84413-81-0 Usage
Description
(4R)-4-[(5S,7S,8S,9S,10S,12S,13R,14S,17R)-7,12-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]pentanoic acid is a steroidal compound that is a derivative of cyclopenta[a]phenanthren-17-yl pentanoic acid. It features a specific (4R) configuration and a complex tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl core with multiple hydroxy and methyl substituents at various positions. (4R)-4-[(5S,7S,8S,9S,10S,12S,13R,14S,17R)-7,12-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]pentanoic acid contains a cyclopenta[a]phenanthrene core and a carboxylic acid group, which may contribute to its potential biological activity and use in research or drug development.
Uses
Used in Pharmaceutical Research:
(4R)-4-[(5S,7S,8S,9S,10S,12S,13R,14S,17R)-7,12-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]pentanoic acid is used as a research compound for exploring its potential biological activity and applications in drug development. Its unique structure and stereochemistry may offer insights into the development of new therapeutic agents.
Used in Drug Development:
In the pharmaceutical industry, (4R)-4-[(5S,7S,8S,9S,10S,12S,13R,14S,17R)-7,12-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]pentanoic acid is used as a lead compound for the development of new drugs. Its complex structure and the presence of hydroxy and methyl groups may provide opportunities for optimization and the discovery of novel therapeutic agents with improved efficacy and selectivity.
Check Digit Verification of cas no
The CAS Registry Mumber 84413-81-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,4,1 and 3 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 84413-81:
(7*8)+(6*4)+(5*4)+(4*1)+(3*3)+(2*8)+(1*1)=130
130 % 10 = 0
So 84413-81-0 is a valid CAS Registry Number.
InChI:InChI=1/C24H40O4/c1-14(7-10-21(27)28)16-8-9-17-22-18(13-20(26)24(16,17)3)23(2)11-5-4-6-15(23)12-19(22)25/h14-20,22,25-26H,4-13H2,1-3H3,(H,27,28)/t14-,15+,16-,17+,18+,19+,20+,22+,23+,24-/m1/s1
84413-81-0Relevant articles and documents
DARSTELLUNG VON CHOLSAEURELACTONEN
Schulze, P. E.,Seeger, A.,Illi, V.
, p. 2815 - 2818 (2007/10/02)
The 8-membered cyclic 24,12-lactones of cholic- and deoxycholic acid, previously prepared only in poor yield are easily synthesized by the reaction of the appropriate acids with arylsulfonylchloride in pyridine.Chenodeoxycholic acid is converted into a di
Intramolecular catalysis. VI. Selectivity in 7 ,12 -dihydroxy steroids and enhancement of 12 -hydroxyl reactivity by substituents at carbon 3.
Wolf,Foster,Blickenstaff
, p. 1276 - 1279 (2007/10/13)
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