Issue 22, 1989

Biosynthesis of estrogens by microsomal placental aromatase; isolation and metabolism of 10β-hydroxyestr-4-ene-3,17-dione

Abstract

Incubation of [16,16,19-2H3][19-3H]-19-oxoandrost-4-ene-3,17-dione (2a) with microsomal aromatase gave inter alia[16,16-2H2]-10β-hydroxyestr-4-ene-3,17-dione (1), whose analogue (1b) on incubation with the aromatase gave 10β, 17β-dihydroxyestr-4-en-3-one (1d)(ca. 10%) and no estrogens which would indicate that (1b) is not an obligatory estrogen precursor.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1989, 1699-1700

Biosynthesis of estrogens by microsomal placental aromatase; isolation and metabolism of 10β-hydroxyestr-4-ene-3,17-dione

E. Caspi, H. R. W. Dharmaratne and C. Shackleton, J. Chem. Soc., Chem. Commun., 1989, 1699 DOI: 10.1039/C39890001699

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