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Volumn 22, Issue 5, 2014, Pages 1586-1595

Carbonic anhydrase inhibitors: Synthesis and inhibition of the human carbonic anhydrase isoforms I, II, IX and XII with benzene sulfonamides incorporating 4- and 3-nitrophthalimide moieties

(7) Sethi, Kalyan K a Verma, Saurabh M a Tanç, Muhammet b Purper, Gaultier b Calafato, Gaetan b Carta, Fabrizio b Supuran, Claudiu T b

a BIRLA INSTITUTE OF TECHNOLOGY (India)

b UNIVERSITY OF FLORENCE (Italy)

Author keywords

Benzenesulfonamide; Docking; Human carbonic anhydrase inhibitors; Nitro 1,3 dioxoisoindolin 2 yl benzenesulfonamide; Sequence alignment; Structure activity relationship

Indexed keywords

2 (4 NITRO 1,3 DIOXOISOINDOLIN 2 YL)BENZENESULFONAMIDE; 2 (5 NITRO 1,3 DIOXOISOINDOLIN 2 YL)BENZENESULFONAMIDE; 3 (4 NITRO 1,3 DIOXOISOINDOLIN 2 YL)BENZENESULFONAMIDE; 3 (5 NITRO 1,3 DIOXOISOINDOLIN 2 YL)BENZENESULFONAMIDE; 4 [(4 NITRO 1,3 DIOXOISOINDOLIN 2 YL)METHYL] BENZENESULFONAMIDE; 4 [(5 NITRO 1,3 DIOXOISOINDOLIN 2 YL)METHYL] BENZENESULFONAMIDE; 4 [2 (5 NITRO 1,3 DIOXOISOINDOLIN 2 YL)ETHYL] BENZENESULFONAMIDE; 4 [2 (5 NITRO 1,3 DIOXOISOINDOLIN 2 YL)ETHYL] BENZENESULFONAMIDE DERIVATIVE; 5 NITRO 1,3 DIOXOISOINDOLIN 2 YL BENZENESULFONAMIDE; ACETAZOLAMIDE; BENZENESULFONAMIDE DERIVATIVE; BRINZOLAMIDE; CARBONATE DEHYDRATASE; CARBONATE DEHYDRATASE INHIBITOR; CELECOXIB; DICLOFENAMIDE; DORZOLAMIDE; ETHOXZOLAMIDE; INDISULAM; ISOENZYME; METHAZOLAMIDE; PHTHALIC ANHYDRIDE; SULFONAMIDE; SULPIRIDE; TOPIRAMATE; UNCLASSIFIED DRUG; VALDECOXIB; ZONISAMIDE; 3-NITROPHTHALIMIDE; BENZENESULFONAMIDE; CARBONATE DEHYDRATASE I; CARBONATE DEHYDRATASE II; ISOINDOLE DERIVATIVE; ISOPROTEIN; ISOQUINOLINE DERIVATIVE;

ARTICLE; DRUG MECHANISM; DRUG STRUCTURE; DRUG SYNTHESIS; ENZYME INHIBITION; MOLECULAR DOCKING; SEQUENCE ALIGNMENT; SEQUENCE HOMOLOGY; STRUCTURE ACTIVITY RELATION; CHEMISTRY; HUMAN; METABOLISM;

CARBONIC ANHYDRASE I; CARBONIC ANHYDRASE II; CARBONIC ANHYDRASE INHIBITORS; HUMANS; ISOINDOLES; ISOQUINOLINES; MOLECULAR DOCKING SIMULATION; PROTEIN ISOFORMS; STRUCTURE-ACTIVITY RELATIONSHIP; SULFONAMIDES;

EID: 84896704335 PISSN: 09680896 EISSN: 14643391 Source Type: Journal
DOI: 10.1016/j.bmc.2014.01.031 Document Type: Article

Times cited : (39)

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