17974-66-2 Usage
Description
(6R)-6-[(3R,5S,7R,10S,13R)-3,7-dihydroxy-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl]-2-methylheptanoic acid is a complex steroid molecule characterized by its cyclopenta[a]phenanthrene structure and a 6R stereochemistry. This molecule features a long aliphatic side chain and a 2-methylheptanoic acid moiety, indicating potential roles in hormone regulation, metabolism, and lipid-like properties.
Uses
Used in Pharmaceutical Industry:
(6R)-6-[(3R,5S,7R,10S,13R)-3,7-dihydroxy-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl]-2-methylheptanoic acid is used as a biologically active steroid derivative for its potential implications in hormone signaling and lipid metabolism. Its unique structure and properties make it a promising candidate for the development of new drugs targeting hormone-related disorders and metabolic diseases.
Used in Research and Development:
In the field of research and development, this compound is used as a key molecule for studying the effects of steroid hormones on various biological processes. Its complex structure allows scientists to investigate the interactions between hormones and their receptors, as well as the role of lipid metabolism in cellular functions.
Used in Cosmetics Industry:
Due to its potential hormone-regulating properties, (6R)-6-[(3R,5S,7R,10S,13R)-3,7-dihydroxy-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl]-2-methylheptanoic acid may be utilized in the cosmetics industry for the development of products aimed at improving skin health and addressing hormone-related skin conditions.
Used in Agricultural Industry:
The potential hormone-regulating properties of this molecule may also find applications in the agricultural industry, where it could be used to develop new plant growth regulators or to study the effects of hormones on plant growth and development.
Check Digit Verification of cas no
The CAS Registry Mumber 17974-66-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,9,7 and 4 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 17974-66:
(7*1)+(6*7)+(5*9)+(4*7)+(3*4)+(2*6)+(1*6)=152
152 % 10 = 2
So 17974-66-2 is a valid CAS Registry Number.
InChI:InChI=1/C27H46O4/c1-16(6-5-7-17(2)25(30)31)20-8-9-21-24-22(11-13-27(20,21)4)26(3)12-10-19(28)14-18(26)15-23(24)29/h16-24,28-29H,5-15H2,1-4H3,(H,30,31)/t16-,17?,18+,19-,20?,21?,22?,23-,24?,26+,27-/m1/s1
17974-66-2Relevant articles and documents
A convenient synthesis of 5β-cholestan-26-oic and 5β-cholestan-26,27-dioic acids
Starchenkov,Trapencieris,Kauss,Jas,Kalvinsh
, p. 143 - 147 (2000)
A new method for the preparation of 5β-cholestan-26-oic acids 7 and their analogs is described. The key steps in the synthesis are: iodination of bis- and tris-formyloxy-5β-cholan-24-ols 3; nucleophilic substitution of iodides 4 with diethyl sodiomalonate; complete alkaline hydrolysis of esters 5; and subsequent decarboxylation of geminal diacids 6 in DMSO. Copyright (C) 2000 Elsevier Science Inc.
Partial synthesis of stero-bile acids related to chenodeoxycholic acid.
Hoshita,Okuda
, p. 655 - 657 (2007/10/15)
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