[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] 3,4,5-trihydroxybenzoate (BioDeep_00001875798)

   


代谢物信息卡片


[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] 3,4,5-trihydroxybenzoate

化学式: C13H16O10 (332.0743436)
中文名称:
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: C1=C(C=C(C(=C1O)O)O)C(=O)OC2C(C(C(C(O2)CO)O)O)O
InChI: InChI=1S/C13H16O10/c14-3-7-9(18)10(19)11(20)13(22-7)23-12(21)4-1-5(15)8(17)6(16)2-4/h1-2,7,9-11,13-20H,3H2

描述信息

同义名列表

1 个代谢物同义名

[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] 3,4,5-trihydroxybenzoate



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)

5 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

  • Muthenna Puppala, Jessica Ponder, Palla Suryanarayana, Geereddy Bhanuprakash Reddy, J Mark Petrash, Daniel V LaBarbera. The isolation and characterization of β-glucogallin as a novel aldose reductase inhibitor from Emblica officinalis. PloS one. 2012; 7(4):e31399. doi: 10.1371/journal.pone.0031399. [PMID: 22485126]
  • Jody K Takemoto, Neal M Davies. Method development for β-glucogallin and gallic acid analysis: application to urinary pharmacokinetic studies. Journal of pharmaceutical and biomedical analysis. 2011 Mar; 54(4):812-6. doi: 10.1016/j.jpba.2010.11.003. [PMID: 21130594]
  • Viviane Cândida da Silva, Assunta Napolitano, Daniela Eletto, Clenilson Martins Rodrigues, Cosimo Pizza, Wagner Vilegas. Characterization of gallotannins from Astronium species by flow injection analysis- electrospray ionization-ion trap-tandem mass spectrometry and matrix-assisted laser desorption/ionization time-of- flight mass spectrometry. European journal of mass spectrometry (Chichester, England). 2011; 17(4):365-75. doi: 10.1255/ejms.1141. [PMID: 22006629]
  • Jun Lee, Dae Sik Jang, Nan Hee Kim, Yun Mi Lee, Junghyun Kim, Jin Sook Kim. Galloyl glucoses from the seeds of Cornus officinalis with inhibitory activity against protein glycation, aldose reductase, and cataractogenesis ex vivo. Biological & pharmaceutical bulletin. 2011; 34(3):443-6. doi: 10.1248/bpb.34.443. [PMID: 21372401]
  • Rokia Sanogo, Antonio Vassallo, Nicola Malafronte, Salvatore Imparato, Alessandra Russo, Fabrizio Dal Piaz. New phenolic glycosides from Securinega virosa and their antioxidant activity. Natural product communications. 2009 Dec; 4(12):1645-50. doi: ". [PMID: 20120099]
  • Song-Lin Li, Jing-Zheng Song, Franky F K Choi, Chun-Feng Qiao, Yan Zhou, Quan-Bin Han, Hong-Xi Xu. Chemical profiling of Radix Paeoniae evaluated by ultra-performance liquid chromatography/photo-diode-array/quadrupole time-of-flight mass spectrometry. Journal of pharmaceutical and biomedical analysis. 2009 Feb; 49(2):253-66. doi: 10.1016/j.jpba.2008.11.007. [PMID: 19097720]
  • Lu Chen, Dawei Wang, Jie Wu, Boyang Yu, Danni Zhu. Identification of multiple constituents in the traditional Chinese medicine formula GuiZhiFuLing-Wan by HPLC-DAD-MS/MS. Journal of pharmaceutical and biomedical analysis. 2009 Feb; 49(2):267-75. doi: 10.1016/j.jpba.2008.11.012. [PMID: 19095393]
  • E-Hu Liu, Lian-Wen Qi, Bin Li, Yong-Bo Peng, Ping Li, Chang-Yin Li, Jun Cao. High-speed separation and characterization of major constituents in Radix Paeoniae Rubra by fast high-performance liquid chromatography coupled with diode-array detection and time-of-flight mass spectrometry. Rapid communications in mass spectrometry : RCM. 2009 Jan; 23(1):119-30. doi: 10.1002/rcm.3848. [PMID: 19065578]
  • Claire Dufour, Eric Da Silva, Pierre Potier, Yves Queneau, Olivier Dangles. Gallic esters of sucrose as efficient radical scavengers in lipid peroxidation. Journal of agricultural and food chemistry. 2002 Jun; 50(12):3425-30. doi: 10.1021/jf011683k. [PMID: 12033806]
  • Mi-Jeong Ahn, Chul Young Kim, Ji Suk Lee, Tae Gyun Kim, Seung Hee Kim, Chong-Kyo Lee, Bo-Bin Lee, Cha-Gyun Shin, Hoon Huh, Jinwoong Kim. Inhibition of HIV-1 integrase by galloyl glucoses from Terminalia chebula and flavonol glycoside gallates from Euphorbia pekinensis. Planta medica. 2002 May; 68(5):457-9. doi: 10.1055/s-2002-32070. [PMID: 12058327]
  • T Iwakawa, Y Tanaka, A Takashima. A new galloylglucoside from Cleyera ochnacea DC. Chemical & pharmaceutical bulletin. 2001 Nov; 49(11):1498-9. doi: 10.1248/cpb.49.1498. [PMID: 11724249]
  • N Tanaka, K Shimomura, K Ishimaru. Ellagic acid formation from galloylglucoses by a crude enzyme of Cornus capitata adventitious roots. Bioscience, biotechnology, and biochemistry. 2001 Aug; 65(8):1869-71. doi: 10.1271/bbb.65.1869. [PMID: 11577731]
  • J W Hubbard, K K Midha, J K Cooper. The metabolism of p-methoxyamphetamine in dog and monkey. O-demethylation as a major route. Drug metabolism and disposition: the biological fate of chemicals. 1977 Jul; 5(4):329-34. doi: NULL. [PMID: 19212]
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