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Synthesis and antimicrobial evaluation of some pyrazole derivatives.
Molecules (Basel, Switzerland) 20120430
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2-(4-Sulfamoylphen-yl)hydrazin-1-ium chloride.
Acta crystallographica. Section E, Structure reports online 20120401
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4-[5-(Furan-2-yl)-3-trifluoro-methyl-1H-pyrazol-1-yl]benzene-sulfonamide.
Acta crystallographica. Section E, Structure reports online 20120401
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Synthesis and evaluation of anticancer activity of some novel 6-aryl-2-(p-sulfamylphenyl)-pyridazin-3(2H)-ones.
European journal of medicinal chemistry 20120301
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Cloning, characterization and sulfonamide inhibition studies of an α-carbonic anhydrase from the living fossil sponge Astrosclera willeyana.
Bioorganic & medicinal chemistry 20120215
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Synthesis and biological evaluation of some novel sulfamoylphenyl-pyridazinone as anti-inflammatory agents (Part-II * ).
Journal of enzyme inhibition and medicinal chemistry 20120201
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4-(5-Phenyl-3-trifluoro-meth-yl-1H-pyrazol-1--yl)benzene-sulfonamide.
Acta crystallographica. Section E, Structure reports online 20110901
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4-(3-Methyl-5-phenyl-1H-pyrazol-1-yl)benzene-sulfonamide.
Acta crystallographica. Section E, Structure reports online 20110901
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4-(3,5-Dimethyl-1H-pyrazol-1-yl)benzene-sulfonamide.
Acta crystallographica. Section E, Structure reports online 20110901
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4-(5-Oxo-3-phenyl-4,5-dihydro-1H-pyrazol-1-yl)benzene-sulfonamide.
Acta crystallographica. Section E, Structure reports online 20110901
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4-(3-Methyl-4,5-dihydro-1H-benzo[g]indazol-1-yl)benzene-sulfonamide.
Acta crystallographica. Section E, Structure reports online 20110901
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Inhibition studies of the β-carbonic anhydrases from the bacterial pathogen Salmonella enterica serovar Typhimurium with sulfonamides and sulfamates.
Bioorganic & medicinal chemistry 20110815
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A new β-carbonic anhydrase from Brucella suis, its cloning, characterization, and inhibition with sulfonamides and sulfamates, leading to impaired pathogen growth.
Bioorganic & medicinal chemistry 20110201
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Synthesis and biological evaluation of some pyrazolylpyrazolines as anti-inflammatory-antimicrobial agents.
European journal of medicinal chemistry 20100601
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3D-QSAR study of benzene sulfonamide analogs as carbonic anhydrase II inhibitors.
Bioorganic & medicinal chemistry letters 20100515
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Synthesis and biological evaluation of some novel 6-aryl-2-(p-sulfamylphenyl)-4,5-dihydropyridazin-3(2H)-ones as anti-cancer, antimicrobial, and anti-inflammatory agents.
Journal of enzyme inhibition and medicinal chemistry 20100401
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Cloning, characterization, and inhibition studies of a beta-carbonic anhydrase from Brucella suis.
Journal of medicinal chemistry 20100311
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Carbonic anhydrase inhibitors: the beta-carbonic anhydrase from Helicobacter pylori is a new target for sulfonamide and sulfamate inhibitors.
Bioorganic & medicinal chemistry letters 20070701
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Carbonic anhydrase inhibitors. DNA cloning, characterization, and inhibition studies of the human secretory isoform VI, a new target for sulfonamide and sulfamate inhibitors.
Journal of medicinal chemistry 20070125
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Liquid-chromatographic separation and determination of process-related impurities, including a regio-specific isomer of celecoxib on reversed-phase C18 column dynamically coated with hexamethyldisilazane.
Analytical sciences : the international journal of the Japan Society for Analytical Chemistry 20060901
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Carbonic anhydrase inhibitors: cloning and sulfonamide inhibition studies of a carboxyterminal truncated alpha-carbonic anhydrase from Helicobacter pylori.
Bioorganic & medicinal chemistry letters 20060415
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QSAR study on topically acting sulfonamides incorporating GABA moieties: a molecular connectivity approach.
Bioorganic & medicinal chemistry letters 20060401
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Carbonic anhydrase inhibitors: DNA cloning and inhibition studies of the alpha-carbonic anhydrase from Helicobacter pylori, a new target for developing sulfonamide and sulfamate gastric drugs.
Journal of medicinal chemistry 20060323
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Carbonic anhydrase inhibitors. The mitochondrial isozyme VB as a new target for sulfonamide and sulfamate inhibitors.
Journal of medicinal chemistry 20051201
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Carbonic anhydrase inhibitors: inhibition of the transmembrane isozyme XIV with sulfonamides.
Bioorganic & medicinal chemistry letters 20050901
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Carbonic anhydrase inhibitors. Inhibition of the human cytosolic isozyme VII with aromatic and heterocyclic sulfonamides.
Bioorganic & medicinal chemistry letters 20050215
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Carbonic anhydrase inhibitors. Inhibition of the membrane-bound human and bovine isozymes IV with sulfonamides.
Bioorganic & medicinal chemistry letters 20050215
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Carbonic anhydrase inhibitors. Inhibition of the prokariotic beta and gamma-class enzymes from Archaea with sulfonamides.
Bioorganic & medicinal chemistry letters 20041220
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Carbonic anhydrase inhibitors: inhibition of human cytosolic isozyme II and mitochondrial isozyme V with a series of benzene sulfonamide derivatives.
Bioorganic & medicinal chemistry letters 20041115
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Carbonic anhydrase inhibitors: the first QSAR study on inhibition of tumor-associated isoenzyme IX with aromatic and heterocyclic sulfonamides.
Bioorganic & medicinal chemistry letters 20040621
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Carbonic anhydrase inhibitors: inhibition of the tumor-associated isozyme IX with aromatic and heterocyclic sulfonamides.
Bioorganic & medicinal chemistry letters 20030324
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Carbonic anhydrase inhibitors. A general approach for the preparation of water-soluble sulfonamides incorporating polyamino-polycarboxylate tails and of their metal complexes possessing long-lasting, topical intraocular pressure-lowering properties.
Journal of medicinal chemistry 20020328
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Carbonic anhydrase inhibitors: synthesis of sulfonamides incorporating dtpa tails and of their zinc complexes with powerful topical antiglaucoma properties.
Bioorganic & medicinal chemistry letters 20010226