(3a,5b,7a,12a)-3,7,12-trihydroxy-Cholestan-26-oic acid

(3a,5b,7a,12a)-3,7,12-trihydroxy-Cholestan-26-oic acid
  • CAS No.:547-98-8

Important Notice

  1. This product is a chemical product/pharmaceutical intermediate. It is not a drug, an active pharmaceutical ingredient (API), or a pharmaceutical-grade material. It has not been granted a drug approval number or a Chemical Drug Substance Approval Notice, has not passed drug-related review and approval, and is not manufactured, tested, or released in accordance with pharmaceutical GMP.
  2. This product is intended solely for non-clinical research, process development, quality studies, further chemical processing, or chemical synthesis. It must not be used in drug-product manufacturing, clinical trials, clinical diagnosis, or administration to humans or animals, or be sold, used as an input, submitted for regulatory filing, or released as an API or pharmaceutical material.
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(3a,5b,7a,12a)-3,7,12-trihydroxy-Cholestan-26-oic acid Basic information
Product Name:(3a,5b,7a,12a)-3,7,12-trihydroxy-Cholestan-26-oic acid
Synonyms:(3a,5b,7a,12a)-3,7,12-trihydroxy-Cholestan-26-oic acid;3α,7α,12α-Trihydroxy-5β-cholestan-26-oic acid;3α,7α,12α-Trihydroxy-5β-cholestan-27-oic acid;3α,7α,12α-Trihydroxy-5β-cholestanoic acid;3α,7α,12α-Trihydroxycoprostanoic acid;THCA;Trihydroxycholestanoic acid;3alpha,7alpha,12alpha-trihydroxy-5beta-cholestan-26-oic acid
CAS:547-98-8
MF:C27H46O5
MW:450.65
EINECS:
Product Categories:
Mol File:547-98-8.mol
(3a,5b,7a,12a)-3,7,12-trihydroxy-Cholestan-26-oic acid Chemical Properties
storage temp. -20°C
solubility Chloroform (Slightly, Heated), DMSO (Slightly), Ethanol (Slightly), Methanol (Sl
form Solid
color White to Off-White
Safety Information
MSDS Information
(3a,5b,7a,12a)-3,7,12-trihydroxy-Cholestan-26-oic acid Usage And Synthesis
Uses3α,7α,12α-Trihydroxycoprostanic Acid is a precursor of Cholic Acid (C432600), it undergoes side chain oxidation during the synthesis of bile acids. It was found that Zellweger’s syndrome patients have abnormal mitochondrial structure, the organelle that is responsible for the side chain oxidation, and as a consequence, excess amounts of 3α,7α,12α-Trihydroxycoprostanic Acid.
DefinitionChEBI: A steroid acid that is 5beta-cholestan-26-oic acid which is substituted by hydroxy groups as the 3alpha, 7alpha, and 12alpha positions.
General DescriptionTrihydroxycholestanoic acid (THCA) is an oxidative metabolite of cholesterol and a precursor to bile acids. Very long-chain acyl-CoA synthetase (VLCS) associated with endoplasmic reticulum and peroxisomes activates THCA, the C27 bile acid intermediate.
Biochem/physiol ActionsTrihydroxycholestanoic acid (THCA) and dihydroxycholestanoic (DHCA) accumulation is observed in Zellweger syndrome and cholestatic liver disease. The synthesis of (25R)-isomer of DHCA and THCA is favored by mitochondrial 27-hydroxylase.
(3a,5b,7a,12a)-3,7,12-trihydroxy-Cholestan-26-oic acid Preparation Products And Raw materials

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