| Literature DB >> 10636239 |
C K Han1, S K Ahn, N S Choi, R K Hong, S K Moon, H S Chun, S J Lee, J W Kim, C I Hong, D Kim, J H Yoon, K T No.
Abstract
New fumagillin analogues were designed through structure-based molecular modeling with a human methionine aminopeptidase-2. Among the fumagillin analogues, cinnamic acid ester derivative CKD-731 showed 1000-fold more potent proliferation inhibitory activity on endothelial cell than TNP-470.Entities:
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Year: 2000 PMID: 10636239 DOI: 10.1016/s0960-894x(99)00577-6
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823