1-(5-Fluoropentyl)-1H-indole-3-carboxylic acid 8-quinolinyl ester (BioDeep_00000172812)

   

human metabolite blood metabolite


代谢物信息卡片


1-(5-Fluoropentyl)-1H-indole-3-carboxylic acid 8-quinolinyl ester

化学式: C23H21FN2O2 (376.15869779999997)
中文名称: 1-(5-氟戊基)-1H-吲哚-3-羧酸8-喹啉基酯
谱图信息: 最多检出来源 Homo sapiens(blood) 96.36%

分子结构信息

SMILES: C1=CC=C2C(=C1)C(=CN2CCCCCF)C(=O)OC3=CC=CC4=C3N=CC=C4
InChI: InChI=1S/C23H21FN2O2/c24-13-4-1-5-15-26-16-19(18-10-2-3-11-20(18)26)23(27)28-21-12-6-8-17-9-7-14-25-22(17)21/h2-3,6-12,14,16H,1,4-5,13,15H2

描述信息

D006730 - Hormones, Hormone Substitutes, and Hormone Antagonists > D006728 - Hormones > D063385 - Cannabinoid Receptor Modulators
D018377 - Neurotransmitter Agents > D063385 - Cannabinoid Receptor Modulators > D063386 - Cannabinoid Receptor Agonists

同义名列表

9 个代谢物同义名

1-(5-Fluoropentyl)-1H-indole-3-carboxylic acid 8-quinolinyl ester; 1-(5-Fluoropentyl)-1H-indole-3-carboxylate 8-quinolinyl ester; 1-Pentyfluoro-1H-indole-3-carboxylic acid 8-quinolinyl ester; quinolin-8-yl 1-(5-fluoropentyl)-1H-indole-3-carboxylate; quinolin-8-yl 1-(5-fluoropentyl)indole-3-carboxylate; 5F-PB-22 Compound; 5-fluoro-PB-22; 5F-PB-22; 1-(5-Fluoropentyl)-1H-indole-3-carboxylic acid 8-quinolinyl ester



数据库引用编号

5 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。



文献列表

  • Lilian H J Richter, Andreas Beck, Veit Flockerzi, Hans H Maurer, Markus R Meyer. Cytotoxicity of new psychoactive substances and other drugs of abuse studied in human HepG2 cells using an adopted high content screening assay. Toxicology letters. 2019 Feb; 301(?):79-89. doi: 10.1016/j.toxlet.2018.11.007. [PMID: 30465810]
  • Annelies Cannaert, Jolien Storme, Florian Franz, Volker Auwärter, Christophe P Stove. Detection and Activity Profiling of Synthetic Cannabinoids and Their Metabolites with a Newly Developed Bioassay. Analytical chemistry. 2016 12; 88(23):11476-11485. doi: 10.1021/acs.analchem.6b02600. [PMID: 27779402]
  • Rachelle Abouchedid, James H Ho, Simon Hudson, Alison Dines, John R H Archer, David M Wood, Paul I Dargan. Acute Toxicity Associated with Use of 5F-Derivations of Synthetic Cannabinoid Receptor Agonists with Analytical Confirmation. Journal of medical toxicology : official journal of the American College of Medical Toxicology. 2016 12; 12(4):396-401. doi: 10.1007/s13181-016-0571-7. [PMID: 27456262]