17-Epiestriol (BioDeep_00000027547)

   

human metabolite Endogenous


代谢物信息卡片


(8R,9S,13S,14S,16R,17S)-13-Methyl-7,8,9,11,12,13,14,15,16,17-decahydro-6H-cyclopenta[a]phenanthrene-3,16,17-triol

  化学式: C18H24O3 (288.1725)
中文名称: 17-环雌三醇
  谱图信息: 最多检出来源 Homo sapiens(not specific) 8.11%

分子结构信息

SMILES: CC12CCC3C(C1CC(C2O)O)CCC4=C3C=CC(=C4)O
InChI: InChI=1S/C18H24O3/c1-18-7-6-13-12-5-3-11(19)8-10(12)2-4-14(13)15(18)9-16(20)17(18)21/h3,5,8,13-17,19-21H,2,4,6-7,9H2,1H3/t13?,14?,15?,16-,17-,18+/m1/s1


描述信息

17-Epiestriol, also known as 17alpha-estriol, belongs to the class of organic compounds known as estrogens and derivatives. These are steroids with a structure containing a 3-hydroxylated estrane. Thus, 17-epiestriol is considered to be a steroid lipid molecule. 17-Epiestriol is a hydroxylated metabolite of estradiol or estrone that has a hydroxyl group at the C3-beta, 16-alpha, and 17-beta positions. Estriol is a major urinary estrogen. During pregnancy, a large amount of estriol is produced by the placenta. Isomers with inversion of the hydroxyl group or groups are called epiestriol.
A hydroxylated metabolite of estradiol or estrone that has a hydroxyl group at C3-beta, 16-alpha, and 17-beta position. Estriol is a major urinary estrogen. During pregnancy, large amount of estriol is produced by the placenta. Isomers with inversion of the hydroxyl group or groups are called epiestriol. [HMDB]

同义名列表

29 个代谢物同义名

(8R,9S,13S,14S,16R,17S)-13-Methyl-7,8,9,11,12,13,14,15,16,17-decahydro-6H-cyclopenta[a]phenanthrene-3,16,17-triol; (1S,10R,11S,13R,14S,15S)-15-methyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadeca-2,4,6-triene-5,13,14-triol; (16alpha,17alpha)-Estra-1(10),2,4-triene-3,16,17-triol; (16alpha,17alpha)-Estra-1,3,5(10)-triene-3,16,17-triol; 3,16alpha,17alpha-Trihydroxy-1,3,5(10)-estratriene; (16Α,17α)-estra-1,3,5(10)-triene-3,16,17-triol; (16Α,17α)-estra-1(10),2,4-triene-3,16,17-triol; (16a,17a)-Estra-1(10),2,4-triene-3,16,17-triol; Estra-1,3,5(10)-triene-3,16alpha,17alpha-triol; (16a,17a)-Estra-1,3,5(10)-triene-3,16,17-triol; 1,3,5(10)-Estratriene-3,16alpha,17alpha-triol; 3,16Α,17α-trihydroxy-1,3,5(10)-estratriene; 3,16a,17a-Trihydroxy-1,3,5(10)-estratriene; Estra-1,3,5(10)-triene-3,16α,17α-triol; 1,3,5(10)-Estratriene-3,16a,17a-triol; 1,3,5(10)-Estratriene-3,16α,17α-triol; 16alpha-Hydroxy-17alpha-estradiol; 16Α-hydroxy-17α-estradiol; 16a-Hydroxy-17a-estradiol; 16alpha,17alpha-Estriol; 17alpha-Epiestriol; 16a,17a-Estriol; 16Α,17α-estriol; 17alpha-Estriol; 17-Epi-estriol; 17Α-epiestriol; 17-Epiestriol; 17a-Estriol; 17Α-estriol



数据库引用编号

9 个数据库交叉引用编号

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)

1 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。

亚细胞结构定位 关联基因列表


文献列表

  • A Heather Eliassen, Donna Spiegelman, Xia Xu, Larry K Keefer, Timothy D Veenstra, Robert L Barbieri, Walter C Willett, Susan E Hankinson, Regina G Ziegler. Urinary estrogens and estrogen metabolites and subsequent risk of breast cancer among premenopausal women. Cancer research. 2012 Feb; 72(3):696-706. doi: 10.1158/0008-5472.can-11-2507. [PMID: 22144471]
  • Man Ho Choi, Ju-Yeon Moon, Sung-Hee Cho, Bong Chul Chung, Eun Jig Lee. Metabolic alteration of urinary steroids in pre- and post-menopausal women, and men with papillary thyroid carcinoma. BMC cancer. 2011 Aug; 11(?):342. doi: 10.1186/1471-2407-11-342. [PMID: 21824401]
  • Maggie Laidlaw, Carla A Cockerline, Daniel W Sepkovic. Effects of a breast-health herbal formula supplement on estrogen metabolism in pre- and post-menopausal women not taking hormonal contraceptives or supplements: a randomized controlled trial. Breast cancer : basic and clinical research. 2010 Dec; 4(?):85-95. doi: 10.4137/bcbcr.s6505. [PMID: 21234288]
  • Emanuela Taioli, Annie Im, Xia Xu, Timothy D Veenstra, Gretchen Ahrendt, Seymour Garte. Comparison of estrogens and estrogen metabolites in human breast tissue and urine. Reproductive biology and endocrinology : RB&E. 2010 Aug; 8(?):93. doi: 10.1186/1477-7827-8-93. [PMID: 20678202]
  • Latanya M Scott, Xia Xu, Timothy D Veenstra, Janet A Tooze, Charles E Wood, Thomas C Register, Nancy D Kock, J Mark Cline. Past oral contraceptive use and current dietary soy isoflavones influence estrogen metabolism in postmenopausal monkeys (Macaca fascicularis). Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology. 2008 Oct; 17(10):2594-602. doi: 10.1158/1055-9965.epi-08-0278. [PMID: 18843000]
  • Xia Xu, John M Roman, Haleem J Issaq, Larry K Keefer, Timothy D Veenstra, Regina G Ziegler. Quantitative measurement of endogenous estrogens and estrogen metabolites in human serum by liquid chromatography-tandem mass spectrometry. Analytical chemistry. 2007 Oct; 79(20):7813-21. doi: 10.1021/ac070494j. [PMID: 17848096]
  • Xia Xu, Larry K Keefer, Regina G Ziegler, Timothy D Veenstra. A liquid chromatography-mass spectrometry method for the quantitative analysis of urinary endogenous estrogen metabolites. Nature protocols. 2007; 2(6):1350-5. doi: 10.1038/nprot.2007.176. [PMID: 17545972]