Spiroimidazolidinone NPC1L1 inhibitors. Part 2: Structure–activity studies and in vivo efficacy

Bioorganic & Medicinal Chemistry Letters(2010)

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摘要
Ezetimibe (Zetia®), a cholesterol-absorption inhibitor (CAI) approved by the FDA for the treatment of hypercholesterolemia, is believed to target the intestine protein Niemann-Pick C1-Like 1 (NPC1L1) or its pathway. A spiroimidazolidinone NPC1L1 inhibitor identified by virtual screening showed moderate binding activity but was not efficacious in an in vivo rodent model of cholesterol absorption. Synthesis of analogs established the structure–activity relationships for binding activity, and resulted in compounds with in vivo efficacy, thereby providing proof-of-concept that non-β-lactams can be effective CAIs.
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关键词
Ezetimibe,Cholesterol-absorption inhibitor,Hypercholesterolemia,Niemann-Pick C1-Like 1 protein,Spiroimidazolidinone
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