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6beta-Hydroxyfluoxymesterone is a metabolite of Fluoxymesterone, an anabolic steroid with androgenic activity. It is derived from the metabolism of Fluoxymesterone, which is used in the treatment of male hypogonadism and has demonstrated antitumor effects on pregnancy-dependent mammary tumors TPDMT-4.

88936-08-7

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88936-08-7 Usage

Uses

Used in Pharmaceutical Industry:
6beta-Hydroxyfluoxymesterone is used as a pharmaceutical compound for its potential therapeutic effects. As a metabolite of Fluoxymesterone, it may contribute to the treatment of male hypogonadism and could potentially be utilized in the development of treatments for other conditions.
Used in Oncology Research:
6beta-Hydroxyfluoxymesterone is used as a research compound in oncology for its antitumor effects. Its role in the metabolism of Fluoxymesterone, which has shown antitumor activity on pregnancy-dependent mammary tumors TPDMT-4, makes it a valuable candidate for further investigation into its potential as a cancer treatment or supportive therapy.

Check Digit Verification of cas no

The CAS Registry Mumber 88936-08-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,9,3 and 6 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 88936-08:
(7*8)+(6*8)+(5*9)+(4*3)+(3*6)+(2*0)+(1*8)=187
187 % 10 = 7
So 88936-08-7 is a valid CAS Registry Number.

88936-08-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 6β-hydroxyfluoxymesterone

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:88936-08-7 SDS

88936-08-7Upstream product

88936-08-7Downstream Products

88936-08-7Relevant academic research and scientific papers

Metabolism of anabolic steroids in humans: Synthesis of 6β-hydroxy metabolites of 4-chloro-1,2-dehydro-17α-methyltestosterone, fluoxymesterone, and metandienone

Schaenzer, Willi

, p. 353 - 366 (1995)

Hydroxylation at position 6β of testosterone I (17β-hydroxyandrost-4- en-3-one) and the anabolic steroids 17α-methyltestosterone II (17β-hydroxy- 17α-methylandrost-4-en-3-one), metandienone III (17β-hydroxy-17α- methylandrosta-1,4-dien-3-one), 4-chloro-1,2-dehydro-17α-methyltestosterone IV (4-chloro-17β-hydroxy-17α-methylandrosta-1,4-dien-3-one), and fluoxymesterone V (9-fluoro-11β, 17β-dihydroxy-17a-methylandrost-4-en-3- one) was achieved via light-induced autooxidation of the corresponding trimethylsilyl 3,5-dienol ethers dissolved in isopropanol or ethanol. The reaction further yielded the 6α-hydroxy isomer in low amounts. The 6β- hydroxy isomers of I-V and the 6α-hydroxy isomers of I, III, and IV were isolated and characterized by 1H and 13C NMR, high-performance liquid chromatography, gas chromatography, and mass spectrometry. Human excretion studies with single administered doses of boldenone (17β-hydroxyandrosta- 1,4-dien-3-one), 4-chloro-1,2-dehydro-17α-methyltestosterone, fluoxymesterone, metandienone, 17α-methyltestosterone, and [16,16,17- 2H3]testosterone showed that 6β-hydroxylation is the major metabolic pathway in the metabolism of 4-chloro-1,2-dehydro-17α-methyltestosterone, fluoxymesterone, and metandienone, whereas for boldenone, 17α- methyltestosterone, and testosterone, 6β hydroxylation is negligable.

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