8,235 results on '"Supuran, Claudiu T."'
Search Results
52. A simple yet multifaceted 90 years old, evergreen enzyme: Carbonic anhydrase, its inhibition and activation
53. Substituted furan sulfonamides as carbonic anhydrase inhibitors: Synthesis, biological and in silico studies
54. The roles of plasma accessible and cytosolic carbonic anhydrases in bicarbonate (HCO3−) excretion in Pacific hagfish (Eptatretus stoutii)
55. Morphologic design of nanogold carriers for a carbonic anhydrase inhibitor: Effect on ocular retention and intraocular pressure
56. Escinosome thermosensitive gel optimizes efficacy of CAI-CORM in a rat model of rheumatoid arthritis
57. Arylidine extensions of 3-methyl-5-oxo-4,5-dihydro-1H-pyrazol-benzenesulfonamide derivatives: Synthesis, computational simulations and biological evaluation as tumor-associated carbonic anhydrase inhibitors
58. A new way of synthesizing heterocyclic primary sulfonamide probes for carbonic anhydrase
59. A novel acidification mechanism for greatly enhanced oxygen supply to the fish retina.
60. An insight into the biological activity and structure-based drug design attributes of sulfonylpiperazine derivatives
61. PET radiotracers and fluorescent probes for imaging human carbonic anhydrase IX and XII in hypoxic tumors
62. 4-(5-Amino-pyrazol-1-yl)benzenesulfonamide derivatives as novel multi-target anti-inflammatory agents endowed with inhibitory activity against COX-2, 5-LOX and carbonic anhydrase: Design, synthesis, and biological assessments
63. Schiff bases as linker in the development of quinoline-sulfonamide hybrids as selective cancer-associated carbonic anhydrase isoforms IX/XII inhibitors: A new regioisomerism tactic
64. Biochemical and Biophysical Characterization of Carbonic Anhydrase VI from Human Milk and Saliva
65. Contributors
66. Advances in the discovery of novel agents for the treatment of glaucoma: The role of nitric oxide donors
67. Phenols and Polyphenols as Carbonic Anhydrase Inhibitors
68. Coumarins as Carbonic Anhydrase Inhibitors
69. Development of potent nanosized carbonic anhydrase inhibitor for targeted therapy of hypoxic solid tumors
70. Design, synthesis, biological evaluation and crystal structure determination of dual modulators of carbonic anhydrases and estrogen receptors
71. Inhibition of nicotinamide phosphoribosyltransferase (NAMPT) in cancer: a patent review
72. Management of Neisseria gonorrhoeae infection: from drug resistance to drug repurposing
73. Biomedical applications of prokaryotic carbonic anhydrases: an update
74. Isocoumarins incorporating chalcone moieties act as isoform selective tumor-associated carbonic anhydrase inhibitors
75. Novel 2,4-Dichloro-5-sulfamoylbenzoic Acid Oxime Esters: First Studies as Potential Human Carbonic Anhydrase Inhibitors
76. Mechanistic modeling of Mycobacterium tuberculosis β-carbonic anhydrase inhibitors using integrated systems biology and the QSAR approach
77. Anticancer drugs: where are we now?
78. Phthalazine sulfonamide derivatives as carbonic anhydrase inhibitors. Synthesis, biological and in silico evaluation
79. In‐vitro and in‐silico investigations of SLC‐0111 hydrazinyl analogs as human carbonic anhydrase I, II, IX, and XII inhibitors
80. The production and biochemical characterization of α-carbonic anhydrase from Lactobacillus rhamnosus GG
81. New β-arylchalcogeno amines with procognitive properties targeting Carbonic Anhydrases and Monoamine Oxidases
82. Carbonic Anhydrase inhibitors bearing organotelluride moieties as novel agents for antitumor therapy
83. Development of benzene and benzothiazole-sulfonamide analogues as selective inhibitors of the tumor-associated carbonic anhydrase IX
84. Sulfonamide diuretic azosemide as an efficient carbonic anhydrase inhibitor
85. Investigation of carbonic anhydrase inhibitory effects and cytotoxicities of pyrazole-based hybrids carrying hydrazone and zinc-binding benzenesulfonamide pharmacophores
86. Application of LEDA algorithm for the recognition of P-glycoprotein and Carbonic Anhydrase hybrid inhibitors and evaluation of their plasma stability by HPLC-MS/MS analysis
87. A decade of tail-approach based design of selective as well as potent tumor associated carbonic anhydrase inhibitors
88. Insights into the effect of elaborating coumarin-based aryl enaminones with sulfonamide or carboxylic acid functionality on carbonic anhydrase inhibitory potency and selectivity
89. Development of 4-((3-oxo-3-phenylpropyl)amino)benzenesulfonamide derivatives utilizing tail/dual-tail approaches as novel carbonic anhydrase inhibitors
90. Chlorinated benzothiadiazines inhibit angiogenesis through suppression of VEGFR2 phosphorylation
91. Heterobimetallic complexes containing organometallic acylhydrazone ligands as potential inhibitors of human carbonic anhydrases
92. Tail-approach based design and synthesis of Arylthiazolylhydrazono-1,2,3-triazoles incorporating sulfanilamide and metanilamide as human carbonic anhydrase I, II, IV and IX inhibitors
93. Benzoselenoates: A novel class of carbonic anhydrase inhibitors
94. Post-translational modifications in tumor-associated carbonic anhydrases
95. Synthesis and anticancer activity of new benzensulfonamides incorporating s-triazines as cyclic linkers for inhibition of carbonic anhydrase IX
96. Inhibition of carbonic anhydrases IX/XII by SLC-0111 boosts cisplatin effects in hampering head and neck squamous carcinoma cell growth and invasion
97. Exploration of 2-phenylquinoline-4-carboxamide linked benzene sulfonamide derivatives as isoform selective inhibitors of transmembrane human carbonic anhydrases
98. Discovery of new carbonic anhydrase IX inhibitors as anticancer agents by toning the hydrophobic and hydrophilic rims of the active site to encounter the dual-tail approach
99. An innovative spectroscopic approach for qualitative and quantitative evaluation of Mb-CO from myoglobin carbonylation reaction through chemometrics methods
100. Enhanced Recognition Memory through Dual Modulation of Brain Carbonic Anhydrases and Cholinesterases.
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.