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5-Beta-Androstan-3-Alpha, 17-Beta-Diol-11-One is a naturally occurring steroid and androgen hormone that plays a crucial role in various physiological processes. As a metabolite of testosterone, it is involved in the development and maintenance of male sexual characteristics, muscle growth, and bone density. This chemical has garnered interest for its potential therapeutic applications in treating muscle wasting and hormone-related disorders, while also being recognized as a banned performance-enhancing substance in competitive sports due to its ability to increase muscle mass and strength.

1158-94-7

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1158-94-7 Usage

Uses

Used in Pharmaceutical Industry:
5-Beta-Androstan-3-Alpha, 17-Beta-Diol-11-One is used as a therapeutic agent for the treatment of certain medical conditions, such as muscle wasting and hormone-related disorders. Its role in promoting muscle growth and maintaining bone density makes it a potential candidate for addressing these health issues.
Used in Sports and Performance Enhancement:
Although banned in competitive sports, 5-Beta-Androstan-3-Alpha, 17-Beta-Diol-11-One is used as a performance-enhancing substance due to its ability to increase muscle mass and strength. Its anabolic effects can provide athletes with a competitive edge, leading to its misuse in the world of sports.

Check Digit Verification of cas no

The CAS Registry Mumber 1158-94-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,5 and 8 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1158-94:
(6*1)+(5*1)+(4*5)+(3*8)+(2*9)+(1*4)=77
77 % 10 = 7
So 1158-94-7 is a valid CAS Registry Number.

1158-94-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name (3R)-3,17-dihydroxy-10,13-dimethyl-1,2,3,4,5,6,7,8,9,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-11-one

1.2 Other means of identification

Product number -
Other names 5|A-Androstane-3|A,17|A-diol-11-one

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:1158-94-7 SDS

1158-94-7Downstream Products

1158-94-7Relevant academic research and scientific papers

The A-ring reduction of 11-ketotestosterone is efficiently catalysed by AKR1D1 and SRD5A2 but not SRD5A1

Barnard, Lise,Nikolaou, Nikolaos,Louw, Carla,Schiffer, Lina,Gibson, Hylton,Gilligan, Lorna C.,Gangitano, Elena,Snoep, Jacky,Arlt, Wiebke,Tomlinson, Jeremy W.,Storbeck, Karl-Heinz

, (2020)

Testosterone and its 5α-reduced form, 5α-dihydrotestosterone, were previously thought to represent the only active androgens in humans. However, recent studies have shown that the potent androgen, 11-ketotestosterone, derived from the adrenal androgen precursor, 11β-hydroxyandrostenedione, may in fact serve as the primary androgen in healthy women. Yet, despite recent renewed interest in these steroids, their downstream metabolism has remained undetermined. We therefore set out to investigate the metabolism of 11-ketotestosterone by characterising the 5α- or 5β-reduction commitment step. We show that inactivation of 11-ketotestosterone is predominantly driven by AKR1D1, which efficiently catalyses the 5β-reduction of 11-ketotestosterone, committing it to a metabolic pathway that terminates in 11-ketoetiocholanolone. We demonstrate that 5α-reduction of 11-ketotestosterone is catalysed by SRD5A2, but not SRD5A1, and terminates in 11-ketoandrosterone, but is only responsible for a minority of 11-ketotestosterone inactivation. However, as 11-ketoetiocholanolone is also generated by the metabolism of the glucocorticoid cortisone, 11-ketoandrosterone should be considered a more specific urinary marker of 11-ketotestosterone production.

Steroid transformations with Exophiala jeanselmei var. lecanii-corni and Ceratocystis paradoxa

Porter, Roy B.R.,Gallimore, Winklet A.,Reese, Paul B.

, p. 770 - 779 (2007/10/03)

The fungi Exophiala jeanselmei var. lecanii-corni [IMI (International Mycological Institute) 312989, UAMH (University of Alberta Microfungus Collection and Herbarium) 8783] and Ceratocystis paradoxa (IMI 374529, UAMH 8784) have been examined for their potential in steroid biotransformation. The study has determined that E. jeanselmei var. lecanii-corni effected overall anti-Markovnikov hydration on dehydroisoandrosterone, and side-chain degradation on a variety of pregnanes. Both ascomycetes were found to carry out redox reactions of alcohols and ketones as well as 1,4 reduction of α,β-unsaturated carbonyl systems.

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