Etiocholanolone (BioDeep_00000405285)

Main id: BioDeep_00000014343

 

PANOMIX_OTCML-2023


代谢物信息卡片


3alpha-hydroxy-5beta-androstan-17-one

化学式: C19H30O2 (290.224568)
中文名称: 3a-羟基-5b-雄甾烷-17-酮
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: CC12CCC(CC1CCC3C2CCC4(C3CCC4=O)C)O
InChI: InChI=1S/C19H30O2/c1-18-9-7-13(20)11-12(18)3-4-14-15-5-6-17(21)19(15,2)10-8-16(14)18/h12-16,20H,3-11H2,1-2H3/t12-,13-,14+,15+,16+,18+,19+/m1/s1

描述信息

D006730 - Hormones, Hormone Substitutes, and Hormone Antagonists > D006728 - Hormones
C308 - Immunotherapeutic Agent > C2139 - Immunostimulant
COVID info from COVID-19 Disease Map
Corona-virus
Coronavirus
SARS-CoV-2
COVID-19
SARS-CoV
COVID19
SARS2
SARS
Etiocholanolone (5β-Androsterone) is the excreted metabolite of testosterone and has anticonvulsant activity[1]. Etiocholanolone is a less potent?neurosteroid positive allosteric modulator?(PAM) of the GABAA?receptor than its?enantiomer form[2].
Etiocholanolone (5β-Androsterone) is the excreted metabolite of testosterone and has anticonvulsant activity[1]. Etiocholanolone is a less potent?neurosteroid positive allosteric modulator?(PAM) of the GABAA?receptor than its?enantiomer form[2].
Etiocholanolone (5β-Androsterone) is the excreted metabolite of testosterone and has anticonvulsant activity[1]. Etiocholanolone is a less potent?neurosteroid positive allosteric modulator?(PAM) of the GABAA?receptor than its?enantiomer form[2].

同义名列表

5 个代谢物同义名

Etiocholanolone; 3alpha-hydroxy-5beta-androstan-17-one; 5beta-androsterone; ST 19:1;O2; 5β-Androsterone



数据库引用编号

17 个数据库交叉引用编号

分类词条

相关代谢途径

Reactome(1)

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

  • D Susie Lee, Tina Knittel, Tobias Deschner, Michael Heistermann, James P Higham. Testing the role of testosterone versus estrogens in mediating reproductive transitions in female rhesus macaques. Hormones and behavior. 2022 03; 139(?):105123. doi: 10.1016/j.yhbeh.2022.105123. [PMID: 35149292]
  • Thomas Piper, Nadine Haenelt, Gregor Fusshöller, Hans Geyer, Mario Thevis. Sensitive detection of testosterone and testosterone prohormone administrations based on urinary concentrations and carbon isotope ratios of androsterone and etiocholanolone. Drug testing and analysis. 2021 Nov; 13(11-12):1835-1851. doi: 10.1002/dta.3168. [PMID: 34648228]
  • Stefano DE Luca, Eleonora Amante, Cristian Fiori, Giorgio Alleva, Eugenio Alladio, Federico Marini, Diletta Garrou, Matteo Manfredi, Daniele Amparore, Enrico Checcucci, Serena Pruner, Alberto Salomone, Roberto M Scarpa, Marco Vincenti, Francesco Porpiglia. Prospective evaluation of urinary steroids and prostate carcinoma-induced deviation: preliminary results. Minerva urology and nephrology. 2021 02; 73(1):98-106. doi: 10.23736/s2724-6051.19.03529-x. [PMID: 31833333]
  • Dayamin Martinez-Brito, Maria Laura Notarianni, Michele Iannone, Xavier de la Torre, Francesco Botrè. Validation of steroid sulfates deconjugation for metabolic studies. Application to human urine samples. Journal of pharmacological and toxicological methods. 2020 Nov; 106(?):106938. doi: 10.1016/j.vascn.2020.106938. [PMID: 33080389]
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  • Takahiro Maeda, Eiji Kikuchi, Masanori Hasegawa, Keiko Homma, Yota Yasumizu, Seiya Hattori, Takeo Kosaka, Kazunobu Shinoda, Akira Miyajima, Mototsugu Oya. Change of the 5α/5β ratio of urinary steroid metabolites in benign prostatic hyperplasia patients treated with dutasteride. Clinical biochemistry. 2018 May; 55(?):36-41. doi: 10.1016/j.clinbiochem.2018.03.021. [PMID: 29608891]
  • Jingzhu Wang, Yi He, Xin Liu, Zhiyong Yang, Wenning Yang. Steroid profile and IRMS analysis of musk administration for doping control. Drug testing and analysis. 2017 Nov; 9(11-12):1779-1787. doi: 10.1002/dta.2293. [PMID: 28842970]
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  • Clemens Kamrath, Ze'ev Hochberg, Michaela F Hartmann, Thomas Remer, Stefan A Wudy. Increased activation of the alternative "backdoor" pathway in patients with 21-hydroxylase deficiency: evidence from urinary steroid hormone analysis. The Journal of clinical endocrinology and metabolism. 2012 Mar; 97(3):E367-75. doi: 10.1210/jc.2011-1997. [PMID: 22170725]
  • Mario Thevis, Hans Geyer, Gerd Sigmund, Wilhelm Schänzer. Sports drug testing: Analytical aspects of selected cases of suspected, purported, and proven urine manipulation. Journal of pharmaceutical and biomedical analysis. 2012 Jan; 57(?):26-32. doi: 10.1016/j.jpba.2011.09.002. [PMID: 21955645]
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  • Jingzhu Wang, Moutian Wu, Xin Liu, Youxuan Xu. Profiling of urinary steroids by gas chromatography-mass spectrometry detection and confirmation of androstenedione administration using isotope ratio mass spectrometry. Steroids. 2011 Dec; 76(14):1560-5. doi: 10.1016/j.steroids.2011.09.007. [PMID: 21945895]
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