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Bioorganic and Medicinal Chemistry Letters

Volumn 20, Issue 15, 2010, Pages 4376-4381

Carbonic anhydrase inhibitors. the X-ray crystal structure of human isoform II in adduct with an adamantyl analogue of acetazolamide resides in a less utilized binding pocket than most hydrophobic inhibitors

(7) Avvaru, Balendu Sankara a Wagner, Jason M a Maresca, Alfonso b Scozzafava, Andrea b Robbins, Arthur H a Supuran, Claudiu T b McKenna, Robert a

a UNIVERSITY OF FLORIDA COLLEGE OF MEDICINE (United States)

b UNIVERSITY OF FLORENCE (Italy)

Author keywords

1,3,4 Thiadiazole 2 sulfonamide; Carbonic anhydrase; Enzyme inhibitor; Isoforms I XV; Sulfonamide; X ray crystallography

Indexed keywords

1,3,4 THIADIAZOLE DERIVATIVE; ACETAZOLAMIDE; CARBONATE DEHYDRATASE I; CARBONATE DEHYDRATASE II; CARBONATE DEHYDRATASE III; CARBONATE DEHYDRATASE INHIBITOR; CARBONATE DEHYDRATASE IV; CARBONATE DEHYDRATASE IX; CARBONATE DEHYDRATASE V; CARBONATE DEHYDRATASE XII; ISOLEUCINE; PHENYLALANINE; SULFONAMIDE; VALINE;

ARTICLE; CRYSTAL STRUCTURE; ENZYME ACTIVE SITE; HYDROPHOBICITY; X RAY CRYSTALLOGRAPHY;

ACETAZOLAMIDE; ANIMALS; BINDING SITES; CARBONIC ANHYDRASE II; CARBONIC ANHYDRASE INHIBITORS; COMPUTER SIMULATION; CRYSTALLOGRAPHY, X-RAY; HUMANS; HYDROPHOBIC AND HYDROPHILIC INTERACTIONS; MICE; PROTEIN ISOFORMS; SULFONAMIDES;

EID: 77955424033 PISSN: 0960894X EISSN: None Source Type: Journal
DOI: 10.1016/j.bmcl.2010.06.082 Document Type: Article

Times cited : (69)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.