CAS 53608-86-9
:(3R)-3-[(3R,5R,8R,9S,10S,12S,13R,14S,17R)-3,12-dihydroxy-10,13-dimethylhexadecahydro-1H-cyclopenta[a]phenanthren-17-yl]butanoic acid (non-preferred name)
Description:
The chemical substance with the name "(3R)-3-[(3R,5R,8R,9S,10S,12S,13R,14S,17R)-3,12-dihydroxy-10,13-dimethylhexadecahydro-1H-cyclopenta[a]phenanthren-17-yl]butanoic acid" and CAS number "53608-86-9" is a steroid derivative characterized by a complex polycyclic structure. It features multiple chiral centers, indicating that it exists in specific stereoisomeric forms, which can significantly influence its biological activity and interactions. The presence of hydroxyl groups suggests potential for hydrogen bonding, which may enhance solubility in polar solvents and influence its reactivity. The butanoic acid moiety indicates that it has carboxylic acid functionality, which can participate in acid-base reactions and contribute to its overall acidity. This compound may exhibit various pharmacological properties, potentially acting as a hormone or hormone analog, given its structural resemblance to steroid hormones. Its intricate structure and functional groups suggest that it could interact with biological systems in specific ways, making it of interest in medicinal chemistry and pharmacology.
Formula:C23H38O4
InChI:InChI=1/C23H38O4/c1-13(10-21(26)27)17-6-7-18-16-5-4-14-11-15(24)8-9-22(14,2)19(16)12-20(25)23(17,18)3/h13-20,24-25H,4-12H2,1-3H3,(H,26,27)/t13-,14-,15-,16+,17-,18+,19+,20+,22+,23-/m1/s1
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Found 6 products.
(3α,5β,12α)-3,12-Dihydroxy-24-norcholan-23-oic acid
CAS:Formula:C23H38O4Purity:95%Color and Shape:SolidMolecular weight:378.5454Nordeoxycholic acid
CAS:<p>Nordeoxycholic acid (norDCA) is a metabolite of norcholic acid, which is associated with glucose and lipid metabolism.</p>Formula:C23H38O4Purity:98.547%Color and Shape:SolidMolecular weight:378.55Nor-Desoxycholic Acid
CAS:Controlled Product<p>Stability Hygroscopic<br>Applications A derivative of Deoxycholic acid (DC); the bile acid nor-DC showed considerable and continuing efflux into the perfusate; this involved mostly the unchanged acid. Nor-DC was not amidated but was metabolized to mostly ester glucuronides and hydroxylated derivatives.<br>References Haslewood, G., et al.: Biochem. J., 62, 637 (1956), Clayton, L. M., et al.: J. Pharmacol. Exp. Therap., 248, 1130 (1989), Aggarwal, S., et al.: Steroids, 57, 107 (1992), Batta, A., et al.: J. Lipid Res., 33, 1403 (1992),<br></p>Formula:C23H38O4Color and Shape:NeatMolecular weight:378.55Nor-desoxycholic acid
CAS:Controlled Product<p>Nor-desoxycholic acid is a bile acid derivative, which is a secondary bile acid originally derived from the microbial metabolism of primary bile acids. It is sourced from the bacterial transformation of cholic acid in the intestines. With its molecular structure altered by the removal of a hydroxyl group at a specific carbon position, Nor-desoxycholic acid plays a role in modulating cholesterol and lipid metabolism.</p>Formula:C23H38O4Purity:Min. 95%Color and Shape:White/Off-White SolidMolecular weight:378.55 g/mol





