| Literature DB >> 24344740 |
Jia Liu1, Xiu-Feng He, Gai-Hong Wang, Emilio F Merino, Sheng-Ping Yang, Rong-Xiu Zhu, Li-She Gan, Hua Zhang, Maria B Cassera, He-Yao Wang, David G I Kingston, Jian-Min Yue.
Abstract
Aphadilactones A-D (1-4), four diastereoisomers possessing an unprecedented carbon skeleton, were isolated from the Meliaceae plant Aphanamixis grandifolia. Their challenging structures and absolute configurations were determined by a combination of spectroscopic data, chemical degradation, fragment synthesis, experimental CD spectra, and ECD calculations. Aphadilactone C (3) with the 5S,11S,5'S,11'S configuration showed potent and selective inhibition against the diacylglycerol O-acyltransferase-1 (DGAT-1) enzyme (IC50 = 0.46 ± 0.09 μM, selectivity index > 217) and is the strongest natural DGAT-1 inhibitor discovered to date. In addition, compounds 1-4 showed significant antimalarial activities with IC50 values of 190 ± 60, 1350 ± 150, 170 ± 10, and 120 ± 50 nM, respectively.Entities:
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Year: 2013 PMID: 24344740 DOI: 10.1021/jo402340h
Source DB: PubMed Journal: J Org Chem ISSN: 0022-3263 Impact factor: 4.354