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9-ALPHA-HYDROXY-PROGESTERONE
SpectraBase Compound ID FcOLnW6RBGe
InChI InChI=1S/C21H30O3/c1-13(22)16-6-7-17-18-5-4-14-12-15(23)8-9-20(14,3)21(18,24)11-10-19(16,17)2/h12,16-18,24H,4-11H2,1-3H3/t16-,17+,18+,19-,20+,21-/m1/s1
InChIKey RDBRKMZIODRVBD-LJGAWZCMSA-N
Mol Weight 330.47 g/mol
Molecular Formula C21H30O3
Exact Mass 330.219495 g/mol
Enantiomer InChIKey RDBRKMZIODRVBD-VXAANUECSA-N
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • 9-ALPHA-HYDROXYPREGN-4-ENE-3,20-DIONE
  • PREGN-4-EN-3,20-DIONE-9-ALPHA-OL
Title Journal or Book Year
Microbial transformation of steroids: Contribution to 14α-hydroxylations Steroids 1995
New Hydroxylation Products of Progesterone with Mucor griseocyanus Journal of Natural Products 1987
Microbial hydroxylation of steroids. 10. Rearrangement during epoxidation and hydroxylation, and the stepwise nature of these enzymic reactions Canadian Journal of Chemistry 1985

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