化学名称: 1-((3S,8R,9S,10R,13S,14S)-3-Hydroxy-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15-dodecahydro-1Hcyclopenta[a]phenanthren-17-yl)ethanone Hydrochloride
微笑: C[C@@]12[C@](CC=C2C(C)=O)([H])[C@]3([H])CC=C4C[C@@H](O)CC[C@]4(C)[C@@]3([H])CC1.Cl
印地语: InChI=1S/C21H30O4.H/c1-12(22)21(25)18(24)11-17-15-5-4-13-10-14(23)6-8-19(13,2)16(15)7-9-20(17,21)3;/h10,15-18,24-25H,4-9,11H2,1-3H3;/t15-,16+,17+,18-,19+,20+,21-;/m1./s1/i;1+1
Mechanism of 17α,20-lyase and new hydroxylation reactions of human cytochrome p450 17a1: 18o labeling and oxygen surrogate evidence for a role of a perferryl oxygen
Francis K.Yoshimoto, EricGonzalez, Richard J.Auchus§F. PeterGuengerich
Journal of Biological Chemistry Volume 291, Issue 33, 12 August 2016, Pages 17143-17164