β-Muricholic acid (BioDeep_00000014338)
human metabolite PANOMIX_OTCML-2023 Endogenous Bile acids PANOMIX LipidSearch
代谢物信息卡片
化学式: C24H40O5 (408.28755900000004)
中文名称: β-鼠胆酸
谱图信息:
最多检出来源 Homo sapiens(feces) 0.14%
Last reviewed on 2024-09-13.
Cite this Page
β-Muricholic acid. BioDeep Database v3. PANOMIX ltd, a top metabolomics service provider from China.
https://query.biodeep.cn/s/β-muricholic_acid (retrieved
2024-11-05) (BioDeep RN: BioDeep_00000014338). Licensed
under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).
分子结构信息
SMILES: CC(CCC(=O)O)C1CCC2C1(CCC3C2C(C(C4C3(CCC(C4)O)C)O)O)C
InChI: InChI=1S/C24H40O5/c1-13(4-7-19(26)27)15-5-6-16-20-17(9-11-23(15,16)2)24(3)10-8-14(25)12-18(24)21(28)22(20)29/h13-18,20-22,25,28-29H,4-12H2,1-3H3,(H,26,27)/t13-,14-,15-,16+,17+,18+,20+,21+,22-,23-,24-/m1/s1
描述信息
3a,6b,7b-Trihydroxy-5b-cholanoic acid, also known as beta-muricholic acid, is a bile acid. 3a,6b,7b-Trihydroxy-5b-cholanoic acid belongs to the class of compounds known muricholic acids in which the hydroxy groups at positions 6 and 7 both have a beta configuration. It is also classified as a 6beta-hydroxy steroid, a 7beta-hydroxy steroid, a steroid acid and a bile acid. Muricholic acids are a group of bile acids that are particularly abundant in mice, which gives them their name. Muricholic acids are also found at low concentrations in other mammalian species, including humans (PMID: 12543708). Muricholic acids differ from the primary bile acids found in humans (which are cholic acid and chenodeoxycholic acid) by having a hydroxyl group in the beta-conformation at the 6-position. The orientation of the hydroxyl group at the 7 position defines alpha- or beta-muricholic acid. Muricholic acids are detectable at low concentrations in human urine (PMIDL 1629271). The enzyme responsible for the 6-hydroxylation reactions forming muricholates in rodents is the cytochrome P450 Cyp2c70. This produces alpha-muricholic acid from chenodeoxycholic acid, and beta-muricholic acid from ursodeoxycholic acid. Bile acids, such as muricholic acid, are steroid acids found predominantly in the bile of mammals. The distinction between different bile acids is minute, depending only on the presence or absence of hydroxyl groups on positions 3, 6, 7, and 12. Bile acids are physiological detergents that facilitate excretion, absorption, and transport of fats and sterols in the intestine and liver. Bile acids are also steroidal amphipathic molecules derived from the catabolism of cholesterol. They modulate bile flow and lipid secretion, are essential for the absorption of dietary fats and vitamins, and have been implicated in the regulation of all the key enzymes involved in cholesterol homeostasis. Bile acids recirculate through the liver, bile ducts, small intestine and portal vein to form an enterohepatic circuit. They exist as anions at physiological pH and, consequently, require a carrier for transport across the membranes of the enterohepatic tissues. The unique detergent properties of bile acids are essential for the digestion and intestinal absorption of hydrophobic nutrients. Bile acids have potent toxic properties (e.g. membrane disruption) and there are a plethora of mechanisms to limit their accumulation in blood and tissues (PMID: 11316487, 16037564, 12576301, 11907135).
3a,6b,7b-Trihydroxy-5b-cholanoic acid is a bile acid found in urine exhibiting a complex modification pattern, including free, glyco- and sulfoconjugated forms (PMID 3834660).
β-Muricholic acid is a potent and orally active biliary cholesterol-desaturating agent. β-Muricholic acid prevents cholesterol gallstones. β-Muricholic acid inhibits lipid accumulation. β-Muricholic acid has the potential for the research of nonalcoholic fatty liver disease (NAFLD)[1][2].
同义名列表
53 个代谢物同义名
(4R)-4-[(1S,2R,5R,7R,8S,9R,10S,11S,14R,15R)-5,8,9-trihydroxy-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadecan-14-yl]pentanoic acid; 3α,6β,7β-Trihydroxy-5β-cholan-24-oic Acid; (3alpha,5beta,6beta,7beta)-3,6,7-Trihydroxycholan-24-Oic acid; (3alpha,5beta,6beta,7beta)-3,6,7-Trihydroxycholan-24-Oate; 3 alpha,6 alpha,7 beta-Trihydroxy-5 beta-cholanoic acid; 3alpha,6beta,7beta-Trihydroxy-5beta-cholan-24-oic Acid; Muricholic acid, (3alpha,5alpha,6alpha,7alpha)-isomer; Muricholic acid, (3alpha,5beta,6alpha,7alpha)-isomer; Muricholic acid, (3alpha,5beta,6alpha,7beta)-isomer; Muricholic acid, (3alpha,5beta,6beta,7alpha)-isomer; 3alpha,6beta,7beta-Trihydroxy-5beta-cholan-24-Oate; Muricholic acid, (3alpha,5beta,6beta,7beta)-isomer; (3Α,5β,6β,7β)-3,6,7-trihydroxycholan-24-Oic acid; (3a,5b,6b,7b)-3,6,7-Trihydroxycholan-24-Oic acid; (3a,5b,6b,7b)-3,6,7-Trihydroxycholan-24-Oate; (3Α,5β,6β,7β)-3,6,7-trihydroxycholan-24-Oate; 5beta-Cholanic acid-3alpha,6beta,7beta-triol; 3a,6b,7b-Trihydroxy-5b-cholan-24-Oic acid; 3,6,7-Trihydroxy-5beta-cholan-24-Oic acid; 3Α,6β,7β-trihydroxy-5β-cholan-24-Oic acid; 5beta-Cholanate-3alpha,6beta,7beta-triol; 3,6,7-Trihydroxy-5b-cholan-24-Oic acid; 3,6,7-Trihydroxy-5β-cholan-24-Oic acid; 3,6,7-Trihydroxy-5beta-cholan-24-Oate; 3a,6b,7b-Trihydroxy-5b-cholanoic acid; 3Α,6β,7β-trihydroxy-5β-cholan-24-Oate; 3a,6b,7b-Trihydroxy-5b-cholan-24-Oate; 3a,6b,7b-Trihydroxy-5b-cholanic acid; 3,6,7-Trihydroxy-5b-cholan-24-Oate; 3,6,7-Trihydroxy-5β-cholan-24-Oate; 3a,6b,7b-Trihydroxy-5b-cholanoate; Trihydroxy-5 alpha-cholanoic acid; 3,6,7-Trihydroxy-5-cholanoic acid; 3a,6b,7b-Trihydroxy-5b-cholanate; 5b-Cholanic acid-3a,6b,7b-triol; 5Β-cholanic acid-3α,6β,7β-triol; Muricholic acid, sodium salt; 5b-Cholanate-3a,6b,7b-triol; 5Β-cholanate-3α,6β,7β-triol; omega-muricholic acid; alpha-muricholic acid; beta-muricholic acid; b-Muricholic acid; Β-muricholic acid; beta-Muricholate; Muricholic acid; Hyocholic Acid; Β-muricholate; b-Muricholate; beta-MCA; b-MCA; Β-mca; Beta-Muricholic acid (β-MCA)
数据库引用编号
14 个数据库交叉引用编号
- ChEBI: CHEBI:81298
- KEGG: C17726
- PubChem: 5283853
- HMDB: HMDB0000415
- Metlin: METLIN42670
- MetaCyc: CPD-16583
- foodb: FDB022031
- chemspider: 4446941
- CAS: 2393-59-1
- ChEBI: CHEBI:134119
- LipidMAPS: LMST04010067
- NIKKAJI: J367.450I
- PANOMIX LipidSearch: CA-19
- medchemexpress: HY-133707
分类词条
相关代谢途径
Reactome(0)
BioCyc(0)
PlantCyc(0)
代谢反应
0 个相关的代谢反应过程信息。
Reactome(0)
BioCyc(0)
WikiPathways(0)
Plant Reactome(0)
INOH(0)
PlantCyc(0)
COVID-19 Disease Map(0)
PathBank(0)
PharmGKB(0)
2 个相关的物种来源信息
在这里通过桑基图来展示出与当前的这个代谢物在我们的BioDeep知识库中具有相关联信息的其他代谢物。在这里进行关联的信息来源主要有:
- PubMed: 来源于PubMed文献库中的文献信息,我们通过自然语言数据挖掘得到的在同一篇文献中被同时提及的相关代谢物列表,这个列表按照代谢物同时出现的文献数量降序排序,取前10个代谢物作为相关研究中关联性很高的代谢物集合展示在桑基图中。
- NCBI Taxonomy: 通过文献数据挖掘,得到的代谢物物种来源信息关联。这个关联信息同样按照出现的次数降序排序,取前10个代谢物作为高关联度的代谢物集合展示在桑吉图上。
- Chemical Taxonomy: 在物质分类上处于同一个分类集合中的其他代谢物
- Chemical Reaction: 在化学反应过程中,存在为当前代谢物相关联的生化反应过程中的反应底物或者反应产物的关联代谢物信息。
点击图上的相关代谢物的名称,可以跳转到相关代谢物的信息页面。
文献列表
- Zeping Zhang, Boyan Zhang, Xianzhe Jiang, Yue Yu, Yimeng Cui, Hailing Luo, Bing Wang. Hyocholic acid retards renal fibrosis by regulating lipid metabolism and inflammatory response in a sheep model.
International immunopharmacology.
2023 Jul; 122(?):110670. doi:
10.1016/j.intimp.2023.110670
. [PMID: 37481851] - Yang Xie, Feng Shen, Yafang He, Canjie Guo, Ruixu Yang, Haixia Cao, Qin Pan, Jiangao Fan. Gamma-Muricholic Acid Inhibits Nonalcoholic Steatohepatitis: Abolishment of Steatosis-Dependent Peroxidative Impairment by FXR/SHP/LXRα/FASN Signaling.
Nutrients.
2023 Mar; 15(5):. doi:
10.3390/nu15051255
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Hepatology communications.
2022 12; 6(12):3363-3378. doi:
10.1002/hep4.2099
. [PMID: 36196594] - Antwi-Boasiako Oteng, Sei Higuchi, Alexander S Banks, Rebecca A Haeusler. Cyp2c-deficiency depletes muricholic acids and protects against high-fat diet-induced obesity in male mice but promotes liver damage.
Molecular metabolism.
2021 11; 53(?):101326. doi:
10.1016/j.molmet.2021.101326
. [PMID: 34438105] - Dany Gaillard, David Masson, Erwan Garo, Maamar Souidi, Jean-Paul Pais de Barros, Kristina Schoonjans, Jacques Grober, Philippe Besnard, Charles Thomas. Muricholic Acids Promote Resistance to Hypercholesterolemia in Cholesterol-Fed Mice.
International journal of molecular sciences.
2021 Jul; 22(13):. doi:
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. [PMID: 34281217] - Anders Ø Petersen, Hanna Julienne, Tuulia Hyötyläinen, Partho Sen, Yong Fan, Helle Krogh Pedersen, Sirkku Jäntti, Tue H Hansen, Trine Nielsen, Torben Jørgensen, Torben Hansen, Pernille Neve Myers, H Bjørn Nielsen, S Dusko Ehrlich, Matej Orešič, Oluf Pedersen. Conjugated C-6 hydroxylated bile acids in serum relate to human metabolic health and gut Clostridia species.
Scientific reports.
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Cell metabolism.
2021 04; 33(4):791-803.e7. doi:
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PloS one.
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