Novel 3-phenylprop-2-ynylamines as inhibitors of mammalian squalene epoxidaseElectronic supplementary information (ESI) available: Proton NMR spectra for the intermediate piperidines 56–60 and acetylenes 63-81 and 85,86. See http://www.rsc.org/suppdata/ob/b2/b209165h/
作者:David L. Musso、Morris J. Clarke、James L. Kelley、G. Evan Boswell、Grace Chen
DOI:10.1039/b209165h
日期:2003.1.30
The synthesis of a novel series of 3-phenylprop-2-ynylamines as selective mammalian squalene epoxidase inhibitors is described. Structure–activity relationship studies led to the discovery of compound 19, 1-[3-(3,5-dichlorophenyl)prop-2-ynyl]-3-methylpiperidine hydrochloride with an IC50 of 2.8 ± 0.6 µM against rat liver squalene epoxidase. Against 23 strains of fungal squalene epoxidase compound 19 was found to be inactive.
报道了一种新型3-苯基丙-2-炔基胺系列化合物的合成,这些化合物是选择性哺乳动物角鲨烯环氧化酶抑制剂。构效关系研究表明,化合物19,即1-[3-(3,5-二氯苯基)丙-2-炔基]-3-甲基哌啶盐酸盐,对大鼠肝脏角鲨烯环氧化酶的IC50值为2.8 ± 0.6 µM。化合物19对23株真菌角鲨烯环氧化酶未显示出活性。