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6-BETA,14-ALPHA-DIHYDROXY-PROGESTERONE
SpectraBase Compound ID JyBIhiU6czi
InChI InChI=1S/C21H30O4/c1-12(22)14-6-9-21(25)16-11-18(24)17-10-13(23)4-7-19(17,2)15(16)5-8-20(14,21)3/h10,14-16,18,24-25H,4-9,11H2,1-3H3/t14-,15+,16-,18-,19-,20-,21-/m1/s1
InChIKey LQCNIUSTCXGYKI-PIABYFCUSA-N
Mol Weight 346.47 g/mol
Molecular Formula C21H30O4
Exact Mass 346.214409 g/mol
Enantiomer InChIKey LQCNIUSTCXGYKI-DLQWHNFBSA-N
Copyright Copyright © 2011-2024 Wiley-VCH GmbH. All Rights Reserved.
Source of Spectrum Prof. Spiteller, University Bayreuth, Germany
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:CD3OD=1:1
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CD3OD
  • 6-BETA,14-ALPHA-DIHYDROXYPREGN-4-ENE-3,20-DIONE
  • (6R,8R,9S,10R,13R,14R,17S)-17-acetyl-6,14-dihydroxy-10,13-dimethyl-6,7,8,9,10,11,12,13,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3(2H)-one
  • 6,14-DIHYDROXYPREGN-4-ENE-3,20-DIONE
Title Journal or Book Year
Biotransformation of progesterone by Absidia griseolla var. igachii and Rhizomucor pusillus Steroids 2012
Microbial transformation of steroids: Contribution to 14α-hydroxylations Steroids 1995
New Hydroxylation Products of Progesterone with Mucor griseocyanus Journal of Natural Products 1987

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