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Journal of Molecular Structure

Volumn 605, Issue 1, 2002, Pages 63-70

Crystal structure of a novel synthetic inhibitor of HIV-1 protease

(3) Hilgeroth, Andreas a Tykarska, Ewa b Jaskolski, Mariusz b,c

a MARTIN LUTHER UNIVERSITY HALLE WITTENBERG (Germany)

b ADAM MICKIEWICZ UNIVERSITY (Poland)

c INSTITUTE OF BIOORGANIC CHEMISTRY (Poland)

Author keywords

AIDS; HIV 1 protease inhibition; X ray crystallography

Indexed keywords

1,4 DIHYDROPYRIDINE DERIVATIVE; ASPARTIC ACID DERIVATIVE; BENZYL DERIVATIVE; CARBENE; CYCLOBUTANE; HYDROXYL GROUP; PHENYL GROUP; PIPERIDINE DERIVATIVE; PROTEINASE; PROTEINASE INHIBITOR;

ARTICLE; CRYSTAL STRUCTURE; DIMERIZATION; DRUG BINDING SITE; DRUG CONFORMATION; DRUG SYNTHESIS; ENZYME ACTIVE SITE; ENZYME BINDING; ENZYME INHIBITION; HUMAN IMMUNODEFICIENCY VIRUS 1; HYDROGEN BOND; NONHUMAN; SOLID STATE; X RAY CRYSTALLOGRAPHY;

HUMAN IMMUNODEFICIENCY VIRUS 1;

EID: 0037181042 PISSN: 00222860 EISSN: None Source Type: Journal
DOI: 10.1016/S0022-2860(01)00751-7 Document Type: Article

Times cited : (10)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.