(+)-2-(Benzothiophen-4-yl)-N-methyl-N-((1R,2R)-2-pyrrolidin-1-ylcyclohexyl)acetamide (BioDeep_00000171500)

   

human metabolite blood metabolite


代谢物信息卡片


(+)-2-(Benzothiophen-4-yl)-N-methyl-N-((1R,2R)-2-pyrrolidin-1-ylcyclohexyl)acetamide

化学式: C21H28N2OS (356.1922)
中文名称:
谱图信息: 最多检出来源 Homo sapiens(blood) 100%

分子结构信息

SMILES: CN(C1CCCCC1N1CCCC1)C(=O)CC1=C2C=CSC2=CC=C1
InChI: InChI=1S/C21H28N2OS/c1-22(18-8-2-3-9-19(18)23-12-4-5-13-23)21(24)15-16-7-6-10-20-17(16)11-14-25-20/h6-7,10-11,14,18-19H,2-5,8-9,12-13,15H2,1H3



数据库引用编号

3 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

  • M J A Walker, E S Hayes, D A Saint, G Adaikan, S Abraham, A L Goldin, G N Beatch, B A MacLeod, R A Wall, M K Pugsley. Pharmacological and toxicological activity of RSD921, a novel sodium channel blocker. Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie. 2018 Oct; 106(?):510-522. doi: 10.1016/j.biopha.2018.06.157. [PMID: 29990839]
  • W Ribeiro, D R Ifa, G Corso, J Salmon, L A Moraes, M N Eberlin, G de Nucci. Determination of RSD921 in human plasma by high-performance liquid chromatography-tandem mass spectrometry using tri-deuterated RSD921 as internal standard: application to a phase I clinical trial. Journal of mass spectrometry : JMS. 2001 Oct; 36(10):1133-9. doi: 10.1002/jms.218. [PMID: 11747107]
  • S M Moussaoui, F Montier, A Carruette, J C Blanchard, P M Laduron, C Garret. A non-peptide NK1-receptor antagonist, RP 67580, inhibits neurogenic inflammation postsynaptically. British journal of pharmacology. 1993 May; 109(1):259-64. doi: 10.1111/j.1476-5381.1993.tb13562.x. [PMID: 7684305]
  • M D Lee, P G Clifton. Free-feeding and free-drinking patterns of male rats following treatment with opiate kappa agonists. Physiology & behavior. 1992 Dec; 52(6):1179-85. doi: 10.1016/0031-9384(92)90479-l. [PMID: 1336603]
  • R F Parrott, I S Ebenezer, B A Baldwin, M L Forsling. Hormonal effects of apomorphine and cholecystokinin in pigs: modification of the response to cholecystokinin by a dopamine antagonist (metoclopramide) and a kappa opioid agonist (PD117302). Acta endocrinologica. 1991 Oct; 125(4):420-6. doi: 10.1530/acta.0.1250420. [PMID: 1957561]
  • M Gué, M Alvinerie, J L Junien, L Buéno. Stimulation of kappa opiate receptors in intestinal wall affects stress-induced increase of plasma cortisol in dogs. Brain research. 1989 Nov; 502(1):143-8. doi: 10.1016/0006-8993(89)90469-1. [PMID: 2555024]
  • G Bianchi. High-performance liquid chromatographic assay of k-opioid selective benzeneacetamide derivatives (U50488, U69593 and PD117302) in rat plasma and brain. Journal of chromatography. 1989 Jul; 491(2):481-7. doi: 10.1016/s0378-4347(00)82869-8. [PMID: 2553762]