3862-25-7 Usage
Description
(7R,8S,9S,10R,13R,14S,17R)-7-hydroxy-10,13-dimethyl-17-[(2R)-6-methylheptan-2-yl]-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one is a complex organic compound with a unique molecular structure characterized by its stereochemistry and functional groups. It is a derivative of cyclopenta[a]phenanthrene, featuring a hydroxyl group at the 7-position, two methyl groups at the 10 and 13 positions, and a 6-methylheptan-2-yl group at the 17-position. (7R,8S,9S,10R,13R,14S,17R)-7-hydroxy-10,13-dimethyl-17-[(2R)-6-methylheptan-2-yl]-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one is part of the larger class of triterpenoids, which are known for their diverse biological activities and potential applications in various fields.
Uses
Used in Pharmaceutical Industry:
(7R,8S,9S,10R,13R,14S,17R)-7-hydroxy-10,13-dimethyl-17-[(2R)-6-methylheptan-2-yl]-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one is used as a pharmaceutical agent for its potential therapeutic effects. Its unique structure and functional groups may contribute to its bioactivity, making it a candidate for the development of new drugs targeting various diseases and conditions.
Used in Cosmetic Industry:
In the cosmetic industry, (7R,8S,9S,10R,13R,14S,17R)-7-hydroxy-10,13-dimethyl-17-[(2R)-6-methylheptan-2-yl]-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one may be used as an active ingredient in skincare products due to its potential antioxidant, anti-inflammatory, and moisturizing properties. These properties can contribute to the improvement of skin health and appearance.
Used in Research and Development:
(7R,8S,9S,10R,13R,14S,17R)-7-hydroxy-10,13-dimethyl-17-[(2R)-6-methylheptan-2-yl]-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one is also used in research and development for its potential applications in various fields. Scientists and researchers may study its chemical properties, biological activities, and interactions with other compounds to explore its potential uses in medicine, agriculture, and other industries.
Check Digit Verification of cas no
The CAS Registry Mumber 3862-25-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,8,6 and 2 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 3862-25:
(6*3)+(5*8)+(4*6)+(3*2)+(2*2)+(1*5)=97
97 % 10 = 7
So 3862-25-7 is a valid CAS Registry Number.
InChI:InChI=1/C27H44O2/c1-17(2)7-6-8-18(3)21-9-10-22-25-23(12-14-27(21,22)5)26(4)13-11-20(28)15-19(26)16-24(25)29/h15,17-18,21-25,29H,6-14,16H2,1-5H3/t18-,21-,22+,23+,24-,25+,26+,27-/m1/s1
3862-25-7Relevant articles and documents
Chemical synthesis of 7α-hydroxycholest-4-en-3-one, a biomarker for irritable bowel syndrome and bile acid malabsorption
Offei, Samuel D.,Arman, Hadi D.,Yoshimoto, Francis K.
, (2019/07/31)
7α-Hydroxy-cholest-4-en-3-one is a biomarker for bile acid loss, irritable bowel syndrome, and other diseases associated with defective bile acid biosynthesis. Furthermore, 7α-hydroxy-cholest-4-en-3-one is the physiological substrate for cytochrome P450 8B1 (P450 8B1 or CYP8B1), the oxysterol 12α-hydroxylase enzyme implicated in obesity and cardiovascular health. We report the chemical synthesis of this physiologically important oxysterol beginning with cholesterol. The key feature of this synthesis involves a regioselective C3-allylic oxidation of a 3-desoxy-Δ4-7α-formate steroid precursor to form 7α-formyloxy-cholest-4-en-3-one, which was saponified to yield 7α-hydroxy-cholest-4-en-3-one.
