72 results on '"B, Vinay Kumar"'
Search Results
52. Antibacterial, Molecular Docking, DNA Binding and Photocleavage Studies on Novel Heterocyclic Pyrazoles
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Halehatty S. Bhojya Naik, B. Vinay Kumar, N. Sharath, and Joy Hoskeri
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chemistry.chemical_compound ,DNA Intercalation ,chemistry ,DNA damage ,Stereochemistry ,Docking (molecular) ,In silico ,Intercalation (chemistry) ,General Medicine ,Pyrazole ,Antibacterial activity ,DNA - Abstract
The antibacterial activity, in-silico DNA molecular docking, DNA binding and photo cleavage studies of newly synthesized pyrazole is described. Antibacterial potential of these compounds screened against a wide range of Gram-positive and Gram-negative bacteria showed significant zone of inhibition and MIC with standard drug ciproflaxin is investigated. Among all the orientation of binding, fourth orientation showed significant binding and revealed that the binding and docking energy of 4a was -8.62 and -8.66 and inhibition constant 7.46 X e -6 . The absorption spectra showed the dynamic interaction with CT DNA and as proficient DNA intercalator (Kb = 4.5×10 4 M -1 ). The viscosity measurements and thermal denaturation affords the positive results towards DNA intercalation in both the studies. The light induced DNA damage was pragmatic in the absence of various ‘‘inhibitors’’ shows in photo cleavage activities at 360 nm.
- Published
- 2011
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53. Synthesis of Functionalized Iron Oxide Nanoparticle with Amino Pyridine Moiety and Studies on Their Catalytic Behavior
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Halehatty S. Bhojya Naik, D. Girija, B. Vinay Kumar, and C.N. Sudhamani
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Green chemistry ,Materials science ,Inorganic chemistry ,General Engineering ,Iron oxide ,Energy Engineering and Power Technology ,Nanoparticle ,Catalysis ,chemistry.chemical_compound ,chemistry ,Pyridine ,Surface modification ,Reactivity (chemistry) ,Iron oxide nanoparticles ,Nuclear chemistry - Abstract
Aim: The main objective of this paper is to study the synthesis of functionalized iron oxide nanoparticle and its reactivity towards chromene synthesis Study design: Functionalized iron oxide nanoparticle study. Place and duration of study: Department of Studies and Research in Industrial Chemistry, School of Chemical Sciences, Kuvempu University, Shankaraghatta, between December 2009 and July 2010. Methodology: This paper describes synthesis of stable functionalized iron oxide nanoparticles through surface modification of magnetic iron oxide nanoparticles by amino pyridine. Iron oxide nanoparticles were synthesized by co-precipitation method and the surface modification process was achieved by treating the nanoparticles with (chloro propyl trimethoxy silane) CPTS and aminopyridine. The developed functionalized iron oxide nanoparticle was evaluated as the catalyst for synthesis of chromones under MW irradiation conditions. Results: The catalysts were magnetically recovered and reusable without significant loss of their catalytic efficiency. To receive morphological and structural information on the obtained functionalized nanoparticle, the samples were analyzed by X-ray diffraction (XRD) measurements, FTIR and scanning electron microscopy (SEM) imaging. All synthesized chromene derivatives were characterized using analytical techniques such as IR, H NMR, and mass spectroscopy. Also the identity of these compounds was easily established by comparison of their melting point with those of reported samples. Conclusion: In summary, we have developed a new magnetically recyclable and Research Article American Chemical Science Journal, 1(3): 97-108, 2011 98 efficient functionalized magnetic nano catalyst for the chromene synthesis. Magnetic nanoparticle catalyst achieves a simple separation of catalyst without filtration including high yield in product.
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- 2011
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54. Benzo[h]quinoline based Macrocyclic Copper(II), Cobalt(II) Complexes: Synthesis, Characterization and Light induced DNA Cleavage Studies
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H. S. Bhojya Naik, B. Vinay Kumar, N. Sharath, D. S. Lamani, B. Vijaya Kumar, T. Aravinda, M. Yogesh, H. R. Prakash Naik, and P.N. Prashanth Kumar
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Polymers and Plastics ,Chemistry ,Ligand ,Stereochemistry ,Quinoline ,chemistry.chemical_element ,General Chemistry ,Copper ,Metal ,chemistry.chemical_compound ,Transition metal ,visual_art ,Polymer chemistry ,Materials Chemistry ,Ceramics and Composites ,visual_art.visual_art_medium ,Molecule ,Macrocyclic ligand ,Cobalt - Abstract
A new ligand dibenzo[h]quinolineno[1,3,7,9] tetraazacyclododecine-7,15 (14H, 16H)-dibenzene (L) and its Co(II)/Cu(II) metal complexes of type [MLX2] (Where (M = Co(II) (5), Cu(II) (6) and X = Cl) were synthesized and are well characterized by FT-IR, 1H-NMR, FAB mass elemental analysis, and electronic spectral data. The role of the cobalt/copper metals in photo-induced DNA cleavage reactions was explored by designing complex molecules having macrocyclic structure. Finally, we have shown that photocleavage of plasmid DNA is more efficiently enhanced when this macrocyclic ligand is irradiated in the presence of copper(II) than that of cobalt metal.
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- 2009
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55. Photocatalytic Degradation of Congo Red Dye Using Silver Doped TiO2 Nanosheets
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B. Vinay Kumar, P. E. JagadeeshBabu, and Abhinav K. Nair
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Anatase ,Materials science ,Doping ,02 engineering and technology ,010402 general chemistry ,021001 nanoscience & nanotechnology ,01 natural sciences ,Titanate ,0104 chemical sciences ,Congo red ,chemistry.chemical_compound ,Hydrofluoric acid ,chemistry ,Transmission electron microscopy ,Photocatalysis ,Degradation (geology) ,0210 nano-technology ,Nuclear chemistry - Abstract
TiO2 nanosheets were synthesized from tetrabutyl titanate precursor via solvothermal treatment using Hydrofluoric acid as structure directing agent. Anatase phase nanosheets could be obtained by this method, imparting good photocatalytic activity. In order to enhance photocatalytic activity, silver doping of TiO2 nanosheets was done using photo-deposition method under ultra-violet light irradiation. These nanosheets were characterized using Transmission electron microscopy, X-ray diffraction and Energy-dispersive X-ray spectroscopy. Photocatalytic activity was estimated by means of congo red dye degradation studies under ultra-violet light irradiation. The silver doped TiO2 nanosheets showed enhanced photocatalytic activity.
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- 2016
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56. Radio resource allocation with energy efficiency-throughput balancing for LTE downlink
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B. Malarkodi, B Vinay Kumar, and B. Rebekka
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Engineering ,business.industry ,Quality of service ,Telecommunications link ,Resource management ,Algorithm design ,Throughput ,Energy consumption ,business ,Energy (signal processing) ,Efficient energy use ,Computer network - Abstract
Energy consumption in wireless communication systems is increasing tremendously, wherein most of the energy consumedis by the evolved NodeBs in LTE network. Nowadays the research trend is majorly focused on Green communication which aims at reducing the Energy consumed in a network. In this paper, a radio resource allocation algorithm that is meant to balance energy efficiency and throughput maximization is proposed. The proposed algorithm is used to allocate Resource Blocks (RBs) to users considering the data rate requirements of the users based on priority for LTE downlink while maintaining Quality of Service (QoS). In this way the scarce spectrum is effectively utilized and the energy efficiency (EE) is improved. The proposed algorithm is compared with conventional scheduling algorithms such as Round Robin (RR), Best CQI (Best CQI/BCQI) and is analyzed on the basis of throughput, fairness and Energy Consumption Ratio (ECR).
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- 2015
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57. DNA binding, photoactivated DNA cleavage and cytotoxic activity of Cu(II) and Co(II) based Schiff-base azo photosensitizers
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Atanu Barik, K. Indira Priyadarsini, H. S. Bhojya Naik, B. Vinay Kumar, S.M. Pradeepa, and M. C. Prabhakara
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Spectrophotometry, Infrared ,Stereochemistry ,Carboxylic acid ,Proton Magnetic Resonance Spectroscopy ,Quantum yield ,Electrons ,Nucleic Acid Denaturation ,Mass Spectrometry ,Analytical Chemistry ,chemistry.chemical_compound ,Inhibitory Concentration 50 ,Animals ,Humans ,Photosensitizer ,DNA Cleavage ,Instrumentation ,Spectroscopy ,Schiff Bases ,Benzoic acid ,chemistry.chemical_classification ,Electrophoresis, Agar Gel ,Schiff base ,Photosensitizing Agents ,Singlet Oxygen ,Ligand ,Viscosity ,Cobalt ,DNA ,Atomic and Molecular Physics, and Optics ,chemistry ,Solubility ,MCF-7 Cells ,Cattle ,Spectrophotometry, Ultraviolet ,pUC19 ,Copper - Abstract
A new class of Cu(II) and Co(II) complexes of azo-containing Schiff base of the type [Cu(L1)2] and [Co(L1)2], where L1 = 4-[(E)-{2-hydroxy-3-[(E)-(4-bromophenyl)diazenyl]benzylidene}amino]benzoic acid have been synthesized and characterized. Extension of conjugation and the presence of free carboxylic acid group of the ligand L1 increased the wavelength of the complexes from visible region to the near IR region (620–850 nm). The Cu(II) and Co(II) complexes interacted with CT-DNA via intercalative mode with the respective Kb value of 3.2 × 104 M−1 and 2.9 × 104 M−1 and acted as proficient photocleavers of SC pUC19 DNA in UV-A light, forming 1O2 as the reactive oxygen species with the quantum yield of 0.38 and 0.36, respectively. Furthermore, the Cu(II) and Co(II) complexes showed photocytotoxicity toward two selected tumor cell lines MCF-7 and A549 by 3-(4,5-Dimethylthiazol-2-yl)-2,5-diphenyltetrazoliumbromide (MTT) method, and the Cu(II) complex exhibits higher photocytotoxicity than Co(II) complex against each of the selected cell lines, this result is identical with their DNA binding ability order.
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- 2014
58. ChemInform Abstract: New Green, Recyclable Magnetic Nanoparticles Supported Amino Acids as Simple Heterogenous Catalysts for Knoevenagel Condensation
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H. S. Bhojya Naik, D. Girija, B. Vinay Kumar, C.N. Sudhamani, and K. N. Harish
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inorganic chemicals ,Green chemistry ,chemistry.chemical_classification ,Chemistry ,Iron oxide ,General Medicine ,Coumarin ,Condensation reaction ,Catalysis ,Amino acid ,chemistry.chemical_compound ,Magnetic nanoparticles ,Organic chemistry ,heterocyclic compounds ,Knoevenagel condensation - Abstract
Iron oxide supported amino acid as recoverable catalyst is applied in Knoevenagel condensation leading to different substituted coumarin derivatives.
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- 2013
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59. Synthesis, DNA binding, and photonuclease activity of new tetraaza macrocyclic constrained isoxazole rings as subunit in metal complexes
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B. Vinay Kumar, N. Sharath, and H. S. Bhojya Naik
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Macrocyclic Compounds ,Stereochemistry ,Base pair ,Intercalation (chemistry) ,Ligands ,Biochemistry ,Metal ,chemistry.chemical_compound ,Structure-Activity Relationship ,Octahedral molecular geometry ,Genetics ,Organometallic Compounds ,Molecule ,Animals ,Isoxazole ,Aza Compounds ,Binding Sites ,Photosensitizing Agents ,Dose-Response Relationship, Drug ,Molecular Structure ,Chemistry ,Ligand ,Viscosity ,Temperature ,General Medicine ,DNA ,Isoxazoles ,Binding constant ,Oxygen ,Crystallography ,visual_art ,visual_art.visual_art_medium ,Molecular Medicine ,Cattle - Abstract
The DNA-binding and photonuclease activity of newly synthesized tetra-azamacrocyclic ligand L (C(32)H(32)N(8)O(4)) and its complexes of type [MLCl(2)] and [ML]Cl(2) (where M = Co(II), Fe(II) and Cu(II); L = N,N'-[3-(4-{5-[(2-amino-ethylamino)-methyl]-isoxazol-3yl}-phenyl)-isoxazol-5-yl methyl-ethane-1,2-diamine] are specified. An octahedral geometry has been proposed for Fe(II) and Co(II) complexes, while the Cu(II) complex has a square planar environment. The absorption spectral results indicate that the complexes bind with the base pairs of DNA, with an intrinsic binding constant K(b) of Fe(II), Co(II), and Cu(II) complexes found to be 3.2 × 10(4) M(-1), 5.3 × 10(4) M(-1), and 4.2 × 10(4) M(-1), respectively, in 5 mM Tris-HCl/50 mM NaCl buffer at pH 7.2. The large enhancement in the relative viscosity of DNA on binding to the complexes supports the proposed DNA binding modes. The viscosity and thermal denaturation studies sustain the effective intercalation with DNA. The DNA photocleavage studies demonstrated that compounds exhibit significant photonuclease activity by a concentration dependent on singlet oxygen mediated mechanism.
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- 2012
60. ChemInform Abstract: ZnO Nanoparticle as Catalyst for Efficient Green One-Pot Synthesis of Coumarins Through Knoevenagel Condensation
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B. Vinay Kumar, Halehatty S. Bhojya Naik, B. Vijaya Kumar, and D. Girija
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Green chemistry ,Chemical engineering ,chemistry ,One-pot synthesis ,chemistry.chemical_element ,Nanoparticle ,Knoevenagel condensation ,General Medicine ,Zinc ,Microwave ,Reusability ,Catalysis - Abstract
Green chemistry protocols with the reusability of the nano particle as catalyst in the synthesis of coumarins is described. The zinc oxide (ZnO) nanoparticles functions as highly effective catalyst for the reactions of various o-hydroxy benzaldehydes with 1,3-dicarbonyl compounds under microwave and thermal conditions to afford the corresponding coumarins in moderate to good yields. The catalyst is inexpensive, stable, can be easily recycled and reused for several cycles with consistent activity.
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- 2011
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61. Synthesis and biological evaluation of new Tetra-aza macrocyclic scaffold constrained oxadiazole, thiadiazole and triazole rings
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H. V. Sudeep, B. Vinay Kumar, N. Sharath, H. S. Bhojya Naik, D. Girija, and H. Joy Hoskeri
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DNA Replication ,Oxadiazoles ,Macrocyclic Compounds ,Bacteria ,Stereochemistry ,Triazole ,DNA replication ,Pharmaceutical Science ,Oxadiazole ,DNA ,Microbial Sensitivity Tests ,Triazoles ,Antioxidants ,Anti-Bacterial Agents ,chemistry.chemical_compound ,Structure-Activity Relationship ,chemistry ,Sulfanyl ,Ciprofloxacin ,Drug Discovery ,Thiadiazoles ,Molecule ,Antibacterial activity ,Acetamide - Abstract
A new series of N,N'-(benzene-1,3-diyldi-1,3,4-oxadiazole-5,2-diyl)bis{2-[(5-benzene-1,3-diyl-1,3,4-oxadiazol-2-yl)amino]acetamide}(macrocycle 1), N,N'-(benzene-1,3-diyldi-1,3,4-thiadiazole-5,2-diyl)bis{2-[(5-benzene-1,3-diyl-1,3,4-thiadiazol-2-yl)amino]acetamide} (macrocycle 2) and S,S'-[benzene-1,3-diylbis(4H-1,2,4-triazole-5,3-diyl)]bis{[(5-benzene-1,3-diyl-4H-1,2,4-triazol-3-yl)sulfanyl]ethanethioate}(macrocycle 3) was synthesized from isophthalic dihydrazide (4) through a multistep reaction sequence. All the synthesized compounds were screened for their inhibitory effect against four different bacterial strains: P. aeruginosa ATCC-20852, K. pneumoniae MTCC-618, S. aureus ATCC- 29737, S. typhi MTCC- 3214. The synthesized compounds showed a significant zone of inhibition and the results were comparable with that of the standard drug ciprofloxacin. The synthesized compounds were further studied for their possible in vitro antioxidant effects by DPPH scavenging, total antioxidant capacity, total reductive capacity and H(2) O(2) scavenging activity. The results indicated that the in vitro antioxidant activity for all the three molecules was efficient when compared to the standards. The DNA interaction behavior of macrocycles 1-3 with CT-DNA was investigated by the absorption spectra obtained (K(b) constant for 1 is 4.53 × 10(4) M(-1) , for 2 is 5.75 × 10(4) M(-1) and for 3 is 5.86 × 10(4) M(-1) ). Based on the results it can be interpreted that the reducing power effect of the newly synthesized compounds demonstrates a direct effect on DNA binding and hence inhibiting the bacterial growth through their action on DNA by inhibiting DNA replication or DNA transcription.
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- 2011
62. A Rapid RP HPLC Method Development and Validation for the Analysis of Divalproex in Bulk and Pharmaceutical Dosage Forms
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Shiny Ganji, D. Samson Israel, and B. Vinay Kumar
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Detection limit ,Divalproex ,Active ingredient ,Analyte ,Chromatography ,Calibration curve ,Linearity ,Dosage form ,Mathematics ,Volumetric flow rate ,Biomedical engineering - Abstract
The prime aim of the current work is to develop and validate a novel, specific, sensitive, precise, rapid and faster isocratic elution, RP HPLC method for estimation of Divalproex in bulk and pharmaceutical dosage forms. Chromatographic separation was achieved on Agilent SB C18, (50 x 4.6 mm, 5μ) using an isocratic mode with mobile phase composed of Buffer and Acetonotrile are taken in 60: 40%v/v(PH 4) The flow rate was 1.0ml/min, temperature is maintained at 30°C and detection was made at 210 nm. The run time was 8 min. The developed method was validated according to the ICH guide lines and different analytical parameters such as linearity, precision, accuracy, specificity, limit of detection, limit of quantitation were determined. The linearity of calibration curve for each analyte is in concentration range of 25-150ppm. There exists good correlation between peak area and analyte concentration. Relative standard deviation values for Divaprolex is 1.24. LOD for drug is 2.3 and LOQ is 9.4. Hence the proposed method is highly sensitive, precise, accurate, robust and fast. The short retention time allows the analysis of large number of samples in short period of time and it is cost effective, so it can be successfully applied for routine analysis of active pharmaceutical ingredient and related impurities in bulk and pharmaceutical dosage forms.
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- 2016
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63. A New Fast Architecture for HD H.264 CAVLC Multi-syntax Decoder and its FPGA Implementation
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D.R. Sai Sharan and B. Vinay Kumar
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ComputingMethodologies_PATTERNRECOGNITION ,Computer science ,business.industry ,Feature extraction ,Gabor wavelet ,ComputingMethodologies_IMAGEPROCESSINGANDCOMPUTERVISION ,Pattern recognition ,Computer vision ,Artificial intelligence ,business ,Facial recognition system ,Classifier (UML) - Abstract
This paper introduces Gabor wavelet grids localized within the region of importance (ROI) for a robust pattern recognition system that is capable of recognizing various image classes. The representation of the patterns is based on Gabor wavelet transforms. The features are extracted as a vector of values using an optimally chosen multiple frequency, multiple orientation 2D symmetrical Gabor wavelet grid that spans the region of importance (ROI). This technique of feature extraction is biologically motivated. The purpose of this study is to demonstrate that localized Gabor wavelet grids with a MLP classifier can be effectively used for recognition of various types of patterns. Recognition of close to 100% is demonstrated for some real world patterns like faces, currency notes, postage stamps and typed characters.
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- 2007
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64. A Back Propagation Based Face Recognition Model, using 2D Symmetrical Gabor Features
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B. Vinay Kumar, B.S. Shreyas, and C.N.S. Ganesh Murthy
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Artificial neural network ,business.industry ,Computer science ,Computer Science::Neural and Evolutionary Computation ,Feature extraction ,Gabor wavelet ,Wavelet transform ,Pattern recognition ,Facial recognition system ,Backpropagation ,ComputingMethodologies_PATTERNRECOGNITION ,Computer Science::Computer Vision and Pattern Recognition ,Multilayer perceptron ,Face (geometry) ,Computer vision ,Artificial intelligence ,business - Abstract
We present a system for recognizing human faces from a database consisting of multiple images per test subject, which spans the normal variations in a human face. The faces are represented based on a Gabor wavelet transform. The features are extracted as a vector of values using a carefully chosen symmetrical Gabor wavelet matrix. This feature extraction is biologically motivated and models systems based on human vision. The extracted features are fed into an artificial neural network, in dual phases. The training and testing phases of the neural network work on the features extracted by the same method. Excellent pattern-recognition-specific neural network like a multilayer perceptron with back propagation provides the necessary classification once the feature extraction is complete
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- 2007
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65. Patient Education and Motivation in Periodontics.
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Sanikop, Mukta V., K., Shiva Charan Yadav, and M. B., Vinay Kumar
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PATIENT education ,PERIODONTICS - Published
- 2017
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66. A Review Over Genetic Algorithm and Application of Wireless Network Systems
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S. B. Vinay Kumar, Bimlendu Shahi, Sujata Dahal, C. Prasanna Kumar, and Abhinav Mishra
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Internet ,Wi-Fi array ,Computer science ,Wireless network ,business.industry ,Distributed computing ,020206 networking & telecommunications ,Wireless WAN ,02 engineering and technology ,Sensor nodes ,Key distribution in wireless sensor networks ,Genetic algorithm ,Sensor node ,0202 electrical engineering, electronic engineering, information engineering ,Mobile wireless sensor network ,General Earth and Planetary Sciences ,Wireless ,020201 artificial intelligence & image processing ,The Internet ,business ,Wireless sensor network ,Heterogeneous network ,General Environmental Science ,Computer network - Abstract
Tele-communication and network industry are becoming extremely fascinated by the use of evolutionary smart sensor nodes in wireless sensor networks. This technology promises to overcome several challenges within WSNs needed for real time data protection via optimization technique: Genetic Algorithm. This paper reviewedthe use of Genetic Algorithms (GAs) to solve certain limitation of wireless sensor networks. It further presents major application areas of wireless sensors networks. Longerdistance gap between a sensor and destination in a sensor network can remarkably reduce the energy of sensors and can degrade the life of a network. GA can prolong the network lifetime by minimizing the total communication distance.
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67. Sustainable synthesis of benzimidazole-based Schiff base using reusable CaAl 2 O 4 nanophosphors catalyst: Insights into metal(II) complexes and DNA interactions.
- Author
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Manjunath M, Sujata FH, Shridhara AH, Vinay Kumar B, Prashantha K, Yogendra K, and Madhusudhana N
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This article presents a new and facile method for the synthesis of Schiff base compounds with a benzimidazole group using a low-cost and reusable calcium aluminate nanophosphorus catalyst (CaAl
2 O4 ). This approach avoids harmful solvents and reactants, supporting a more environmentally friendly synthesis process. The catalyst maintained its activity and heterogeneity over four cycles with minimal loss of efficiency. The synthesis process was straightforward and eliminated the need for column chromatography. The Schiff base ligand (HL=( E )- N -((6-(thiophen-2-yl)pyridin-2-yl)methylene)-1H-benzo[ d ]imidazol-2-amine)) was synthesized by the reaction of 6-(thiophen-2-yl)pyridine-2-carbaldehyde with 1 H -benzimidazole-2-amine. Subsequently, metal(II) complexes of Co(II), Ni(II), and Cu(II) were prepared using this ligand. Structural analysis of both the ligand and its metal complexes was carried out using various physicochemical and spectroscopic methods. Ni(II) and Co(II) complexes were found to adopt an octahedral geometry, while the Cu(II) complex exhibited a square-planar structure. Binding studies with calf thymus DNA (CT-DNA) at pH 7.2 were performed using UV-visible spectroscopy, viscosity measurements, and thermal denaturation studies and showed that the metal complexes intercalate into the DNA and produced a distinct binding pattern. Molecular docking simulations with AutoDock Vina provided insights into the interaction of these complexes with the B-DNA dodecamer. Furthermore, the ligand and its metal complexes showed UV-visible photonuclease activity against pUC19 DNA. Agarose gel electrophoresis showed that the metal complexes exhibit photoinduced nuclease activity, confirming their ability to cleave DNA upon exposure to light.- Published
- 2025
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68. Investigation of bisindole-linked pyrimidine moieties: synthesis using strantium-aluminum supported strontium aluminate nanophosphors catalyst, DNA reactivity, and in silico molecular docking studies.
- Author
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Hanumesh, Amshumali MK, Prachi P, Yogendra K, Madhusudhana N, and Vinay Kumar B
- Abstract
In this communication, an innovative and straightforward protocol for the one-pot catalytic synthesis of bis(indolyl)pyrimidine derivatives and their DNA binding abilities is presented. The synthesis involves the condensation of indole with diverse substituted pyrimidine-5-carbaldehydes, employing cost-effective and reusable Sr-Al supported nanophosphors, specifically strontium aluminate (SrAl
2 O4 ), as a catalyst. In particular, this method does not require the use of toxic solvents. The Sr-Al supported nanophosphorus catalyst exhibited sustained activity over multiple cycles and showed no significant decline while maintaining its strictly heterogeneous properties. The bis(indolyl)pyrimidine derivatives were extensively characterized using spectroscopic and analytical techniques. Furthermore, the interaction between these derivatives and CT-DNA was investigated by absorption spectroscopy, viscosity measurement, and in silico molecular docking studies. Photoinduced cleavage studies demonstrated the photonuclease activity of the compound against pUC19 DNA upon exposure to UV-visible radiation.- Published
- 2024
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69. Fabricate, advancement, molecular docking and DNA reactivity of preferred divalent metal(II) complexes attributing ( E )- N '-((6-hydroxybenzo[ d ]oxazol-5-yl) methylene)isonicotinohydrazide.
- Author
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Pratiba P, Betageri VS, Latha MS, Vinay Kumar B, Ravindranath BS, and Vidyasagar CC
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- DNA chemistry, Isoniazid, Ligands, Molecular Docking Simulation, Schiff Bases chemistry, Coordination Complexes chemistry
- Abstract
A series of metal(II) complexes ( M =Co (II), Ni(II) and Cu(II)) supported by Schiff base ligand ( L =( E )- N '-((6-hydroxybenzo[ d ]oxazol-5-yl)methylene)isonicotinohydrazide) has been designed and developed from condensation of 6-hydroxybenzo[ d ]oxazole-5-carbaldehyde and isoniazid. The ligand (H
2 L) and its metal(II) complexes were structurally characterized utilizing a variety of physicochemical and spectroscopic approaches. The study shows that Schiff bases (H2 L) act as monobasic tridentate ONO ligand and conform to octahedral geometry according to the general formula [M(HL)2 ]. Furthermore, the interaction of these complexes with CT-DNA was investigated at pH = 7.2, utilizing UV-visible absorption, and viscosity measurement. In order to determine the mechanism of binding of the metal(II) complexes to the B-DNA dodecamer, docking studies were conducted using an AutoDock Vina 1.2.0 tool. The photo induced cleavage reveals that the ligand ( H2 L ) and its complexes have UV-visible photo nuclease properties against pUC19 DNA by agarose gel electrophoresis technique. Studies showed that the complexes evaluated firmly bind to CT-DNA via intercalative mode and provides a distinctive pattern of DNA binding.- Published
- 2022
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70. Cashew nutshell liquid catalyzed green chemistry approach for synthesis of a Schiff base and its divalent metal complexes: molecular docking and DNA reactivity.
- Author
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Vidyavathi GT, Vinay Kumar B, Aravinda T, and Hani U
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- Catalysis, Chemistry Techniques, Synthetic, Coordination Complexes chemical synthesis, DNA chemistry, Green Chemistry Technology, Ligands, Nucleic Acid Conformation, Schiff Bases chemistry, Solvents chemistry, Anacardium chemistry, Coordination Complexes chemistry, Coordination Complexes metabolism, DNA metabolism, Molecular Docking Simulation
- Abstract
Cashew Nut Shell Liquid (CNSL) anacardic acid was used, for the first time, as a green and natural effective catalyst for the synthesis of a quinoline based amino acid Schiff base ligand from the condensation of 2-hydroxyquinoline-3-carbaldehyde with l-tryptophan via solvent-free simple physical grinding technique. The use of the nontoxic CNSL natural catalyst has many benefits over toxic reagents and the desired product was obtained in high yield in a short reaction time. The procedure employed is simple and does not involve column chromatography. Moreover, a series of metal(II) complexes (metal = iron(II), cobalt(II), nickel(II), and copper(II)) supported by the synthesized new quinoline based amino acid Schiff base ligand (L) has been designed and the compositions of the metal(II) complexes were examined by various analytical techniques. The findings imply that the 2-hydroxyquinoline-3-carbaldehyde amino acid Schiff base (L) serves as a dibasic tridentate ONO ligand and synchronizes with the metal(II) in octahedral geometry in accordance with the general formula [M(LH)
2 ]. Molecular docking study of the metal(II) complexes with B-DNA dodecamer has revealed good binding energy. The conductivity parameters in DMSO suggest the existence of nonelectrolyte species. The interaction of these metal complexes with CT-DNA has shown strong binding via an intercalative mode with a different pattern of DNA binding, while UV-visible photo-induced molecular cleavage analysis against plasmid DNA using agarose gel electrophoresis has revealed that the metal complexes exhibit photo induced nuclease activity.- Published
- 2021
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71. DNA binding, photoactivated DNA cleavage and cytotoxic activity of Cu(II) and Co(II) based Schiff-base azo photosensitizers.
- Author
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Pradeepa SM, Bhojya Naik HS, Vinay Kumar B, Indira Priyadarsini K, Barik A, and Prabhakara MC
- Subjects
- Animals, Cattle, Electrons, Electrophoresis, Agar Gel, Humans, Inhibitory Concentration 50, MCF-7 Cells, Mass Spectrometry, Nucleic Acid Denaturation drug effects, Proton Magnetic Resonance Spectroscopy, Singlet Oxygen chemistry, Solubility, Spectrophotometry, Infrared, Spectrophotometry, Ultraviolet, Viscosity, Cobalt pharmacology, Copper pharmacology, DNA metabolism, DNA Cleavage drug effects, Photosensitizing Agents pharmacology, Schiff Bases pharmacology
- Abstract
A new class of Cu(II) and Co(II) complexes of azo-containing Schiff base of the type [Cu(L1)2] and [Co(L1)2], where L1=4-[(E)-{2-hydroxy-3-[(E)-(4-bromophenyl)diazenyl]benzylidene}amino]benzoic acid have been synthesized and characterized. Extension of conjugation and the presence of free carboxylic acid group of the ligand L1 increased the wavelength of the complexes from visible region to the near IR region (620-850 nm). The Cu(II) and Co(II) complexes interacted with CT-DNA via intercalative mode with the respective Kb value of 3.2×10(4) M(-1) and 2.9×10(4) M(-1) and acted as proficient photocleavers of SC pUC19 DNA in UV-A light, forming (1)O2 as the reactive oxygen species with the quantum yield of 0.38 and 0.36, respectively. Furthermore, the Cu(II) and Co(II) complexes showed photocytotoxicity toward two selected tumor cell lines MCF-7 and A549 by 3-(4,5-Dimethylthiazol-2-yl)-2,5-diphenyltetrazoliumbromide (MTT) method, and the Cu(II) complex exhibits higher photocytotoxicity than Co(II) complex against each of the selected cell lines, this result is identical with their DNA binding ability order., (Copyright © 2015 Elsevier B.V. All rights reserved.)
- Published
- 2015
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72. Synthesis and biological evaluation of new Tetra-aza macrocyclic scaffold constrained oxadiazole, thiadiazole and triazole rings.
- Author
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Vinay Kumar B, Naik HS, Girija D, Sharath N, Sudeep HV, and Joy Hoskeri H
- Subjects
- Anti-Bacterial Agents chemical synthesis, Anti-Bacterial Agents chemistry, Antioxidants chemical synthesis, Antioxidants chemistry, Antioxidants pharmacology, Bacteria drug effects, Ciprofloxacin pharmacology, DNA drug effects, DNA Replication drug effects, Macrocyclic Compounds chemical synthesis, Macrocyclic Compounds chemistry, Macrocyclic Compounds pharmacology, Microbial Sensitivity Tests, Oxadiazoles chemical synthesis, Oxadiazoles chemistry, Structure-Activity Relationship, Thiadiazoles chemical synthesis, Thiadiazoles chemistry, Triazoles chemical synthesis, Triazoles chemistry, Anti-Bacterial Agents pharmacology, Oxadiazoles pharmacology, Thiadiazoles pharmacology, Triazoles pharmacology
- Abstract
A new series of N,N'-(benzene-1,3-diyldi-1,3,4-oxadiazole-5,2-diyl)bis{2-[(5-benzene-1,3-diyl-1,3,4-oxadiazol-2-yl)amino]acetamide}(macrocycle 1), N,N'-(benzene-1,3-diyldi-1,3,4-thiadiazole-5,2-diyl)bis{2-[(5-benzene-1,3-diyl-1,3,4-thiadiazol-2-yl)amino]acetamide} (macrocycle 2) and S,S'-[benzene-1,3-diylbis(4H-1,2,4-triazole-5,3-diyl)]bis{[(5-benzene-1,3-diyl-4H-1,2,4-triazol-3-yl)sulfanyl]ethanethioate}(macrocycle 3) was synthesized from isophthalic dihydrazide (4) through a multistep reaction sequence. All the synthesized compounds were screened for their inhibitory effect against four different bacterial strains: P. aeruginosa ATCC-20852, K. pneumoniae MTCC-618, S. aureus ATCC- 29737, S. typhi MTCC- 3214. The synthesized compounds showed a significant zone of inhibition and the results were comparable with that of the standard drug ciprofloxacin. The synthesized compounds were further studied for their possible in vitro antioxidant effects by DPPH scavenging, total antioxidant capacity, total reductive capacity and H(2) O(2) scavenging activity. The results indicated that the in vitro antioxidant activity for all the three molecules was efficient when compared to the standards. The DNA interaction behavior of macrocycles 1-3 with CT-DNA was investigated by the absorption spectra obtained (K(b) constant for 1 is 4.53 × 10(4) M(-1) , for 2 is 5.75 × 10(4) M(-1) and for 3 is 5.86 × 10(4) M(-1) ). Based on the results it can be interpreted that the reducing power effect of the newly synthesized compounds demonstrates a direct effect on DNA binding and hence inhibiting the bacterial growth through their action on DNA by inhibiting DNA replication or DNA transcription., (Copyright © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.)
- Published
- 2012
- Full Text
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