Imidazopyridine-based fatty acid synthase inhibitors that show anti-HCV activity and in vivo target modulation

…, L Hu, Y Kosaka, J Lai, M Sivaraja, S Tep…

文献索引：Oslob, Johan D.; Johnson, Russell J.; Cai, Haiying; Feng, Shirley Q.; Hu, Lily; Kosaka, Yuko; Lai, Julie; Sivaraja, Mohanram; Tep, Samnang; Yang, Hanbiao; Zaharia, Cristiana A.; Evanchik, Marc J.; McDowell, Robert S. ACS Medicinal Chemistry Letters, 2013 , vol. 4, # 1 p. 113 - 117

全文：HTML全文

被引用次数: 13

摘要

Potent imidazopyridine-based inhibitors of fatty acid synthase (FASN) are described. The compounds are shown to have antiviral (HCV replicon) activities that track with their biochemical activities. The most potent analogue (compound 19) also inhibits rat FASN and inhibits de novo palmitate synthesis in vitro (cell-based) as well as in vivo.