CAS 10538-59-7
:7-ketolithocholic Methyl ester
Description:
7-Ketolithocholic methyl ester is a bile acid derivative that belongs to the class of steroid compounds. It is characterized by its structural features, which include a steroid nucleus with a ketone group at the 7-position and a methyl ester functional group. This compound is typically derived from lithocholic acid, a bile acid that plays a role in the emulsification and absorption of dietary fats. The presence of the methyl ester group enhances its lipophilicity, which can influence its biological activity and solubility properties. 7-Ketolithocholic methyl ester may exhibit various physiological effects, including potential roles in lipid metabolism and signaling pathways. Its chemical properties, such as melting point, solubility, and reactivity, are influenced by its steroidal structure and functional groups. As with many bile acid derivatives, it may also have implications in pharmacology and toxicology, warranting further investigation into its biological effects and potential therapeutic applications.
Formula:C25H40O4
InChI:InChI=1S/C25H40O4/c1-15(5-8-22(28)29-4)18-6-7-19-23-20(10-12-25(18,19)3)24(2)11-9-17(26)13-16(24)14-21(23)27/h15-20,23,26H,5-14H2,1-4H3/t15-,16+,17-,18-,19+,20+,23+,24+,25-/m1/s1
InChI key:InChIKey=FNBYYFMYNRYPPC-YLOOLPOOSA-N
SMILES:C[C@@]12[C@]([C@]3([C@@]([C@]4(C)[C@](CC3=O)(C[C@H](O)CC4)[H])(CC1)[H])[H])(CC[C@@]2([C@@H](CCC(OC)=O)C)[H])[H]
Synonyms:- 3α-Hydroxy-7-oxo-5β-cholan-24-oic acid methyl ester
- 5β-Cholan-24-oic acid, 3α-hydroxy-7-oxo-, methyl ester
- 5β-Cholanic acid, 3α-hydroxy-7-oxo-, methyl ester
- 7-Ketolithocholic acid methyl ester
- Cholan-24-oic acid, 3-hydroxy-7-oxo-, methyl ester, (3α,5β)-
- Methyl (3α,5β)-3-hydroxy-7-oxocholan-24-oate
- Methyl 3α-hydroxy-7-keto-5β-cholanate
- Methyl 3α-hydroxy-7-oxo-5β-cholan-24-oate
- Methyl 3α-hydroxy-7-oxo-5β-cholanoate
- Methyl 7-keto-3alpha-hydroxy-5beta-cholanoate
- Methyl 7-keto-3α-hydroxy-5β-cholanoate
- See more synonyms
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Found 8 products.
(R)-Methyl 4-((3R,5S,8R,9S,10S,13R,14S,17R)-3-hydroxy-10,13-dimethyl-7-oxohexadecahydro-1H-cyclopenta[a]phenanthren-17-yl)pentanoate
CAS:Formula:C25H40O4Purity:95%Color and Shape:SolidMolecular weight:404.5827Nutriacholic Acid Methyl Ester
CAS:Controlled ProductFormula:C25H40O4Color and Shape:NeatMolecular weight:404.58Methyl 7-keto-3a-hydroxy-5b-cholanoate
CAS:Controlled ProductMethyl 7-keto-3a-hydroxy-5b-cholanoate is a cholic acid derivative that has been shown to reduce intestinal cholesterol absorption. It is also used in the treatment of genetic disorders such as familial hypercholesterolemia. Ursodeoxycholic acid, which is a naturally occurring bile acid, is produced from methyl 7-keto-3a-hydroxy-5b-cholanoate by the action of bacteria in the human colon. This conversion process can be accelerated by adding ursodeoxycholic acid to the diet. Methyl 7-keto-3a-hydroxy-5b-cholanoate has also been shown to increase fecal bile acids and fecal sterols, which are important for maintaining normal bowel function and reducing cholesterol levels in the blood. Methyl 7--keto--3a--hydroxy--5b--cholanoate may be used as aFormula:C25H40O4Purity:Min. 95%Molecular weight:404.58 g/mol(R)-Methyl 4-((3R,5S,8R,9S,10S,13R,14S,17R)-3-hydroxy-10,13-dimethyl-7-oxohexadecahydro-1H-cyclopenta[a]phenanthren-17-yl)pentanoate
CAS:(R)-Methyl 4-((3R,5S,8R,9S,10S,13R,14S,17R)-3-hydroxy-10,13-dimethyl-7-oxohexadecahydro-1H-cyclopenta[a]phenanthren-17-yl)pentanoate is a useful organic compound for research related to life sciences. The catalog number is T66656 and the CAS number is 10538-59-7.Formula:C25H40O4Color and Shape:SolidMolecular weight:404.591
