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Methylandrostanolone
SpectraBase Compound ID Gm5ZQaag7sT
InChI InChI=1S/C20H32O2/c1-18-9-6-14(21)12-13(18)4-5-15-16(18)7-10-19(2)17(15)8-11-20(19,3)22/h13,15-17,22H,4-12H2,1-3H3/t13-,15+,16-,17-,18-,19-,20-/m0/s1
InChIKey WYZDXEKUWRCKOB-YDSAWKJFSA-N
Mol Weight 304.5 g/mol
Molecular Formula C20H32O2
Exact Mass 304.24023 g/mol
Enantiomer InChIKey WYZDXEKUWRCKOB-KDDXTAFZSA-N
Copyright Copyright © 2014-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample Steraloids Inc.
Source of Spectrum Forensic Spectral Research
Catalog Number A2080-000
Copyright Copyright © 2009-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample Research Plus
Source of Spectrum Forensic Spectral Research
Catalog Number 031-1
Copyright Copyright © 2009-2024 John Wiley & Sons, Inc. All Rights Reserved.
Solvent CDCl3
Copyright Copyright © 2012-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample Research Plus
Source of Spectrum Forensic Spectral Research
Catalog Number 031-1
Copyright Copyright © 2008-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample Research Plus
Source of Spectrum Forensic Spectral Research
Catalog Number 031-1
Technique KBr1 0.56mg
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum SWG-33-1337-0
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum CAY-2023-2077-0
Catalog Number <a href=https://www.caymanchem.com/product/21485>21485</a>
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum O-20-11-1
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum O-20-11-1
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • Mestanolone
  • Methyldihydrotestosterone
  • 5-Androstan-17-methyl-17-ol-3-one
  • 17a-Methylandrostan-17b-ol-3-one
  • 17beta-Hydroxy-17alpha-methyl-5alpha-androstan-3-one
  • Methyl-DHT
  • Mestanolona
  • 17alpha-Methyldihydrotestosterone
  • 17alpha-Methyl-5alpha- androstan-17beta-ol-3-one
  • (5S,8R,9S,10S,13S,14S,17S)-10,13,17-trimethyl-17-oxidanyl-2,4,5,6,7,8,9,11,12,14,15,16-dodecahydro-1H-cyclopenta[a]phenanthren-3-one
Title Journal or Book Year
In-vitro immunomodulatory and anti-cancerous activities of biotransformed products of Dianabol through Azadirachta indica and its molecular docking studies Chemistry Central Journal 2013

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