化学名称: (16α)-16,17-[(1-Methylethylidene)bis(oxy)]pregn-4-ene-3,20-dione; 16α,17-(Isopropylidenedioxy)progesterone; 16α,17-Dihydroxypregn-4-ene-3,20-dione cyclic acetal with acetone; 16α,17α-Isopropylidenedioxyprogesterone
异名: Algestone acetonide ; Alphasone acetonide ; Progesterone 16,17-acetonide
微笑: CC([C@]([C@@]1([H])C[C@@]2([H])[C@@](CCC3=CC4=O)([H])[C@]([C@]3(CC4)C)([H])CC5)(OC(C)(C)O1)[C@]25C)=O
印地语: InChI=1S/C21H30O4/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
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