期刊
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS
卷 22, 期 15, 页码 4994-4997出版社
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.bmcl.2012.06.028
关键词
Hexacyclopeptide; Macrocyclization; Oxa/thiazole; Antimalarial
资金
- ANII [FCE2720]
- CSIC Grupos (UdelaR)
- PEDECIBA
The synthesis of a Microcystis aeruginosa predicted metabolite analog of aerucyclamide B was performed. This hexacyclopeptide was obtained from three heterocyclic building blocks by a convergent macrocycle-assembly methodology. The compound exhibited good in vitro antiplasmodial activity (IC50: 0.18 mu M, K1, cholorquine resistant strain). (c) 2012 Elsevier Ltd. All rights reserved.
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