CAS 2464-18-8
:Allocholic acid
Description:
Allocholic acid, with the CAS number 2464-18-8, is a bile acid that is derived from cholesterol and plays a significant role in the digestion and absorption of dietary fats. It is characterized by its steroid structure, which includes a hydroxyl group and a carboxylic acid group, contributing to its amphipathic nature. This property allows it to interact with both lipophilic and hydrophilic substances, facilitating the emulsification of fats in the gastrointestinal tract. Allocholic acid is primarily found in the bile of certain animals and is involved in the enterohepatic circulation, where it is reabsorbed and recycled. Its biological functions extend beyond digestion, as it may also influence cholesterol metabolism and gut microbiota composition. Additionally, allocholic acid can exhibit various physiological effects, including potential roles in signaling pathways. Its study is important in understanding metabolic disorders and the pharmacological applications of bile acids.
Formula:C24H40O5
InChI:InChI=1S/C24H40O5/c1-13(4-7-21(28)29)16-5-6-17-22-18(12-20(27)24(16,17)3)23(2)9-8-15(25)10-14(23)11-19(22)26/h13-20,22,25-27H,4-12H2,1-3H3,(H,28,29)/t13-,14-,15-,16-,17+,18+,19-,20+,22+,23+,24-/m1/s1
InChI key:InChIKey=BHQCQFFYRZLCQQ-PGHAKIONSA-N
SMILES:O[C@H]1[C@]2([C@]3([C@@](C)([C@@]([C@@H](CCC(O)=O)C)(CC3)[H])[C@@H](O)C[C@@]2([C@]4(C)[C@@](C1)(C[C@H](O)CC4)[H])[H])[H])[H]
Synonyms:- (3Alpha,5Alpha,7Alpha,12Alpha)-3,7,12-Trihydroxycholan-24-Oic Acid
- (3α,5α,7α,12α)-3,7,12-Trihydroxycholan-24-oic acid
- 3alpha,7alpha,12alpha-Trihydroxy-5alpha-cholan-24-oic acid
- 3α,7α,12α-Trihydroxy-5α-cholanoic acid
- 5α-Allocholic acid
- 5α-Cholan-24-oic acid, 3α,7α,12α-trihydroxy-
- 5α-Cholanic acid, 3α,7α,12α-trihydroxy-
- 5α-Cholic acid
- Cholan-24-oic acid, 3,7,12-trihydroxy-, (3alpha,5alpha,7alpha,12alpha)-
- Cholan-24-oic acid, 3,7,12-trihydroxy-, (3α,5α,7α,12α)-
- Nplc 0115
- See more synonyms
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Found 8 products.
Cholan-24-oic acid, 3,7,12-trihydroxy-, (3α,5α,7α,12α)-
CAS:Formula:C24H40O5Purity:98%Color and Shape:SolidMolecular weight:408.5714Allocholic acid
CAS:<p>Allocholic acid from Carpiodes carpio bile is an olfactory stimulant & lamprey migratory pheromone.</p>Formula:C24H40O5Purity:97.2% - 99.54%Color and Shape:SolidMolecular weight:408.57Allocholic Acid
CAS:Controlled Product<p>Applications Has wide-spread occurrence in a number of sources, including man as a major biliary metabolite.<br>References Karavolas, H.J., et al.: J. Biol. Chem., 240, 1568 (1965), Tammer, A.R.: Biochem. J., 98, 25 (1966), Eneroth, P., et al.: J. Lipid Res., 7, 524 (1966), Sorensen, P.W., et al.: J. Gen. Physiol., 105, 569 (1995)<br></p>Formula:C24H40O5Color and Shape:White To Off-WhiteMolecular weight:408.57Ref: 10-F979169
5mgTo inquire10mgTo inquire25mgTo inquire50mgTo inquire100mgTo inquire250mgTo inquireAllocholic acid
CAS:Controlled Product<p>Allocholic acid is a hydroxylated derivative of allo-inositol. It has been shown to inhibit the formation of peptide hormones and is used in the treatment of cerebrotendinous xanthomatosis. Allocholic acid also inhibits molecules that inhibit enzymes, such as phosphodiesterase and lipase, which are involved in the breakdown of fat. The biological sample preparation methods have been optimized for the extraction of allocholic acid from human feces. The optimum pH for allocholic acid is 4.5-5.0. Allocholic acid can be used to inhibit prostate cancer cells and rat liver microsomes, which are important for the metabolism of fatty acids in the body. The magnesium salt form is more soluble than other salts, making it easier to use in solution form.</p>Formula:C24H40O5Purity:Min. 90 Area-%Color and Shape:White Off-White PowderMolecular weight:408.57 g/mol
