Epi-coprostanol (BioDeep_00000003825)

Main id: BioDeep_00000018885

 

human metabolite Endogenous


代谢物信息卡片


(1S,2S,5R,7S,10R,11S,14R,15R)-2,15-dimethyl-14-[(2R)-6-methylheptan-2-yl]tetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadecan-5-ol

化学式: C27H48O (388.37049579999996)
中文名称:
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: C1[C@]2(C)[C@@]3([H])CC[C@]4(C)[C@@]([H])([C@]([H])(C)CCCC(C)C)CC[C@@]4([H])[C@]3([H])CC[C@@]2([H])C[C@H](O)C1
InChI: InChI=1S/C27H48O/c1-18(2)7-6-8-19(3)23-11-12-24-22-10-9-20-17-21(28)13-15-26(20,4)25(22)14-16-27(23,24)5/h18-25,28H,6-17H2,1-5H3/t19-,20+,21-,22+,23-,24+,25+,26+,27-/m1/s1

描述信息

Epi-coprostanol, also known as epicholestanol or presteron, belongs to the class of organic compounds known as cholesterols and derivatives. Cholesterols and derivatives are compounds containing a 3-hydroxylated cholestane core. Thus, epi-coprostanol is considered to be a sterol lipid molecule. Epi-coprostanol is a very hydrophobic molecule, practically insoluble in water, and relatively neutral.
Epi-coprostanol is a 27 carbon stanol formed from the biohydrogenation of cholesterol (cholest-5en-3β-ol) in the gut of most higher animals and birds. It is a breakdown product of 5b-coprastanol and can be found in treated sewage. It is considered to be an antioxidant and is a major constituent of ambergris. [HMDB]
Same as: D01527

同义名列表

30 个代谢物同义名

(1S,2S,5R,7S,10R,11S,14R,15R)-2,15-dimethyl-14-[(2R)-6-methylheptan-2-yl]tetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadecan-5-ol; (3-alpha,5-alpha)-Cholestan-3-ol; 3alpha-Hydroxy-5alpha-cholestane; 5alpha-cholestan-3alpha-ol; 5beta-Cholestane-3alpha-ol; 5beta-Cholestan-3alpha-ol; 3a-Hydroxy-5a-cholestane; (3-Α,5-α)-cholestan-3-ol; 3Α-hydroxy-5α-cholestane; (3-a,5-a)-Cholestan-3-ol; cholestan-3α-ol; Epidehydrocholesterin; Epidihydrocholesterin; 5b-Cholestane-3a-ol; 5a-Cholestan-3a-ol; 5Α-cholestan-3α-ol; 5b-Cholestan-3a-ol; alpha-Coprostanol; 5beta-Cholestanol; Epi-coprostanol; Epi-coprosterol; Epi-cholestanol; Epicoprosterol; Epicoprostanol; Epicholestanol; 5b-cholestanol; a-Coprostanol; ST 27:0;O; Presteron; Dihydrin



数据库引用编号

13 个数据库交叉引用编号

分类词条

相关代谢途径

Reactome(0)

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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)

3 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

  • Matthew G K Benesch, David A Mannock, Ronald N McElhaney. Sterol chemical configuration influences the thermotropic phase behaviour of dipalmitoylphosphatidylcholine bilayers containing 5α-cholestan-3β- and 3α-ol. Chemistry and physics of lipids. 2011 Jan; 164(1):62-9. doi: 10.1016/j.chemphyslip.2010.10.003. [PMID: 21055394]
  • Jingming Wu, Ruikang Hu, Junqi Yue, Zhaoguang Yang, Lifeng Zhang. Determination of fecal sterols by gas chromatography-mass spectrometry with solid-phase extraction and injection-port derivatization. Journal of chromatography. A. 2009 Feb; 1216(7):1053-8. doi: 10.1016/j.chroma.2008.12.054. [PMID: 19147150]