Zolasartan (BioDeep_00000674563)

   


代谢物信息卡片


3-[[3-bromo-2-[2-(2H-tetrazol-5-yl)phenyl]-1-benzofuran-5-yl]methyl]-2-butyl-5-chloroimidazole-4-carboxylic acid

化学式: C24H20BrClN6O3 (554.04687)
中文名称: 佐拉沙坦
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: CCCCC1=NC(=C(N1CC2=CC3=C(C=C2)OC(=C3Br)C4=CC=CC=C4C5=NNN=N5)C(=O)O)Cl
InChI: InChI=1S/C24H20BrClN6O3/c1-2-3-8-18-27-22(26)20(24(33)34)32(18)12-13-9-10-17-16(11-13)19(25)21(35-17)14-6-4-5-7-15(14)23-28-30-31-29-23/h4-7,9-11H,2-3,8,12H2,1H3,(H,33,34)(H,28,29,30,31)

描述信息

C78274 - Agent Affecting Cardiovascular System > C270 - Antihypertensive Agent > C66930 - Angiotensin II Receptor Antagonist
D057911 - Angiotensin Receptor Antagonists > D047228 - Angiotensin II Type 1 Receptor Blockers

同义名列表

2 个代谢物同义名

3-[[3-bromo-2-[2-(2H-tetrazol-5-yl)phenyl]-1-benzofuran-5-yl]methyl]-2-butyl-5-chloroimidazole-4-carboxylic acid; Zolasartan



数据库引用编号

4 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)

0 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

  • C Tebbs, M K Pratten, F Broughton Pipkin. Angiotensin II is a growth factor in the peri-implantation rat embryo. Journal of anatomy. 1999 Jul; 195 ( Pt 1)(?):75-86. doi: 10.1046/j.1469-7580.1999.19510075.x. [PMID: 10473295]
  • R J Cannell, A R Knaggs, M J Dawson, G R Manchee, P J Eddershaw, I Waterhouse, D R Sutherland, G D Bowers, P J Sidebottom. Microbial biotransformation of the angiotensin II antagonist GR117289 by Streptomyces rimosus to identify a mammalian metabolite. Drug metabolism and disposition: the biological fate of chemicals. 1995 Jul; 23(7):724-9. doi: NULL. [PMID: 7587961]
  • D B Judd, M D Dowle, D Middlemiss, D I Scopes, B C Ross, T I Jack, M Pass, E Tranquillini, J E Hobson, T A Panchal. Bromobenzofuran-based non-peptide antagonists of angiotensin II: GR138950, a potent antihypertensive agent with high oral bioavailability. Journal of medicinal chemistry. 1994 Sep; 37(19):3108-20. doi: 10.1021/jm00045a016. [PMID: 7932534]
  • G S Murkitt, E Z Trafankowska, M Dunne, G R Manchee. Fully automated assay for the determination of GR117289X in human plasma using mixed mode solid-phase extraction and high-performance liquid chromatography with ultraviolet detection. Journal of pharmaceutical and biomedical analysis. 1994 Sep; 12(9):1181-7. doi: 10.1016/0731-7085(94)e0032-v. [PMID: 7803570]
  • K L Clark, M J Robertson, G M Drew. Role of angiotensin AT1 and AT2 receptors in mediating the renal effects of angiotensin II in the anaesthetized dog. British journal of pharmacology. 1993 May; 109(1):148-56. doi: 10.1111/j.1476-5381.1993.tb13545.x. [PMID: 8495237]
  • M J Robertson, J C Barnes, G M Drew, K L Clark, F H Marshall, A Michel, D Middlemiss, B C Ross, D Scopes, M D Dowle. Pharmacological profile of GR117289 in vitro: a novel, potent and specific non-peptide angiotensin AT1 receptor antagonist. British journal of pharmacology. 1992 Dec; 107(4):1173-80. doi: 10.1111/j.1476-5381.1992.tb13425.x. [PMID: 1467838]