naphthyl glucuronide (BioDeep_00000008740)

 

Secondary id: BioDeep_00000845175


代谢物信息卡片


(2S,3S,4S,5R)-3,4,5-trihydroxy-6-naphthalen-1-yloxyoxane-2-carboxylic acid

化学式: C16H16O7 (320.0895986)
中文名称:
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: O=C(O)C1OC(Oc2cccc3ccccc23)C(O)C(O)C1O
InChI:

描述信息

同义名列表

6 个代谢物同义名

(2S,3S,4S,5R)-3,4,5-trihydroxy-6-naphthalen-1-yloxyoxane-2-carboxylic acid; alpha-Naphthyl-beta-D-glucuronide; 1-Naphthyl β-D-glucuronide; 1-NAPHTHYL B-D-GLUCURONIDE; 1-Naphthyl glucuronide; naphthyl glucuronide



数据库引用编号

9 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

  • Junichi Narukawa, Hiroki Inoue, Seiyu Kato, Hiroshi Yokota. Glucuronidation of 1-naphthol and excretion into the vein in perfused rat kidney. Drug metabolism and disposition: the biological fate of chemicals. 2004 Jul; 32(7):758-61. doi: 10.1124/dmd.32.7.758. [PMID: 15205392]
  • Rémon A M H van Aubel, Pascal H E Smeets, Janny G P Peters, René J M Bindels, Frans G M Russel. The MRP4/ABCC4 gene encodes a novel apical organic anion transporter in human kidney proximal tubules: putative efflux pump for urinary cAMP and cGMP. Journal of the American Society of Nephrology : JASN. 2002 Mar; 13(3):595-603. doi: 10.1681/asn.v133595. [PMID: 11856762]
  • M H de Vries, F A Redegeld, A S Koster, J Noordhoek, J G de Haan, R P Oude Elferink, P L Jansen. Hepatic, intestinal and renal transport of 1-naphthol-beta-D-glucuronide in mutant rats with hereditary-conjugated hyperbilirubinemia. Naunyn-Schmiedeberg's archives of pharmacology. 1989 Nov; 340(5):588-92. doi: 10.1007/bf00260615. [PMID: 2615850]
  • J E Keiser, L J Prokuski, V S Ong. An enzymatic method for the hydrolysis of urinary 1-naphthyl glucuronide. Bulletin of environmental contamination and toxicology. 1988 Aug; 41(2):159-63. doi: 10.1007/bf01705425. [PMID: 3207897]
  • F A Redegeld, J Noordhoek. Active tubular secretion of 1-naphthyl-beta-D-glucuronide in the isolated perfused rat kidney. Drug metabolism and disposition: the biological fate of chemicals. 1986 Sep; 14(5):622-4. doi: NULL. [PMID: 2876872]
  • L M Tremaine, G L Diamond, A J Quebbemann. Quantitative determination of organ contribution to excretory metabolism. Journal of pharmacological methods. 1985 Feb; 13(1):9-35. doi: 10.1016/0160-5402(85)90064-6. [PMID: 3974258]
  • G F Rush, J B Hook. Characteristics of renal UDP-glucuronyltransferase. Life sciences. 1984 Jul; 35(2):145-53. doi: 10.1016/0024-3205(84)90133-4. [PMID: 6429466]
  • W H Chern, W C Dauterman. Studies on the metabolism and excretion of 1-naphthol, 1-naphthyl-beta-D-glucuronide, and 1-naphthyl-beta-D-glucoside in the mouse. Toxicology and applied pharmacology. 1983 Mar; 67(3):303-9. doi: 10.1016/0041-008x(83)90313-7. [PMID: 6845360]
  • J C Rhodes, J B Houston. Quantification of naphthyl conjugates. Comparison of high-performance liquid chromatography and selective enzyme hydrolysis methods. Xenobiotica; the fate of foreign compounds in biological systems. 1981 Jan; 11(1):63-70. doi: 10.3109/00498258109045273. [PMID: 7222731]
  • W TROLL, S BELMAN, N NELSON, M LEVITZ, G H TWOMBLY. Aromatic amines. II. Demonstration of 2-amino-1-naphthyl glucuronides as metabolite of 2-naphthylamine in dog urine. Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine (New York, N.Y.). 1959 Jan; 100(1):75-8. doi: 10.3181/00379727-100-24529. [PMID: 13634041]