Nagahisa A, Spencer R W, Orme-Johnson W H
J Biol Chem. 1983 Jun 10;258(11):6721-3.
The following acetylenic steroids appear to be the first reported mechanism-based inhibitors of cytochrome P-450scc: 20-(1-propynyl)-5-pregnen-3 beta, 20 alpha-diol, 20-(1-hexynyl)-5-pregnen-3 beta, 20 alpha-diol, and 20-(1,5-hexadiynyl)5-pregnen-3 beta, 20 alpha-diol. Oxygen and NADPH are required for enzymatic oxidation and all three steroids yield pregnenolone as a major product. Incubation of P-450scc with 20-(1,5-hexadiynyl)-5-pregnen-3 beta, 20 alpha-diol under turnover conditions completely inactivates the enzyme with a half-time of 11 min. The partition ratio for inactivation by the steroid was determined to be about 6 molecules of the steroid processed per molecule of P-450scc inactivated.
以下炔类甾体似乎是首次报道的基于机制的细胞色素P-450scc抑制剂:20-(1-丙炔基)-5-孕烯-3β,20α-二醇、20-(1-己炔基)-5-孕烯-3β,20α-二醇以及20-(1,5-己二炔基)-5-孕烯-3β,20α-二醇。酶促氧化需要氧气和NADPH,并且所有这三种甾体均产生孕烯醇酮作为主要产物。在周转条件下将P-450scc与20-(1,5-己二炔基)-5-孕烯-3β,20α-二醇一起温育会使该酶完全失活,半衰期为11分钟。已确定该甾体使酶失活的分配比约为每分子失活的P-450scc处理6分子的甾体。