2-Methoxyestrone 3-glucuronide (BioDeep_00000008512)

 

Secondary id: BioDeep_00000638222

human metabolite Endogenous blood metabolite Volatile Flavor Compounds


代谢物信息卡片


3,4,5-trihydroxy-6-{[(1S,10R,11S,15S)-4-methoxy-15-methyl-14-oxotetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadeca-2,4,6-trien-5-yl]oxy}oxane-2-carboxylic acid

化学式: C25H32O9 (476.2046222)
中文名称:
谱图信息: 最多检出来源 Homo sapiens(feces) 8.99%

分子结构信息

SMILES: CC12CCC3C(C1CCC2=O)CCC4=CC(=C(C=C34)OC)OC5C(C(C(C(O5)C(=O)O)O)O)O
InChI: InChI=1S/C25H32O9/c1-25-8-7-12-13(15(25)5-6-18(25)26)4-3-11-9-17(16(32-2)10-14(11)12)33-24-21(29)19(27)20(28)22(34-24)23(30)31/h9-10,12-13,15,19-22,24,27-29H,3-8H2,1-2H3,(H,30,31)/t12-,13+,15-,19-,20-,21+,22-,24+,25-/m0/s1

描述信息

2-Methoxyestrone 3-glucuronide belongs to the class of organic compounds known as steroid glucuronide conjugates. These are sterol lipids containing a glucuronide moiety linked to the steroid skeleton. Thus, 2-methoxyestrone 3-glucuronide is considered to be a steroid conjugate lipid molecule. 2-Methoxyestrone 3-glucuronide is a very hydrophobic molecule, practically insoluble (in water), and relatively neutral. 2-Methoxyestrone 3-glucuronide is a natural human metabolite of 2-methoxyestrone generated in the liver by UDP glucuronosyltransferase. 2-Methoxyestrone is a metabolite of 2-hydroxyestrone (a nonuterotrophic metabolite of estradiol). Glucuronidation is used to assist in the excretion of toxic substances, drugs, or other substances that cannot be used as an energy source. Glucuronic acid is attached via a glycosidic bond to the substance, and the resulting glucuronide, which has a much higher water solubility than the original substance, is eventually excreted by the kidneys.
2-Methoxyestrone 3-glucuronide is a natural human metabolite of 2-Methoxyestrone generated in the liver by UDP glucuonyltransferase. A glucuronide conjugate of 2-methodxyestrone formed by UDP-glucuronylstransferase (UTP). 2-methoxyestrone is a metabolite of 2-hydroxyestrone (a nonuterotrophic metabolite of estradiol)
D006730 - Hormones, Hormone Substitutes, and Hormone Antagonists > D006728 - Hormones

同义名列表

24 个代谢物同义名

3,4,5-trihydroxy-6-{[(1S,10R,11S,15S)-4-methoxy-15-methyl-14-oxotetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadeca-2,4,6-trien-5-yl]oxy}oxane-2-carboxylic acid; 2-methoxy,3-hydroxy-estra-1,3,5(10)-trien-17-one 3-D-glucuronide; 2-Methoxyestrone 3-O-(beta-D-glucuronic acid); 2-Methoxyestrone 3-O-(β-D-glucuronic acid); 2-Methoxyestrone 3-O-(b-D-glucuronic acid); 2-Methoxyestrone 3-O-(beta-D-glucuronate); 2-Methoxyestrone 3-O-(β-D-glucuronate); 2-Methoxyestrone 3-O-(b-D-glucuronate); 2-Methoxyestrone 3-glucosiduronic acid; 2-Methoxyestrone 3-beta-D-glucuronide; 2-Methoxyestrone 3-beta-glucuronide; 2-Methoxyestrone 3-glucosiduronate; 2-Methoxyestrone 3-b-D-glucuronide; 2-Methoxyestrone 3-β-D-glucuronide; 2-Methoxyestrone glucosiduronate; 2-Methoxyestrone 3-glucuronoside; 2-Methoxyestrone 3-O-glucuronide; 2-Methoxyestrone 3-β-glucuronide; 2-Methoxyestrone 3-b-glucuronide; 2-Methoxyestrone 3-glucuronide; 2-Methoxyestrone-3-glucuronide; ST 19:4;O3;GlcA; 2-MeOE1 3g; 2-Methoxyestrone 3-glucuronide



数据库引用编号

16 个数据库交叉引用编号

分类词条

相关代谢途径

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代谢反应

2 个相关的代谢反应过程信息。

Reactome(0)

BioCyc(0)

WikiPathways(2)

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

  • Delwyn G Cooke, Leonard F Blackwell. Clearing of suspensions of Micrococcus lysodeikticus catalysed by lysozymes from hen, goose, and turkey egg whites, human milk, and phage T4. Assessment of potential as signal generators for homogeneous enzyme immunoassays for urinary steroids. Journal of immunoassay & immunochemistry. 2007; 28(2):67-90. doi: 10.1080/15321810701209704. [PMID: 17424827]