk Natl Univ, Chonnam Natl Univ, Hanyang Univ, Korea Univ, Seoul Natl Univ, Univ Seoul, Sungkyunkwan Univ, Vilnius Univ, Univ Malaya, IPN, Univ Iberoamer, Benemerita Univ Autonoma Puebla, Univ Autonoma San Luis Potosi, Univ Auckland, Univ Canterbury, Quaid I Azam Univ, Natl Ctr Nucl Res, Univ Warsaw, Lab Instrumentacao & Fis Expt Particulas, Joint Inst Nucl Res, Petersburg Nucl Phys Inst, Inst Nucl Res, Inst Theoret & Expt Phys, Moscow Inst Phys & Technol, Natl Res Nucl Univ, PN Lebedev Phys Inst, Lomonosov Moscow State Univ, NSU, Univ Belgrade, Ctr Invest Energet Medioambientales & Tecnol CIEM, Univ Autonoma Madrid, Univ Oviedo, Univ Cantabria, European Org Nucl Res, Paul Scherrer Inst, Swiss Fed Inst Technol, Univ Zurich, Natl Cent Univ, NTU, Chulalongkorn Univ, Cukurova Univ, Middle East Tech Univ, Bogazici Univ, Istanbul Tech Univ, Natl Acad Sci Ukraine, Kharkov Inst Phys & Technol, Univ Bristol, Rutherford Appleton Lab, Imperial Coll, Brunel Univ, Baylor Univ, Catholic Univ Amer, Univ Alabama, Boston Univ, Brown Univ, Univ Calif Davis, Univ Calif Los Angeles, Univ Calif Riverside, Univ Calif San Diego, Univ Calif Santa Barbara, CALTECH, Carnegie Mellon Univ, Univ Colorado, Cornell Univ, Fermilab Natl Accelerator Lab, Univ Florida, Florida Int Univ, Florida State Univ, Florida Inst Technol, UIC, Univ Iowa, Johns Hopkins Univ, Univ Kansas, Kansas State Univ, Lawrence Livermore Natl Lab, Univ Maryland, MIT, Univ Minnesota, Univ Mississippi, Univ Nebraska, SUNY Buffalo, Northeastern Univ, Northwestern Univ, Univ Notre Dame, Ohio State Univ, Princeton Univ, Univ Puerto Rico, Purdue Univ, Purdue Univ Northwest, Rice Univ, Univ Rochester, Rockefeller Univ, Rutgers State Univ, Univ Tennessee, Texas A&M Univ, Texas Tech Univ, Vanderbilt Univ, Univ Virginia, Wayne State Univ, Univ Wisconsin, Vienna Univ Technol, Universidade Estadual de Campinas (UNICAMP), Univ Fed Pelotas, Ain Shams Univ, British Univ Egypt, Zewail City Sci & Technol, Univ Haute Alsace, Brandenburg Tech Univ Cottbus, Indian Inst Technol Bhubaneswar, Inst Phys, Univ Visva Bharati, Univ Ruhuna, Isfahan Univ Technol, Yazd Univ, Islamic Azad Univ, Univ Siena, Int Islamic Univ Malaysia, MOSTI, Consejo Nacl Ciencia & Technol, Warsaw Univ Technol, St Petersburg State Polytech Univ, Budker Inst Nucl Phys, Scuola Normale, Sezione Ist Nazl Fis Nucl, Riga Tech Univ, Stefan Meyer Inst Subatom Phys, Istanbul Aydin Univ, Mersin Univ, Cag Univ, Piri Reis Univ, Gaziosmanpasa Univ, Adiyaman Univ, Izmir Inst Technol, Necmettin Erbakan Univ, Marmara Univ, Kafkas Univ, Istanbul Bilgi Univ, Univ Southampton, Inst Astrofis Canarias, Utah Valley Univ, Beykent Univ, Bingol Univ, Erzincan Univ, Sinop Univ, Mimar Sinan Univ, Texas A&M Univ Qatar, Sirunyan, Albert M, Lista, Luca, Iorio, Alberto O M, And, Others, Massachusetts Institute of Technology. Department of Physics, Abercrombie, Daniel Robert, Allen, Brandon Leigh, Azzolini, Virginia, Barbieri, Richard Alexander, Baty, Austin Alan, Bi, Ran, Brandt, Stephanie Akemi, Busza, Wit, Cali, Ivan Amos, D'Alfonso, Mariarosaria, Gomez-Ceballos, Guillelmo, Goncharov, Maxim, Hsu, Dylan George, Hu, Miao, Iiyama, Yutaro, Innocenti, Gian Michele, Klute, Markus, Kovalskyi, Dmytro, Lee, Yen-Jie, Levin, Andrew Michael, Luckey Jr, P David, Maier, Benedikt, Marini, Andrea Carlo, McGinn, Christopher Francis, Mironov, Camelia Maria, Narayanan, Siddharth Madhavan, Niu, Xinmei, Paus, Christoph M. E., Roland, Christof E, Roland, Gunther M, Salfeld-Nebgen, Jakob Maxillian Henry, Stephans, George S. F., Tatar, Kaya, Velicanu, Dragos Alexandru, Wang, J., Wang, Ta-Wei, Wyslouch, Boleslaw, Institut de Recherches sur les lois Fondamentales de l'Univers (IRFU), Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Université Paris-Saclay, Laboratoire Leprince-Ringuet (LLR), Centre National de la Recherche Scientifique (CNRS)-École polytechnique (X)-Institut National de Physique Nucléaire et de Physique des Particules du CNRS (IN2P3), Institut Pluridisciplinaire Hubert Curien (IPHC), Institut National de Physique Nucléaire et de Physique des Particules du CNRS (IN2P3)-Université de Strasbourg (UNISTRA)-Centre National de la Recherche Scientifique (CNRS), Université de Haute-Alsace (UHA) Mulhouse - Colmar (Université de Haute-Alsace (UHA)), Centre de Calcul de l'IN2P3 (CC-IN2P3), Institut National de Physique Nucléaire et de Physique des Particules du CNRS (IN2P3)-Centre National de la Recherche Scientifique (CNRS), Institut de Physique Nucléaire de Lyon (IPNL), Centre National de la Recherche Scientifique (CNRS)-Université Claude Bernard Lyon 1 (UCBL), Université de Lyon-Université de Lyon-Institut National de Physique Nucléaire et de Physique des Particules du CNRS (IN2P3), CMS, Belforte, S., Candelise, V., Casarsa, M., Cossutti, F., DELLA RICCA, G., Zanetti, A., ET AL (the CMS, Collaboration), Izmir Institute of Technology. Mathematics, Institut National de Physique Nucléaire et de Physique des Particules du CNRS (IN2P3)-École polytechnique (X)-Centre National de la Recherche Scientifique (CNRS), Université de Strasbourg (UNISTRA)-Université de Haute-Alsace (UHA) Mulhouse - Colmar (Université de Haute-Alsace (UHA))-Institut National de Physique Nucléaire et de Physique des Particules du CNRS (IN2P3)-Centre National de la Recherche Scientifique (CNRS), Université Claude Bernard Lyon 1 (UCBL), Université de Lyon-Université de Lyon-Institut National de Physique Nucléaire et de Physique des Particules du CNRS (IN2P3)-Centre National de la Recherche Scientifique (CNRS), Department of Physics, Helsinki Institute of Physics, Elementary Particle Physics, Physics, Faculty of Sciences and Bioengineering Sciences, Vriendenkring VUB, Université de Strasbourg (UNISTRA)-Centre National de la Recherche Scientifique (CNRS), Centre National de la Recherche Scientifique (CNRS)-Institut National de Physique Nucléaire et de Physique des Particules du CNRS (IN2P3), Sirunyan, A, Tumasyan, A, Adam, W, Ambrogi, F, Asilar, E, Bergauer, T, Brandstetter, J, Brondolin, E, Dragicevic, M, Ero, J, Escalante Del Valle, A, Flechl, M, Friedl, M, Fruhwirth, R, Ghete, V, Grossmann, J, Hrubec, J, Jeitler, M, Konig, A, Krammer, N, Kratschmer, I, Liko, D, Madlener, T, Mikulec, I, Pree, E, Rad, N, Rohringer, H, Schieck, J, Schofbeck, R, Spanring, M, Spitzbart, D, Waltenberger, W, Wittmann, J, Wulz, C, Zarucki, M, Chekhovsky, V, Mossolov, V, Suarez Gonzalez, J, De Wolf, E, Di Croce, D, Janssen, X, Lauwers, J, Van De Klundert, M, Van Haevermaet, H, Van Mechelen, P, Van Remortel, N, Abu Zeid, S, Blekman, F, D'Hondt, J, De Bruyn, I, De Clercq, J, Deroover, K, Flouris, G, Lontkovskyi, D, Lowette, S, Marchesini, I, Moortgat, S, Moreels, L, Python, Q, Skovpen, K, Tavernier, S, Van Doninck, W, Van Mulders, P, Van Parijs, I, Beghin, D, Bilin, B, Brun, H, Clerbaux, B, De Lentdecker, G, Delannoy, H, Dorney, B, Fasanella, G, Favart, L, Goldouzian, R, Grebenyuk, A, Lenzi, T, Luetic, J, Maerschalk, T, Marinov, A, Seva, T, Starling, E, Vander Velde, C, Vanlaer, P, Vannerom, D, Yonamine, R, Zenoni, F, Zhang, F, Cimmino, A, Cornelis, T, Dobur, D, Fagot, A, Gul, M, Khvastunov, I, Poyraz, D, Roskas, C, Salva, S, Tytgat, M, Verbeke, W, Zaganidis, N, Bakhshiansohi, H, Bondu, O, Brochet, S, Bruno, G, Caputo, C, Caudron, A, David, P, De Visscher, S, Delaere, C, Delcourt, M, Francois, B, Giammanco, A, Komm, M, Krintiras, G, Lemaitre, V, Magitteri, A, Mertens, A, Musich, M, Piotrzkowski, K, Quertenmont, L, Saggio, A, Vidal Marono, M, Wertz, S, Zobec, J, Alda Junior, W, Alves, F, Alves, G, Brito, L, Correa Martins Junior, M, Hensel, C, Moraes, A, Pol, M, Rebello Teles, P, Belchior Batista Das Chagas, E, Carvalho, W, Chinellato, J, Coelho, E, Da Costa, E, Da Silveira, G, De Jesus Damiao, D, Fonseca De Souza, S, Huertas Guativa, L, Malbouisson, H, Melo De Almeida, M, Mora Herrera, C, Mundim, L, Nogima, H, Sanchez Rosas, L, Santoro, A, Sznajder, A, Thiel, M, Tonelli Manganote, E, Torres Da Silva De Araujo, F, Vilela Pereira, A, Ahuja, S, Bernardes, C, Fernandez Perez Tomei, T, Gregores, E, Mercadante, P, Novaes, S, Padula, S, Romero Abad, D, Ruiz Vargas, J, Aleksandrov, A, Hadjiiska, R, Iaydjiev, P, Misheva, M, Rodozov, M, Shopova, M, Sultanov, G, Dimitrov, A, Litov, L, Pavlov, B, Petkov, P, Fang, W, Gao, X, Yuan, L, Ahmad, M, Bian, J, Chen, G, Chen, H, Chen, M, Chen, Y, Jiang, C, Leggat, D, Liao, H, Liu, Z, Romeo, F, Shaheen, S, Spiezia, A, Tao, J, Wang, C, Wang, Z, Yazgan, E, Zhang, H, Zhang, S, Zhao, J, Ban, Y, Li, J, Li, Q, Liu, S, Mao, Y, Qian, S, Wang, D, Xu, Z, Wang, Y, Avila, C, Cabrera, A, Carrillo Montoya, C, Chaparro Sierra, L, Florez, C, Hernandez, C, Ruiz Alvarez, J, Segura Delgado, M, Courbon, B, Godinovic, N, Lelas, D, Puljak, I, Ribeiro Cipriano, P, Sculac, T, Antunovic, Z, Kovac, M, Brigljevic, V, Ferencek, D, Kadija, K, Mesic, B, Starodumov, A, Susa, T, Ather, M, Attikis, A, Mavromanolakis, G, Mousa, J, Nicolaou, C, Ptochos, F, Razis, P, Rykaczewski, H, Finger, M, Carrera Jarrin, E, El-khateeb, E, Elgammal, S, Mohamed, A, Dewanjee, R, Kadastik, M, Perrini, L, Raidal, M, Tiko, A, Veelken, C, Eerola, P, Kirschenmann, H, Pekkanen, J, Voutilainen, M, Havukainen, J, Heikkila, J, Jarvinen, T, Karimaki, V, Kinnunen, R, Lampen, T, Lassila-Perini, K, Laurila, S, Lehti, S, Linden, T, Luukka, P, Siikonen, H, Tuominen, E, Tuominiemi, J, Tuuva, T, Besancon, M, Couderc, F, Dejardin, M, Denegri, D, Faure, J, Ferri, F, Ganjour, S, Ghosh, S, Gras, P, Hamel de Monchenault, G, Jarry, P, Kucher, I, Leloup, C, Locci, E, Machet, M, Malcles, J, Negro, G, Rander, J, Rosowsky, A, Sahin, M, Titov, M, Abdulsalam, A, Amendola, C, Antropov, I, Baffioni, S, Beaudette, F, Busson, P, Cadamuro, L, Charlot, C, Granier de Cassagnac, R, Jo, M, Lisniak, S, Lobanov, A, Martin Blanco, J, Nguyen, M, Ochando, C, Ortona, G, Paganini, P, Pigard, P, Salerno, R, Sauvan, J, Sirois, Y, Stahl Leiton, A, Strebler, T, Yilmaz, Y, Zabi, A, Zghiche, A, Agram, J, Andrea, J, Bloch, D, Brom, J, Buttignol, M, Chabert, E, Chanon, N, Collard, C, Conte, E, Coubez, X, Fontaine, J, Gele, D, Goerlach, U, Jansova, M, Le Bihan, A, Tonon, N, Van Hove, P, Gadrat, S, Beauceron, S, Bernet, C, Boudoul, G, Chierici, R, Contardo, D, Depasse, P, El Mamouni, H, Fay, J, Finco, L, Gascon, S, Gouzevitch, M, Grenier, G, Ille, B, Lagarde, F, Laktineh, I, Lethuillier, M, Mirabito, L, Pequegnot, A, Perries, S, Popov, A, Sordini, V, Vander Donckt, M, Viret, S, Khvedelidze, A, Lomidze, D, Autermann, C, Feld, L, Kiesel, M, Klein, K, Lipinski, M, Preuten, M, Schomakers, C, Schulz, J, Teroerde, M, Zhukov, V, Albert, A, Dietz-Laursonn, E, Duchardt, D, Endres, M, Erdmann, M, Erdweg, S, Esch, T, Fischer, R, Guth, A, Hamer, M, Hebbeker, T, Heidemann, C, Hoepfner, K, Knutzen, S, Merschmeyer, M, Meyer, A, Millet, P, Mukherjee, S, Pook, T, Radziej, M, Reithler, H, Rieger, M, Scheuch, F, Teyssier, D, Thuer, S, Flugge, G, Kargoll, B, Kress, T, Kunsken, A, Muller, T, Nehrkorn, A, Nowack, A, Pistone, C, Pooth, O, Stahl, A, Aldaya Martin, M, Arndt, T, Asawatangtrakuldee, C, Beernaert, K, Behnke, O, Behrens, U, Bermudez Martinez, A, Bin Anuar, A, Borras, K, Botta, V, Campbell, A, Connor, P, Contreras-Campana, C, Costanza, F, Diez Pardos, C, Eckerlin, G, Eckstein, D, Eichhorn, T, Eren, E, Gallo, E, Garay Garcia, J, Geiser, A, Grados Luyando, J, Grohsjean, A, Gunnellini, P, Guthoff, M, Harb, A, Hauk, J, Hempel, M, Jung, H, Kasemann, M, Keaveney, J, Kleinwort, C, Korol, I, Krucker, D, Lange, W, Lelek, A, Lenz, T, Leonard, J, Lipka, K, Lohmann, W, Mankel, R, Melzer-Pellmann, I, Mittag, G, Mnich, J, Mussgiller, A, Ntomari, E, Pitzl, D, Raspereza, A, Savitskyi, M, Saxena, P, Shevchenko, R, Spannagel, S, Stefaniuk, N, Van Onsem, G, Walsh, R, Wen, Y, Wichmann, K, Wissing, C, Zenaiev, O, Aggleton, R, Bein, S, Blobel, V, Centis Vignali, M, Dreyer, T, Garutti, E, Gonzalez, D, Haller, J, Hinzmann, A, Hoffmann, M, Karavdina, A, Klanner, R, Kogler, R, Kovalchuk, N, Kurz, S, Lapsien, T, Marconi, D, Meyer, M, Niedziela, M, Nowatschin, D, Pantaleo, F, Peiffer, T, Perieanu, A, Scharf, C, Schleper, P, Schmidt, A, Schumann, S, Schwandt, J, Sonneveld, J, Stadie, H, Steinbruck, G, Stober, F, Stover, M, Tholen, H, Troendle, D, Usai, E, Vanhoefer, A, Vormwald, B, Akbiyik, M, Barth, C, Baselga, M, Baur, S, Butz, E, Caspart, R, Chwalek, T, Colombo, F, De Boer, W, Dierlamm, A, Faltermann, N, Freund, B, Friese, R, Giffels, M, Harrendorf, M, Hartmann, F, Heindl, S, Husemann, U, Kassel, F, Kudella, S, Mildner, H, Mozer, M, Plagge, M, Quast, G, Rabbertz, K, Schroder, M, Shvetsov, I, Sieber, G, Simonis, H, Ulrich, R, Wayand, S, Weber, M, Weiler, T, Williamson, S, Wohrmann, C, Wolf, R, Anagnostou, G, Daskalakis, G, Geralis, T, Kyriakis, A, Loukas, D, Topsis-Giotis, I, Karathanasis, G, Kesisoglou, S, Panagiotou, A, Saoulidou, N, Kousouris, K, Evangelou, I, Foudas, C, Gianneios, P, Katsoulis, P, Kokkas, P, Mallios, S, Manthos, N, 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P, Pant, L, Shukla, P, Topkar, A, Aziz, T, Dugad, S, Mahakud, B, Mitra, S, Mohanty, G, Sur, N, Sutar, B, Banerjee, S, Chatterjee, S, Das, P, Guchait, M, Jain, S, Kumar, S, Maity, M, Majumder, G, Mazumdar, K, Sarkar, T, Wickramage, N, Dube, S, Hegde, V, Kapoor, A, Kothekar, K, Pandey, S, Rane, A, Sharma, S, Chenarani, S, Eskandari Tadavani, E, Etesami, S, Khakzad, M, Mohammadi Najafabadi, M, Naseri, M, Paktinat Mehdiabadi, S, Rezaei Hosseinabadi, F, Safarzadeh, B, Zeinali, M, Felcini, M, Grunewald, M, Abbrescia, M, Calabria, C, Colaleo, A, Creanza, D, Cristella, L, De Filippis, N, De Palma, M, Errico, F, Fiore, L, Iaselli, G, Lezki, S, Maggi, G, Maggi, M, Miniello, G, My, S, Nuzzo, S, Pompili, A, Pugliese, G, Radogna, R, Ranieri, A, Selvaggi, G, Sharma, A, Silvestris, L, Venditti, R, Verwilligen, P, Abbiendi, G, Battilana, C, Bonacorsi, D, Borgonovi, L, Braibant-Giacomelli, S, Campanini, R, Capiluppi, P, Castro, A, Cavallo, F, Chhibra, S, Codispoti, G, Cuffiani, M, Dallavalle, G, 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Ahmed, I, Ibrahim, Z, Md Ali, M, Mohamad Idris, F, Wan Abdullah, W, Yusli, M, Zolkapli, Z, Duran-Osuna, M, Castilla-Valdez, H, De La Cruz-Burelo, E, Ramirez-Sanchez, G, Heredia-De La Cruz, I, Rabadan-Trejo, R, Lopez-Fernandez, R, Mejia Guisao, J, Reyes-Almanza, R, Sanchez-Hernandez, A, Carrillo Moreno, S, Oropeza Barrera, C, Vazquez Valencia, F, Eysermans, J, Pedraza, I, Salazar Ibarguen, H, Uribe Estrada, C, Morelos Pineda, A, Krofcheck, D, Butler, P, Ahmad, A, Hassan, Q, Hoorani, H, Saddique, A, Shah, M, Shoaib, M, Waqas, M, Bialkowska, H, Bluj, M, Boimska, B, Frueboes, T, Gorski, M, Kazana, M, Nawrocki, K, Szleper, M, Zalewski, P, Bunkowski, K, Byszuk, A, Doroba, K, Kalinowski, A, Konecki, M, Krolikowski, J, Misiura, M, Olszewski, M, Pyskir, A, Walczak, M, Bargassa, P, Beirao Da Cruz E Silva, C, Di Francesco, A, Faccioli, P, Galinhas, B, Gallinaro, M, Hollar, J, Leonardo, N, Lloret Iglesias, L, Nemallapudi, M, Seixas, J, Strong, G, Toldaiev, O, Vadruccio, D, Varela, J, Alexakhin, V, 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Karchin, P.E., Poudyal, N., Sturdy, J., Thapa, P., Zaleski, S., Brodski, M., Buchanan, J., Caillol, C., Dasu, S., Dodd, L., Duric, S., Gomber, B., Grothe, M., Herndon, M., Hervé, A., Hussain, U., Klabbers, P., Lanaro, A., Levine, A., Long, K., Loveless, R., Ruggles, T., Savin, A., Smith, N., Smith, W.H., Taylor, D., Woods, N., and Çukurova Üniversitesi, Fen-Edebiyat Fakültesi, Fizik Bölümü
Subjects: 13000 GeV-cms, Beyond Standard Model, Hadron-Hadron scattering (experiments), Particle and resonance production, ATLAS DETECTOR, 7. Clean energy, 01 natural sciences, Physics, Particles & Fields, Hadron-Hadron scattering (experiments), scattering [p p], Nuclear Experiment, Z0: hadronic decay, Beyond Standard Model, Particle, and resonance production, PP COLLISIONS, HIGGS-BOSON, P(P)OVER-BAR COLLISIONS, PARTICLE, LHC, PHOTON, DECAYS, MASS, Large Hadron Collider, Particle and resonance production, Z0: decay modes, Physics, 3. Good health, channel cross section: branching ratio: upper limit, muon: pair production, CERN LHC Coll, final state: hadronic, Physical Sciences, Physique des particules élémentaires, Higgs boson, PARTICLE PHYSICS, colliding beams [p p], Mass energy, p p: scattering, production [resonance], 114 Physical sciences, ddc:530, pair production [electron], 010306 general physics, S055H2O, 01 Mathematical Sciences, Science & Technology, Muon, 010308 nuclear & particles physics, Branching fraction, LARGE HADRON COLLIDER, CMS, decay modes [Z0], Resonance production, p p: colliding beams, Physics::Instrumentation and Detectors, Physics beyond the Standard Model, Hadron, bottom: particle identification, Jet (particle physics), High Energy Physics - Experiment, electron: pair production, Z bosons, resonance: mass: lower limit, [PHYS.HEXP]Physics [physics]/High Energy Physics - Experiment [hep-ex], Particle production, 02 Physical Sciences, resonance: radiative decay, hadronic decay [Z0], radiative decay [resonance], photon, Settore FIS/01 - Fisica Sperimentale, Nuclear & Particles Physics, Phonons, particle identification [bottom], Nuclear and High Energy Physics, narrow resonance, Particle Physics - Experiment, Particle physics, data analysis method, Bottom quark, hadronic [final state], CMS collaboration, proton-proton collisions, BSM, Z boson, mass: lower limit [resonance], 0103 physical sciences, pair production [muon], structure, branching ratio: upper limit [channel cross section], hep-ex, High Energy Physics::Phenomenology, high energy physics, experimental particle physics, standard model, leptonic decay [Z0], Z0: leptonic decay, Physics::Accelerator Physics, High Energy Physics::Experiment, resonance: production, experimental results
Abstract: A search is presented for resonances decaying to a Z boson and a photon. The analysis is based on data from proton-proton collisions at a center-of-mass energy of 13 TeV, corresponding to an integrated luminosity of 35.9 fb[superscript −1], and collected with the CMS detector at the LHC in 2016. Two decay modes of the Z boson are investigated. In the leptonic channels, the Z boson candidates are reconstructed using electron or muon pairs. In the hadronic channels, they are identified using a large-radius jet, containing either light-quark or b quark decay products of the Z boson, via jet substructure and advanced b quark tagging techniques. The results from these channels are combined and interpreted in terms of upper limits on the product of the production cross section and the branching fraction to Zγ for narrow and broad spin-0 resonances with masses between 0.35 and 4.0 TeV, providing thereby the most stringent limits on such resonances. Keywords: Beyond Standard Model, Hadron-Hadron scattering (experiments), Particle and resonance production, National Science Foundation (U.S.), United States. Department of Energy
Published: 2018
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41. PHOTOPHYSICAL BEHAVIOR OF COUMARIN DERIVATIVES AND THEIR INHIBITORY EFFECT ON AChE ACTIVITY

Author: Prayasee Baruah and Sivaprasad Mitra
Published: 2018
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42. Intramolecular charge transfer in coumarin based donor-acceptor systems: Formation of a new product through planar intermediate

Author: Smritakshi Phukan, Amarta Kumar Pal, Achikanath C. Bhasikuttan, Mithu Saha, and Sivaprasad Mitra
Subjects: Chemistry, Hydrogen bond, General Chemical Engineering, Imine, General Physics and Astronomy, General Chemistry, Photochemistry, Fluorescence spectroscopy, chemistry.chemical_compound, Intramolecular force, Excited state, Density functional theory, Steady state (chemistry), Ground state
Abstract: Fluorescence behavior and intramolecular charge transfer (ICT) property of N,N′-dimethylamino substituted anil derivative of coumarinyl amine was studied by steady state and time-resolved fluorescence spectroscopy in combination with density functional theory calculation. Quantitative analysis of the effect of solvent hydrogen bonding on several spectral parameters was done using multiple regression analysis based on Kamlet–Taft model. The present system shows an additional long wavelength fluorescence band almost instantaneously in presence of methanol in sharp contrast to the model unsubstituted analogue. This new fluorescence band is believed to be due to the formation of a new isomer (cis-type) through a planar intermediate. While there is a substantial barrier (∼50 kJ mol−1) in the ground state, the isomerization process in the excited state in polar-protic environment proceeds very fast and believed to be catalyzed by hydrogen bond formation at the imine nitrogen atom in combination with stabilization of the resulting species through ICT.
Published: 2015
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43. Correlation of cholinergic drug induced quenching of acetylcholinesterase bound thioflavin-T fluorescence with their inhibition activity

Author: Atanu Bhattacharjee, Sivaprasad Mitra, Mostofa Ataur Rohman, Arun Bahadur Gurung, Mullah Muhaiminul Islam, and Kripamoy Aguan
Subjects: 0301 basic medicine, 030103 biophysics, Fluorophore, Fluorescence, Analytical Chemistry, 03 medical and health sciences, chemistry.chemical_compound, 0302 clinical medicine, Benzothiazoles, Instrumentation, Spectroscopy, biology, Hydrolysis, Active site, Hydrogen Bonding, Acetylcholinesterase, Atomic and Molecular Physics, and Optics, Molecular Docking Simulation, Kinetics, Thiazoles, Spectrometry, Fluorescence, chemistry, Biochemistry, Docking (molecular), biology.protein, Thermodynamics, Thioflavin, Cholinesterase Inhibitors, 030217 neurology & neurosurgery, Fluorescence anisotropy, Plate reader
Abstract: The development of new acetylcholinesterase inhibitors (AChEIs) and subsequent assay of their inhibition efficiency is considered to be a key step for AD treatment. The fluorescence intensity of thioflavin-T (ThT) bound in the active site of acetylcholinesterase (AChE) quenches substantially in presence of standard AChEI drugs due to the dynamic replacement of the fluorophore from the AChE active site as confirmed from steady state emission as well as time-resolved fluorescence anisotropy measurement and molecular dynamics simulation in conjunction with docking calculation. The parametrized % quenching data for individual system shows excellent correlation with enzyme inhibition activity measured independently by standard Ellman AChE assay method in a high throughput plate reader system. The results are encouraging towards design of a fluorescence intensity based AChE inhibition assay method and may provide a better toolset to rapidly evaluate as well as develop newer AChE-inhibitors for AD treatment.
Published: 2017

44. Photophysical properties and excited state intramolecular proton transfer in 2-hydroxy-5-[(E)-(4-methoxyphenyl)diazenyl]benzoic acid in homogeneous solvents and micro-heterogeneous environments

Author: Pynsakhiat Miki Gashnga, Tushar S. Basu Baul, T. Sanjoy Singh, and Sivaprasad Mitra
Subjects: Hydrogen bond, Biophysics, General Chemistry, Condensed Matter Physics, Photochemistry, Biochemistry, Binding constant, Micelle, Fluorescence, Atomic and Molecular Physics, and Optics, Fluorescence spectroscopy, chemistry.chemical_compound, chemistry, Intramolecular force, Critical micelle concentration, Benzoic acid
Abstract: A systematic study on the photophysical properties and excited state intramolecular proton transfer (ESIPT) behavior of 2-hydroxy-5-[( E )-(4-methoxyphenyl)diazenyl]benzoic acid, is reported using steady-state and time-resolved fluorescence spectroscopy in homogeneous solvents as well as in different micro-heterogeneous environments. Depending on the nature of intramolecular hydrogen bond (IHB), the salicylic acid derivative may exist in two different ground state conformers ( I and II ). Structure I having IHB between the carbonyl oxygen and phenolic hydrogen can undergo ESIPT upon excitation as evidenced by largely Stokes-shifted fluorescence at ~455 nm; whereas, normal fluorescence in the blue side of the spectrum (~410 nm) is due to the spontaneous emission from conformer II . The results in homogeneous solvents were compared with those in bio-mimicking environments of β-cyclodextrin (CD) and surfactants. The intensity of the ESIPT fluorescence increases substantially upon encapsulation of the probe into the cyclodextrin as well as micellar nano-cavities. Detailed analysis of the spectroscopic data indicates that the probe forms 1:1 complex with CD in aqueous medium. Binding constant of the probe with the micelles as well as critical micelle concentration was obtained from the variation of fluorescence intensity on increasing concentration of different surfactants in aqueous medium.
Published: 2014
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45. Deciphering the interactions of substituted chromones possessing acetylcholinesterase inhibition activity in human serum albumin matrix

Author: Prayasee Baruah, Anindita Bhatta, Sivaprasad Mitra, and Mostofa Ataur Rohman
Subjects: Circular dichroism, Quenching (fluorescence), Stereochemistry, 02 engineering and technology, Plasma protein binding, 010402 general chemistry, 021001 nanoscience & nanotechnology, Condensed Matter Physics, Human serum albumin, 01 natural sciences, Acetylcholinesterase, Fluorescence, Atomic and Molecular Physics, and Optics, 0104 chemical sciences, Electronic, Optical and Magnetic Materials, chemistry.chemical_compound, chemistry, Chromone, Materials Chemistry, medicine, Titration, Physical and Theoretical Chemistry, 0210 nano-technology, Spectroscopy, medicine.drug
Abstract: A combination of different biophysical techniques is applied in conjunction with molecular docking calculation to explore the binding interaction of two substituted chromone derivatives namely 7-amino-2-methylchromone (AMC) and 3-cyanochromone (CyC), both of which are screened as potential acetylcholinesterase inhibitors, with human serum albumin (HSA). Analysis of intrinsic tryptophan fluorescence quenching reveals the Stern-Volmer constant (KSV) for CyC (~1.2 × 105 M−1) to be one order in magnitude higher than AMC (~3.9 × 104 M−1). Analysis of fluorescence lifetime data indicates static quenching mechanism for AMC; while a significant contribution from the dynamic (collisional) quenching also exits for CyC. The difference in binding thermodynamics of the chromones into the protein binding domain is mainly due to the difference in the primary forces responsible for the binding. The fluorescence titration results are in nice agreement with the complementary circular dichroism (CD) experiments as well as with the results from molecular docking calculation. The results indicate that while CyC binds to Domain IIA (Sudlow's site 1) of HSA with a greater binding affinity of −28.84 kJ/mol, AMC binds at an alternate position, site IB with a lower binding affinity (−27.19 kJ/mol).
Published: 2019
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46. Studies on the inclusion complexation between intramolecular charge transfer probe trans-ethyl p-(dimethylamino) cinamate and β-cyclodextrin in presence of ionic and nonionic surfactants

Author: T. Sanjoy Singh and Sivaprasad Mitra
Subjects: chemistry.chemical_classification, Cyclodextrin, Biophysics, Analytical chemistry, Ionic bonding, General Chemistry, Condensed Matter Physics, Photochemistry, Biochemistry, Binding constant, Fluorescence, Atomic and Molecular Physics, and Optics, Fluorescence spectroscopy, Hydrophobic effect, chemistry, Critical micelle concentration, Intramolecular force
Abstract: The intramolecular charge transfer (ICT) fluorescence of trans -ethyl p -(dimethylamino) cinamate (EDAC) is used to monitor the complexation behavior of this probe with surfactants/β-CD by steady state and picosecond time-resolved fluorescence spectroscopy. The ICT fluorescence band intensity was found to increase with concomitant blue shift in presence of surfactants/β-CD. The encapsulation behavior was further characterized by increase in emission yield as well as lifetime values. Detailed analyses of the spectroscopic data indicate that the probe forms 1:1 complex with β-CD in aqueous medium. However, in presence of surfactants, 1:1 complex is formed below the critical micelle concentration (cmc) value; whereas, 1:2 complexes are formed under fully micellized condition.
Published: 2013
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47. Specific solvent effect on lumazine photophysics: A combined fluorescence and intrinsic reaction coordinate analysis

Author: N. Shaemningwar Moyon, Smritakshi Phukan, Pynsakhiat Miki Gashnga, and Sivaprasad Mitra
Subjects: Hydrogen, Chemistry, Hydrogen bond, Excited state, Solvatochromism, General Physics and Astronomy, chemistry.chemical_element, Density functional theory, Physical and Theoretical Chemistry, Solvent effects, Photochemistry, Tautomer, Fluorescence spectroscopy
Abstract: The photophysical properties and tautomerization behavior of neutral lumazine were studied by fluorescence spectroscopy and density functional theory calculation. A quantitative estimation of the contributions from different solvatochromic parameters, like solvent polarizibility ( π ∗ ), hydrogen bond donation ( α ) and hydrogen bond accepting ( β ) ability of the solvent, was made using linear free energy relationships based on the Kamlet–Taft equation. The analysis reveals that the hydrogen bond acceptance ability of the solvent is the most important parameter characterizing the excited state behavior of lumazine. Theoretical calculations result predict an extensive charge redistribution of lumazine upon excitation corresponding to the N3 and N1 proton dissociation sites by solvents in the ground and excited states, respectively. Comparison of S 0 and S 1 state potential energy curves constructed for several water mediated tautomerization processes by intrinsic reaction coordinate analysis of lumazine-H 2 O cluster shows that (3,2) and (1,8) hydrogen migrations are the most favorable processes upon excitation.
Published: 2013
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48. Synthesis and fluorescence behavior of photoactive polyhydroquinoline derivatives: A combined experimental and DFT study

Author: Smritakshi Phukan, Mithu Saha, Sivaprasad Mitra, and Amarta Kumar Pal
Subjects: Chemistry, Organic Chemistry, Time-dependent density functional theory, Electron, Photochemistry, Fluorescence, Analytical Chemistry, Inorganic Chemistry, symbols.namesake, Intramolecular force, Stokes shift, Nitro, symbols, Steady state (chemistry), Time-resolved spectroscopy, Spectroscopy
Abstract: A series of biologically important substituted polyhydroquinoline derivatives were synthesized by one-pot protocol using palladium nanoparticles as an efficient catalyst. Photophysical behavior of the synthesized systems was monitored using steady state and time-resolved fluorescence techniques in a series of neat and mixed solvents as well as by time dependent density functional theory (TDDFT). An additional large Stokes-shifted fluorescence band is observed in N,N′-dimethylamino derivative over the nitro and/or methoxy substituted system and is believed to be originated due to the formation of an intramolecular charge transfer (ICT) state. The intensity of this additional fluorescence band decreases considerably in polar protic environment and also in presence of trace amount of acid, confirming the involvement of nitrogen lone-pair of electrons towards the formation of the charge transfer state.
Published: 2013
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49. Fluorescence spectroscopic studies on substituted porphyrins in homogeneous solvents and cationic micellar medium

Author: Dalip Kumar, Smritakshi Phukan, Anil Kumar, Bhupendra Mishra, Sivaprasad Mitra, and K. P. Chandra Shekar
Subjects: Biophysics, Cationic polymerization, Substituent, Protonation, General Chemistry, Condensed Matter Physics, Photochemistry, Biochemistry, Fluorescence, Porphyrin, Acceptor, Atomic and Molecular Physics, and Optics, Photoinduced electron transfer, chemistry.chemical_compound, chemistry, Polar effect
Abstract: Steady state and time-resolved fluorescence properties of porphyrin appended 1,3,4-oxadiazoles and thiazoles were described in homogeneous medium as well as in presence of cationic surfactant cetyltrimethylammonium bromide (CTAB). The electron withdrawing substituent on the porphyrin moiety in both the cases make a donor–spacer–acceptor type of intramolecular photoinduced electron transfer (PET) system resulting substantial quenching in porphyrin fluorescence due to partial energy migration towards the acceptor in the excited state. The increase in fluorescence yield as well as appreciable difference in fluorescence decay behavior in aqueous buffer solution of pH 4.2 from that in chloroform solution is believed due to partial protonation of the porphyrin ring. All the investigated systems show preferential binding into the interfacial region of the micellar sub-domain with varying degree of penetration depending on the nature of the substituent. Almost 2–4 fold increase in fluorescence yield for the probes is explained on the basis of restricted flexibility and corresponding decrease in total nonradiative rate inside the micellar interface layer.
Published: 2013
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50. Facile Synthesis, Characterization, and Fluorescence Studies of Novel Porphyrin Appended Thiazoles

Author: K. P. Chandra Shekar, Anil Kumar, Sivaprasad Mitra, Bhupendra Mishra, Dalip Kumar, and Smritakshi Phukan
Subjects: chemistry.chemical_compound, Chloroform, chemistry, Excited state, Organic Chemistry, Moiety, Ring (chemistry), Photochemistry, Thiazole, Combinatorial chemistry, Porphyrin, Fluorescence, High yielding
Abstract: A facile and high yielding synthesis of porphyrin appended thiazoles 5 from the reaction of 5-(4-thiocarboxamidophenyl)-10,15,20-triphenylporphyrin with α-bromo ketones has been described. The fluorescence studies of synthesized porphyrin appended thiazoles 5 in chloroform indicate that porphyrin π system is not greatly perturbed by substitution of a thiazole moiety at meso-phenyl ring even in the excited state.
Published: 2013
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