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Equilenin Impurity 1

N° de SZ CAT SZ-E036003
Número CAS 1643577-75-6
Mol.F. C30H32O2
Peso Molecular 424.6
Status de Fatura Custom Synthesis


Nome Químico: (8R,9S,13S,14S,17S)-17-([1,1'-Biphenyl]-4-yl)-13-methyl-7,8,9,11,12,13,14,15,16,17-decahydro-6H-cyclopenta[a]phenanthrene-3,17-diol

Sorrisos: C[C@@]1([C@](O)(C2=CC=C(C3=CC=CC=C3)C=C2)CC4)[C@]4([H])[C@]5([H])CCC6=CC(O)=CC=C6[C@@]5([H])CC1

Inchi: InChI=1S/C9H17NO4.ClH/c1-10(2,3)6-7-14-9(13)5-4-8(11)12;/h4-7H2,1-3H3;1H

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