| Literature DB >> 10360737 |
J Lee1, S U Kang, M K Kang, M W Chun, Y J Jo, J H Kwak, S Kim.
Abstract
Four stable analogues of methionyl adenylate (3-6) were designed as inhibitors of methionyl-tRNA synthetase and synthesized from 2',3'-isopropylideneadenosine. They strongly inhibited aminoacylation activity of methionyl-tRNA synthetases isolated from Escherichia coli, Mycobacterium tuberculosis, Saccharomyces cerevisiae and human. Among the microorganisms tested, however, these chemicals showed the growth inhibition effect only on E. coli.Entities:
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Year: 1999 PMID: 10360737 DOI: 10.1016/s0960-894x(99)00206-1
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823