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116-58-5

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116-58-5 Usage

Description

20-BETA-DIHYDROCORTISOL, also known as 20β-dihydrocortisol, is a metabolite of cortisol (H714615), a steroid hormone belonging to the glucocorticoid class. It is produced by the zona fasciculata of the adrenal gland and plays a crucial role in the body's response to stress and maintaining blood glucocorticoid levels. The primary functions of 20-BETA-DIHYDROCORTISOL include increasing blood sugar through gluconeogenesis, suppressing the immune system, and aiding in the metabolism of fat, protein, and carbohydrates.

Uses

Used in Diagnostic Applications:
20-BETA-DIHYDROCORTISOL is used as a potential non-invasive diagnostic test for transmissible spongiform encephalopathies (TSEs), a group of progressive neurological disorders that affect both humans and animals. The presence of this metabolite in biological samples can provide valuable information for the early detection and monitoring of TSEs, contributing to improved patient care and management.
Used in Endocrinology and Metabolism Research:
As a metabolite of cortisol, 20-BETA-DIHYDROCORTISOL is used in endocrinology and metabolism research to study the effects of stress on the body and the role of glucocorticoids in various physiological processes. This research can lead to a better understanding of the underlying mechanisms of stress-related disorders and the development of novel therapeutic strategies.
Used in Pharmaceutical Industry:
20-BETA-DIHYDROCORTISOL can be used in the pharmaceutical industry for the development of drugs targeting the glucocorticoid receptor, which plays a key role in regulating the body's response to stress and inflammation. By modulating the activity of this receptor, new drugs can be designed to treat a range of conditions, including autoimmune diseases, inflammatory disorders, and certain types of cancer.
Used in Sports Medicine:
In sports medicine, 20-BETA-DIHYDROCORTISOL can be used as a biomarker to monitor the effects of physical stress and training on the body's endocrine system. This information can help athletes and coaches optimize training regimens, improve performance, and prevent overtraining-related injuries.
Used in Veterinary Medicine:
Similar to its application in human medicine, 20-BETA-DIHYDROCORTISOL can be used in veterinary medicine for the diagnosis and management of TSEs in animals, as well as for studying the effects of stress on the health and well-being of animals. This can contribute to the development of more effective treatment strategies and improved animal welfare.

Check Digit Verification of cas no

The CAS Registry Mumber 116-58-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,1 and 6 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 116-58:
(5*1)+(4*1)+(3*6)+(2*5)+(1*8)=45
45 % 10 = 5
So 116-58-5 is a valid CAS Registry Number.
InChI:InChI=1/C21H32O5/c1-19-7-5-13(23)9-12(19)3-4-14-15-6-8-21(26,17(25)11-22)20(15,2)10-16(24)18(14)19/h9,14-18,22,24-26H,3-8,10-11H2,1-2H3/t14-,15-,16-,17-,18+,19-,20-,21-/m0/s1

116-58-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (8S,9S,10R,11S,13S,14S,17R)-17-[(1R)-1,2-dihydroxyethyl]-11,17-dihydroxy-10,13-dimethyl-2,6,7,8,9,11,12,14,15,16-decahydro-1H-cyclopenta[a]phenanthren-3-one

1.2 Other means of identification

Product number -
Other names 20beta-Dihydrocortisol

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:116-58-5 SDS

116-58-5Downstream Products

116-58-5Relevant articles and documents

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Davoll,Lowy

, p. 1562,1566 (1952)

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Asymmetric reduction of steroidal 20-ketones: Chemical synthesis of corticosteroid derivatives containing the 20α, 21-diol and 17α, 20α, 21-triol side chains

Han,Monder

, p. 619 - 626 (2007/10/02)

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