期刊
JOURNAL OF MEDICINAL CHEMISTRY
卷 45, 期 17, 页码 3569-3572出版社
AMER CHEMICAL SOC
DOI: 10.1021/jm025529g
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A series of 6alpha-alkyl-substituted analogues of chenodeoxycholic acid (CDCA) were synthesized and evaluated as potential farnesoid X receptor (FXR) ligands. Among them, 6alpha-ethyl-chenodeoxycholic acid (6-ECDCA) was shown to be a very potent and selective FXR agonist (EC50 = 99 nM) and to be endowed with anticholeretic activity in an in vivo rat model of cholestasis.
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