SpectraBase Compound ID | 94P1FLQ5KFm |
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InChI | InChI=1S/C19H28O2/c1-18-9-7-13(20)11-12(18)3-4-14-15-5-6-17(21)19(15,2)10-8-16(14)18/h11,14-17,21H,3-10H2,1-2H3/t14-,15-,16-,17-,18-,19-/m0/s1 |
InChIKey | MUMGGOZAMZWBJJ-DYKIIFRCSA-N |
Mol Weight | 288.43 g/mol |
Molecular Formula | C19H28O2 |
Exact Mass | 288.20893 g/mol |
Enantiomer InChIKey | MUMGGOZAMZWBJJ-MGYGNFHQSA-N |
Copyright | Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved. |
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Source of Spectrum | CAY-2023-426-0 |
Catalog Number | ISO60154 |
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 |
Metabolism of anabolic steroids in humans: Synthesis of 6β-hydroxy metabolites of 4-chloro-1,2-dehydro-17α-methyltestosterone, fluoxymesterone, and metandienone | Steroids | 1995 |
Microbial transformation of steroids: Contribution to 14α-hydroxylations | Steroids | 1995 |
13C n.m.r. spectra of steroids —a survey and commentary | Organic Magnetic Resonance | 1977 |
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