Benzyloxyresorufin (BioDeep_00000720830)

   


代谢物信息卡片


Resorufin benzyl ether

化学式: C19H13NO3 (303.0895)
中文名称: 苄氧基试卤灵
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: C1=CC=C(C=C1)COC2=CC3=C(C=C2)N=C4C=CC(=O)C=C4O3
InChI: InChI=1S/C19H13NO3/c21-14-6-8-16-18(10-14)23-19-11-15(7-9-17(19)20-16)22-12-13-4-2-1-3-5-13/h1-11H,12H2

描述信息

同义名列表

2 个代谢物同义名

Resorufin benzyl ether; Benzyloxyresorufin



数据库引用编号

2 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。

亚细胞结构定位 关联基因列表


文献列表

  • Lukas Rutz, Lan Gao, Jan-Heiner Küpper, Dieter Schrenk. Structure-dependent genotoxic potencies of selected pyrrolizidine alkaloids in metabolically competent HepG2 cells. Archives of toxicology. 2020 12; 94(12):4159-4172. doi: 10.1007/s00204-020-02895-z. [PMID: 32910235]
  • Byung Hee Han, Meng-liang Zhou, Ananth K Vellimana, Eric Milner, David H Kim, Jacob K Greenberg, Wenhua Chu, Robert H Mach, Gregory J Zipfel. Resorufin analogs preferentially bind cerebrovascular amyloid: potential use as imaging ligands for cerebral amyloid angiopathy. Molecular neurodegeneration. 2011 Dec; 6(?):86. doi: 10.1186/1750-1326-6-86. [PMID: 22192811]
  • Lisa B Helgason, Augustine Arukwe, Geir W Gabrielsen, Mikael Harju, Marit N Hegseth, Eldbjørg S Heimstad, Even H Jørgensen, Anne S Mortensen, Johannes Wolkers. Biotransformation of PCBs in Arctic seabirds: characterization of phase I and II pathways at transcriptional, translational and activity levels. Comparative biochemistry and physiology. Toxicology & pharmacology : CBP. 2010 Jun; 152(1):34-41. doi: 10.1016/j.cbpc.2010.02.009. [PMID: 20176133]
  • Robert D Finn, Lesley A McLaughlin, Sebastien Ronseaux, Ian Rosewell, J Brian Houston, Colin J Henderson, C Roland Wolf. Defining the in Vivo Role for cytochrome b5 in cytochrome P450 function through the conditional hepatic deletion of microsomal cytochrome b5. The Journal of biological chemistry. 2008 Nov; 283(46):31385-93. doi: 10.1074/jbc.m803496200. [PMID: 18805792]
  • L A McLaughlin, U Niazi, J Bibby, J-P David, J Vontas, J Hemingway, H Ranson, M J Sutcliffe, M J I Paine. Characterization of inhibitors and substrates of Anopheles gambiae CYP6Z2. Insect molecular biology. 2008 Apr; 17(2):125-35. doi: 10.1111/j.1365-2583.2007.00788.x. [PMID: 18353102]
  • Reddy P Kommaddi, Cheri M Turman, Bhagavatula Moorthy, Lihua Wang, Henry W Strobel, Vijayalakshmi Ravindranath. An alternatively spliced cytochrome P4501A1 in human brain fails to bioactivate polycyclic aromatic hydrocarbons to DNA-reactive metabolites. Journal of neurochemistry. 2007 Aug; 102(3):867-77. doi: 10.1111/j.1471-4159.2007.04599.x. [PMID: 17630984]
  • Sasan Mosadeghi, Bjarte Furnes, Aline Y O Matsuo, Daniel Schlenk. Expression and characterization of cytochrome P450 2X1 in channel catfish (Ictalurus punctatus). Biochimica et biophysica acta. 2007 Jul; 1770(7):1045-52. doi: 10.1016/j.bbagen.2007.03.008. [PMID: 17459590]
  • Bertrand Piver, François Berthou, Yvonne Dreano, Danièle Lucas. Differential inhibition of human cytochrome P450 enzymes by epsilon-viniferin, the dimer of resveratrol: comparison with resveratrol and polyphenols from alcoholized beverages. Life sciences. 2003 Jul; 73(9):1199-213. doi: 10.1016/s0024-3205(03)00420-x. [PMID: 12818727]
  • H Y Yang, Q P Lee, A E Rettie, M R Juchau. Functional cytochrome P4503A isoforms in human embryonic tissues: expression during organogenesis. Molecular pharmacology. 1994 Nov; 46(5):922-8. doi: NULL. [PMID: 7969081]
  • R W Nims, R M McClain, P S Manchand, P S Belica, P E Thomas, D W Mellini, W E Utermahlen, R A Lubet. Comparative pharmacodynamics of hepatic cytochrome P450 2B induction by 5,5-diphenyl- and 5,5-diethyl-substituted barbiturates and hydantoins in the male F344/NCr rat. The Journal of pharmacology and experimental therapeutics. 1994 Jul; 270(1):348-55. doi: . [PMID: 8035330]
  • P V Nerurkar, S S Park, P E Thomas, R W Nims, R A Lubet. Methoxyresorufin and benzyloxyresorufin: substrates preferentially metabolized by cytochromes P4501A2 and 2B, respectively, in the rat and mouse. Biochemical pharmacology. 1993 Sep; 46(5):933-43. doi: 10.1016/0006-2952(93)90504-p. [PMID: 8373445]