Journal of Biological Chemistry · 1966 · 134 citations · 56 references
Life SciencesBiochemistryEndocrinologyEnzymologyMetabolismSteroid BiochemistryGonadal HormonesHormone BiosynthesisHormone MetabolismSteroid BiosynthesisSteroid MetabolismSteroidogenic Enzymes17 Alpha-hydroxylaseAndrogen Conversion EnzymesAndrogen MetabolismGonadal Steroid BiosynthesisNicotinamide Adenine Dinucleotide ReductasesProgesterone CatabolismProgesterone MetabolismSex Steroid Biosynthesis
Exposure of estrone to Nocardia sp. (E 110) resulted in the formation of three degradative products. These have been characterized as 3aα-H-4α-[3'-propanoic acid]-5β-[2-ketopropyl]-7aβ-methyl-1-indanone (Ia), 3aα-H-4α-[3'-propanoic acid]-5β-[4'-but-3-enoic acid]-7aβ-methyl-1-indanone (IIa), and 2-carboxy-7aβ-methyl-7-keto-9aα-H-indano-[5,4f]-5aα,10,10aβ,11-tetrahydroquinoline (IIIa). A plausible mechanism for their formation from estrone is presented.
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Theodore E. Friedemann, Gladys E. Haugen · Journal of Biological Chemistry · 1943 · 1.9K citations · Full text