Dehydrolithocholic acid (BioDeep_00000003938)
Bile acids
代谢物信息卡片
化学式: C24H38O3 (374.2821)
中文名称:
谱图信息:
最多检出来源 Homo sapiens(plant) 7.69%
分子结构信息
SMILES: CC(CCC(=O)O)C1CCC2C1(CCC3C2CCC4C3(CCC(=O)C4)C)C
InChI: InChI=1S/C24H38O3/c1-15(4-9-22(26)27)19-7-8-20-18-6-5-16-14-17(25)10-12-23(16,2)21(18)11-13-24(19,20)3/h15-16,18-21H,4-14H2,1-3H3,(H,26,27)
描述信息
D005765 - Gastrointestinal Agents > D001647 - Bile Acids and Salts
D005765 - Gastrointestinal Agents > D002793 - Cholic Acids
同义名列表
60 个代谢物同义名
Dehydrolithocholic acid; 3-Oxo-5α-cholan-24-oic Acid; 3-Ketocholanic acid; 3-Oxo-5beta-cholanate; (4R)-4-[(5R,8R,9S,10S,13R,14S,17R)-10,13-dimethyl-3-oxo-1,2,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-17-yl]pentanoic acid; (5-beta)-3-Oxocholan-24-oic acid; (5beta,9beta)-3-Oxocholan-24-Oic Acid; (5beta)-3-Oxo-Cholan-24-Oic Acid; 3-keto LCA; 3-keto Lithocholate; 3-keto lithocholic acid; 3-keto-5 beta-cholanoic acid; 3-KETO-5.BETA.-CHOLAN-24-OIC ACID; 3-Keto-5.beta.-cholanic acid; 3-KETO-5BETA-CHOLAN-24-OIC ACID; 3-Keto-5beta-cholanic acid; 3-keto-5beta-cholanoic acid; 3-keto-LCA; 3-keto-lithocholic acid; 3-ketocholanoic acid; 3-Ketolithocholic acid; 3-KLCA; 3-oxo LCA; 3-oxo Lithocholate; 3-oxo lithocholic acid; 3-oxo-5 beta-cholan-24-oic acid; 3-Oxo-5-beta-cholan-24-oic acid; 3-Oxo-5-cholanoic acid; 3-Oxo-5??-cholanoic acid; 3-Oxo-5.beta.-cholan-24-oic acid; 3-Oxo-5|A-cholanoic Acid; 3-Oxo-5b-cholanoic Acid; 3-Oxo-5beta-cholan-24-oic Acid; 3-oxo-5beta-cholanic acid; 3-Oxo-5beta-cholanoic Acid; 3-oxo-lithocholic acid; 3-oxocholan-24-oic acid; 3-Oxocholan-24-oic acid, (5.beta.)-; 3-Oxocholanic acid; 3-Oxolithocholic acid; 3KL; 5-beta-Cholan-24-oic acid, 3-oxo-; 5-beta-Cholanic acid-3-one; 5.beta.-Cholan-24-oic acid, 3-oxo-; 5.beta.-Cholanic acid-3-one; 5.BETA.-CHOLANIC ACID, 3-OXO-; 5BETA-CHOLAN-24-OIC ACID, 3-OXO-; 5beta-Cholanic acid-3-one; 5BETA-CHOLANIC ACID, 3-OXO-; 96JBM35FXF; Cholan-24-oic acid, 3-oxo-, (5-beta)-; Cholan-24-oic acid, 3-oxo-, (5-beta)-(9CI); Cholan-24-oic acid, 3-oxo-, (5.beta.)-; Cholan-24-oic acid, 3-oxo-, (5beta)-; Dehydrolithocholic acid; 5|A-cholanic acid-3-one; Dehydrolithocholic acid;3-oxoLCA; DHLCA; Lithocholic acid, dehydro-; UNII-96JBM35FXF; 4-(10,13-dimethyl-3-oxo-1,2,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-17-yl)pentanoic acid
数据库引用编号
17 个数据库交叉引用编号
- ChEBI: CHEBI:17639
- ChEBI: CHEBI:176828
- KEGG: C03070
- PubChem: 5283906
- PubChem: 543448
- Metlin: METLIN42717
- ChEMBL: CHEMBL410893
- CAS: 1553-56-6
- PMhub: MS000013737
- PubChem: 5970
- LipidMAPS: LMST04010127
- PDB-CCD: 3KL
- 3DMET: B01628
- NIKKAJI: J39.835G
- RefMet: Dehydrolithocholic acid
- KNApSAcK: 17639
- MeSH: 3-oxocholan-24-oic acid
分类词条
相关代谢途径
Reactome()
BioCyc()
PlantCyc()
代谢反应
个相关的代谢反应过程信息。
Reactome()
BioCyc()
WikiPathways()
Plant Reactome()
INOH()
PlantCyc()
COVID-19 Disease Map()
PathBank()
PharmGKB()
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
- Satoshi Endo, Namiki Miyagi, Toshiyuki Matsunaga, Akira Ikari. Rabbit dehydrogenase/reductase SDR family member 11 (DHRS11): Its identity with acetohexamide reductase with broad substrate specificity and inhibitor sensitivity, different from human DHRS11.
Chemico-biological interactions.
2019 May; 305(?):12-20. doi:
10.1016/j.cbi.2019.03.026. [PMID: 30926317] - Anand K Deo, Stelvio M Bandiera. Biotransformation of lithocholic acid by rat hepatic microsomes: metabolite analysis by liquid chromatography/mass spectrometry.
Drug metabolism and disposition: the biological fate of chemicals.
2008 Feb; 36(2):442-51. doi:
10.1124/dmd.107.017533. [PMID: 18039809] - Ryutaro Adachi, Yoshio Honma, Hiroyuki Masuno, Katsuyoshi Kawana, Iichiro Shimomura, Sachiko Yamada, Makoto Makishima. Selective activation of vitamin D receptor by lithocholic acid acetate, a bile acid derivative.
Journal of lipid research.
2005 Jan; 46(1):46-57. doi:
10.1194/jlr.m400294-jlr200. [PMID: 15489543] - R W Owen, R F Bilton. Metabolism of unsaturated bile acids and androstanes by human faecal bacteria.
Journal of steroid biochemistry.
1985 Jun; 22(6):817-22. doi:
10.1016/0022-4731(85)90291-2. [PMID: 4021485]
