期刊
JOURNAL OF MEDICINAL CHEMISTRY
卷 54, 期 13, 页码 4880-4895出版社
AMER CHEMICAL SOC
DOI: 10.1021/jm200484c
关键词
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The development of the structure-activity studies leading to the discovery of anacetrapib is described. These studies focused on varying the substitution of the oxazolidinone ring of the 5-aryloxazolidinone system. Specifically, it was found that substitution of the 4-position with a methyl group with the cis-stereochemistry relative to the 5-aryl group afforded compounds with increased cholesteryl ester transfer protein (CETP) inhibition potency and a robust in vivo effect on increasing HDL-C levels in transgenic mice expressing cynomolgus monkey CETP.
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