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7-ALPHA-HYDROXY-ANDROST-4-EN-3,17-DIONE
SpectraBase Compound ID Ey34jcWO6mh
InChI InChI=1S/C19H26O3/c1-18-7-5-12(20)9-11(18)10-15(21)17-13-3-4-16(22)19(13,2)8-6-14(17)18/h9,13-15,17,21H,3-8,10H2,1-2H3/t13-,14-,15+,17-,18-,19-/m0/s1
InChIKey LFWLQMQUJQUZBD-TYHLISGHSA-N
Mol Weight 302.41 g/mol
Molecular Formula C19H26O3
Exact Mass 302.188195 g/mol
Enantiomer InChIKey LFWLQMQUJQUZBD-BENAYJGTSA-N
Copyright Copyright © 2011-2024 Wiley-VCH GmbH. All Rights Reserved.
Source of Spectrum Dr. Makin, London Hospital Medical College, UK
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 C5D5N
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • 7-ALPHA-HYDROXY-ANDROST-4-ENE-3,17-DIONE
  • ANDROST-4-ENE-3,17-DIONE-7-ALPHA-OL
  • ANDROST-4-ENE-7.ALPHA.-OL-3,17-DIONE
  • (7R,8R,9S,10R,13S,14S)-7-hydroxy-10,13-dimethyl-7,8,9,10,11,12,13,14,15,16-decahydro-1H-cyclopenta[a]phenanthrene-3,17(2H,6H)-dione
  • 7-HYDROXYANDROST-4-ENE-3,17-DIONE
Title Journal or Book Year
An unusual ring—A opening and other reactions in steroid transformation by the thermophilic fungus Myceliophthora thermophila The Journal of Steroid Biochemistry and Molecular Biology 2009
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
Microbial transformation of steroids: Contribution to 14α-hydroxylations Steroids 1995
Microbial hydroxylation of steroids. 8. Incubation of Cn halo- and other substituted steroids with Cn hydroxylating fungi Canadian Journal of Chemistry 1982

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