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Delta-14-Acetophenide Dihydroxyprogesterone

N° de SZ CAT SZ-A018004
Número CAS NA
Mol.F. C29H34O4 
Peso Molecular 446.6
Status de Fatura Custom Synthesis


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

Inchi: InChI=1S/C12H19NO/c1-8(14)13-12-5-9-2-10(6-12)4-11(3-9)7-12/h9-11H,2-7H2,1H3,(H,13,14)

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