Nome Químico: (6aR,6bS,8aS,8bS,11aR,12bR)-8b-Acetyl-6a,8a,10-trimethyl-10-phenyl-1,2,5,6,6a,6b,7,8,8a,8b,11a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one
Sorrisos: O=C1C=C(CC[C@]2([H])[C@]3([H])CC[C@@]4(C)C2=C[C@@H](OC(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
