SCOPUS 정보 검색 플랫폼

Volumn 21, Issue 6, 2013, Pages 1386-1391

O-Benzenedisulfonimido-sulfonamides are potent inhibitors of the tumor-associated carbonic anhydrase isoforms CA IX and CA XII

(5) Güzel Akdemir, Özlen a Akdemir, Atilla b Isik, Semra c,d Vullo, Daniela d Supuran, Claudiu T d

a ISTANBUL UNIVERSITY (Turkey)

b BEZMIALEM VAKIF UNIVERSITY (Turkey)

c BALIKESIR UNIVERSITY (Turkey)

d UNIVERSITY OF FLORENCE (Italy)

Author keywords

Carbonic anhydrase; Cytosolic isoforms I and II; o Benzenedisulfonimide; Sulfonamide; Tumor associated isoforms IX and XII

Indexed keywords

2 (1,1,3,3 TETRAOXIDO 1,3,2 BENZODITHIAZOL 2 YL)BENZENESULFONAMIDE; 3 (1,1,3,3 TETRAOXIDO 1,3,2 BENZODITHIAZOL 2 YL)BENZENESULFONAMIDE; 3 CHLORO 4 (1,1,3,3 TETRAOXIDO 1,3,2 BENZODITHIAZOL 2 YL)BENZENESULFONAMIDE; 4 (1,1,3,3 TETRAOXIDO 1,3,2 BENZODITHIAZOL 2 YL)BENZENESULFONAMIDE; 4 [(1,1,3,3 TETRAOXIDO 1,3,2 BENZODITHIAZOL 2 YL)METHYL]BENZENESULFONAMIDE; 4 [2 (1,1,3,3 TETRAOXIDO 1,3,2 BENZODITHIAZOL 2 YL)ETHYL]BENZENESULFONAMIDE; ACETAZOLAMIDE; AZACITIDINE; CARBONATE DEHYDRATASE I; CARBONATE DEHYDRATASE II; CARBONATE DEHYDRATASE INHIBITOR; CARBONATE DEHYDRATASE IX; CARBONATE DEHYDRATASE XII; GLYCINE; HISTIDINE; ISOPROTEIN; ORTHO BENZENEDISULFONIMIDO SULFONAMIDE INHIBITOR; SULFONAMIDE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL ANALYSIS; CHEMICAL STRUCTURE; CONTROLLED STUDY; ENZYME ACTIVITY; ENZYME INHIBITION; HUMAN; HYDROGEN BOND; MOLECULAR DOCKING; PROTEIN BINDING;

ACETAZOLAMIDE; ANTIGENS, NEOPLASM; BINDING SITES; CARBONIC ANHYDRASE INHIBITORS; CARBONIC ANHYDRASES; CATALYTIC DOMAIN; HUMANS; IMIDES; KINETICS; MOLECULAR DOCKING SIMULATION; PROTEIN BINDING; SULFONAMIDES;

EID: 84874546224 PISSN: 09680896 EISSN: 14643391 Source Type: Journal
DOI: 10.1016/j.bmc.2012.12.037 Document Type: Article

Times cited : (21)

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