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ChemMedChem

Volumn 2, Issue 7, 2007, Pages 1015-1029

Rational design, synthesis, and evaluation of nanomolar type II dehydroquinase inhibitors

(5) Payne, Richard J a Peyrot, Fabienne a Kerbarh, Olivier a Abell, Andrew D b Abell, Chris a

a UNIVERSITY OF CAMBRIDGE (United Kingdom)

b UNIVERSITY OF CANTERBURY (New Zealand)

Author keywords

Antimicrobials; Cross coupling; Dehydroquinase inhibitors; Tuberculosis

Indexed keywords

3 DEHYDROQUINATE DEHYDRATASE; 3-DEHYDROQUINATE DEHYDRATASE; ENZYME INHIBITOR; HYDROLYASE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL STRUCTURE; CHEMISTRY; CONFORMATION; DRUG ANTAGONISM; DRUG DESIGN; DRUG SCREENING; MASS SPECTROMETRY; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; SYNTHESIS;

DRUG DESIGN; DRUG EVALUATION, PRECLINICAL; ENZYME INHIBITORS; HYDRO-LYASES; MAGNETIC RESONANCE SPECTROSCOPY; MASS SPECTROMETRY; MODELS, MOLECULAR; MOLECULAR CONFORMATION;

EID: 37349074787 PISSN: 18607179 EISSN: 18607187 Source Type: Journal
DOI: 10.1002/cmdc.200700032 Document Type: Article

Times cited : (30)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.