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Equilenin Impurity 2

N° de SZ CAT SZ-E036004
Número CAS NA
Mol.F. C21H30O2
Peso Molecular 314.5
Status de Fatura Custom Synthesis


Nome Químico: (8R,9S,13S,14S,17R)-13-Methyl-3-propoxy-7,8,9,11,12,13,14,15,16,17-decahydro-6H-cyclopenta[a]phenanthren-17-ol

Sorrisos: C[C@@]1([C@@H]2O)[C@](CC2)([H])[C@@](CCC3=CC(OCCC)=CC=C43)([H])[C@]4([H])CC1

Inchi: InChI=1S/C30H32O2/c1-29-17-15-26-25-14-12-24(31)19-22(25)9-13-27(26)28(29)16-18-30(29,32)23-10-7-21(8-11-23)20-5-3-2-4-6-20/h2-8,10-12,14,19,26-28,31-32H,9,13,15-18H2,1H3/t26-,27-,28+,29+,30-/m1/s1

Formation of equilenin from equilin by porcine adrenals
K. L. Cheo and K. H. Loke
Steroids Volume 11, Issue 5, May 1968, Pages 603-608
 
The Major Metabolite of Equilin, 4-Hydroxyequilin, Autoxidizes to an o-Quinone Which Isomerizes to the Potent Cytotoxin 4-Hydroxyequilenin-o-quinone
Fagen Zhang, Yumei Chen, Emily Pisha, Li Shen, Yansan Xiong, Richard B. van Breemen, and Judy L. Bolton
Chem. Res. Toxicol. 1999, 12, 204-213