M7655

Mesterolone

Name: Mesterolone
Brand: SIAL
Price: 75.75 USD

analytical standard

Synonym(s):

1α-Methylandrostan-17β-ol-3-one

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100 MG

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About This Item

Empirical Formula (Hill Notation):

C₂₀H₃₂O₂

CAS Number:

1424-00-6

Molecular Weight:

304.47

EC Number:

215-836-3

MDL number:

MFCD00133082

UNSPSC Code:

41116107

PubChem Substance ID:

329817913

NACRES:

NA.24

Key Documents

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grade

analytical standard

Quality Level

200

drug control

USDEA Schedule III; Home Office Schedule 4.2; regulated under CDSA - not available from Sigma-Aldrich Canada

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

forensics and toxicology
pharmaceutical (small molecule)
veterinary

format

neat

SMILES string

[H][C@@]12CC[C@@]3([H])[C@]4([H])CC[C@H](O)[C@@]4(C)CC[C@]3([H])[C@@]1(C)[C@@H](C)CC(=O)C2

InChI

1S/C20H32O2/c1-12-10-14(21)11-13-4-5-15-16-6-7-18(22)19(16,2)9-8-17(15)20(12,13)3/h12-13,15-18,22H,4-11H2,1-3H3/t12-,13-,15-,16-,17-,18-,19-,20-/m0/s1

InChI key

UXYRZJKIQKRJCF-TZPFWLJSSA-N

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This Item	46923	T3925	T6501
Supelco M7655 Mesterolone	Supelco 46923 Testosterone	Supelco T3925 Trenbolone	Supelco T6501 Triamcinolone acetonide
application(s) forensics and toxicology pharmaceutical (small molecule) veterinary	application(s) forensics and toxicology pharmaceutical (small molecule)	application(s) forensics and toxicology pharmaceutical (small molecule) veterinary	application(s) forensics and toxicology pharmaceutical (small molecule) veterinary
technique(s) HPLC: suitable, gas chromatography (GC): suitable	technique(s) HPLC: suitable, gas chromatography (GC): suitable	technique(s) HPLC: suitable, gas chromatography (GC): suitable	technique(s) HPLC: suitable, gas chromatography (GC): suitable
Quality Level 200	Quality Level 100	Quality Level 200	Quality Level 100
grade analytical standard	grade analytical standard	grade analytical standard, for drug analysis	grade analytical standard
drug control USDEA Schedule III; Home Office Schedule 4.2; regulated under CDSA - not available from Sigma-Aldrich Canada	drug control USDEA Schedule IIIN; regulated under CDSA - not available from Sigma-Aldrich Canada	drug control USDEA Schedule III; Home Office Schedule 4.2; regulated under CDSA - not available from Sigma-Aldrich Canada	drug control -
format neat	format neat	format neat	format neat

Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

pictograms

GHS08,GHS09

signalword

Danger

hcodes

H351,H360FD,H362,H411

pcodes

P202 - P260 - P263 - P264 - P273 - P308 + P313

Hazard Classifications

Aquatic Chronic 2 - Carc. 2 - Lact. - Repr. 1B

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Hepatocyte nuclear phenotype: the cross-talk between anabolic androgenic steroids and exercise in transgenic mice.

Karina Fontana et al.

Histology and histopathology, 23(11), 1367-1377 (2008-09-12)

The growing and indiscriminate use of high doses of anabolic androgenic steroid (AAS) among youth and athletes has raised serious concerns about its hepatotoxic effects. Herein, the influence of AAS in the nuclear phenotype of hepatocytes was investigated in sedentary

The discovery of antidepressant drugs by computer-analyzed human cerebral bio-electrical potentials (CEEG).

T M Itil

Progress in neurobiology, 20(3-4), 185-249 (1983-01-01)

Antidepressant properties of six compounds were predicted based on their computer-analyzed human electroencephalographical (CEEG) profiles. The clinical investigations with mianserin (GB-94) confirmed the CEEG prediction. This compound has now been marketed as the first antidepressant of which the clinical effects

Metabolic studies of mesterolone in horses.

Emmie N M Ho et al.

Analytica chimica acta, 596(1), 149-155 (2007-07-10)

Mesterolone (1alpha-methyl-5alpha-androstan-17beta-ol-3-one) is a synthetic anabolic androgenic steroid (AAS) with reported abuses in human sports. As for other AAS, mesterolone is also a potential doping agent in equine sports. Metabolic studies on mesterolone have been reported for humans, whereas little

Microbial oxidation of anabolic steroids.

M Iqbal Choudhary et al.

Natural product research, 22(15), 1289-1296 (2008-11-22)

Microbial transformation of two anabolic steroids, ethylestrenol (1) and nandrolone (2), were carried out. Ethylestrenol (1), when incubated with Rhizopus stolonifer (TSY 0471), yielded two oxidative metabolites named 17alpha-ethyl-3beta,17beta-dihydroxy-19-norndrost-4-ene (3) and 17alpha-ethyl-17beta-hydroxy-19-norandrost-4-en-3-one (4), while incubation of compound 2 with the

Human androgen receptor mutation disrupts ternary interactions between ligand, receptor domains, and the coactivator TIF2 (transcription intermediary factor 2).

J Lim et al.

Molecular endocrinology (Baltimore, Md.), 14(8), 1187-1197 (2000-08-10)

The androgen receptor (AR) is a ligand-dependent X-linked nuclear transcription factor regulating male sexual development and spermatogenesis. The receptor is activated when androgen binds to the C-terminal ligand-binding domain (LBD), triggering a cascade of molecular events, including interactions between the

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Mesterolone