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6-BETA,11-ALPHA-DIHYDROXYPROGESTERONE
SpectraBase Compound ID FyZyZYUnohM
InChI InChI=1S/C21H30O4/c1-11(22)14-4-5-15-13-9-17(24)16-8-12(23)6-7-20(16,2)19(13)18(25)10-21(14,15)3/h8,13-15,17-19,24-25H,4-7,9-10H2,1-3H3/t13-,14+,15-,17+,18+,19+,20-,21+/m0/s1
InChIKey KDHBHXVDYRGRDL-KDZLLLCRSA-N
Mol Weight 346.47 g/mol
Molecular Formula C21H30O4
Exact Mass 346.214409 g/mol
Enantiomer InChIKey KDHBHXVDYRGRDL-XFLXTARGSA-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 C5D5N
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent C5D5N
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO-D6
  • 6.BETA.,11.ALPHA.-DIHYDROXY-PREGN-4-ENE-3,20-DIONE
  • (6R,8S,9S,10R,11R,13S,14S,17S)-17-acetyl-6,11-dihydroxy-10,13-dimethyl-6,7,8,9,10,11,12,13,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3(2H)-one
  • 6,11-DIHYDROXYPREGN-4-ENE-3,20-DIONE
Title Journal or Book Year
Biotransformation of progesterone by Absidia griseolla var. igachii and Rhizomucor pusillus Steroids 2012
Predominant allylic hydroxylation at carbons 6 and 7 of 4 and 5-ene functionalized steroids by the thermophilic fungus Rhizomucor tauricus IMI23312 The Journal of Steroid Biochemistry and Molecular Biology 2008
Hydroxylation of progesterone by Cephalosporium aphidicola Phytochemistry 1994

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