Nome Químico: (16α)-16,17-[[(1R)-1-Phenylethylidene]bis(oxy)]pregn-4-ene-3,20-dione; 2H-Naphth[1',2':6,7]indeno[1,2-d][1,3]dioxole, pregn-4-ene-3,20-dione
Sinônimo: Algestone acetophenide ; Alphasone acetophenide ; Deladroxone ; Dihydroxyprogesterone acetophenide ; Droxone ; Neolutin Depositum
Sorrisos: O=C1C=C(CC[C@]2([H])[C@]3([H])CC[C@@]4(C)[C@@]2([H])C[C@@H](O[C@@](C)(C5=CC=CC=C5)O6)[C@]46C(C)=O)[C@]3(C)CC1
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