1,2,6-Trigalloylglucose (BioDeep_00001869090)

Main id: BioDeep_00000005494

 

Volatile Flavor Compounds


代谢物信息卡片


1,2,6-Trigalloylglucose

化学式: C27H24O18 (636.0962604)
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)OCC2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)O)O
InChI: InChI=1S/C27H24O18/c28-11-1-8(2-12(29)18(11)34)24(39)42-7-17-21(37)22(38)23(44-25(40)9-3-13(30)19(35)14(31)4-9)27(43-17)45-26(41)10-5-15(32)20(36)16(33)6-10/h1-6,17,21-23,27-38H,7H2/t17-,21-,22+,23-,27+/m1/s1

描述信息

同义名列表

2 个代谢物同义名

1,2,6-Trigalloylglucose; 1-O,2-O,6-O-Trigalloyl-beta-D-glucose



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)

27 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

  • Divinah K Nyamboki, Kibrom G Bedane, Khadija Hassan, Lukas Brieger, Carsten Strohmann, Michael Spiteller, Josphat C Matasyoh. Cytotoxic Compounds from the Stem Bark of Two subsp. of Bersama abyssinica. Journal of natural products. 2021 05; 84(5):1453-1458. doi: 10.1021/acs.jnatprod.0c01141. [PMID: 33974421]
  • Kang Wei, Huafeng He, Hailin Li, Liyuan Wang, Li Ruan, Dandan Pang, Hao Cheng. Gallotannin 1,2,6-tri-O-galloyl-β-d-glucopyranose: Its availability and changing patterns in tea (Camellia sinensis). Food chemistry. 2019 Oct; 296(?):40-46. doi: 10.1016/j.foodchem.2019.05.144. [PMID: 31202304]
  • A Bag, S K Bhattacharyya, R R Chattopadhyay. Isolation and identification of a gallotannin 1,2,6-tri-O-galloyl-β-D-glucopyranose from hydroalcoholic extract of Terminalia chebula fruits effective against multidrug-resistant uropathogens. Journal of applied microbiology. 2013 Aug; 115(2):390-7. doi: 10.1111/jam.12256. [PMID: 23683054]
  • Mohamed A A Orabi, Shoko Taniguchi, Morio Yoshimura, Takashi Yoshida, Kaori Kishino, Hiroshi Sakagami, Tsutomu Hatano. Hydrolyzable tannins of tamaricaceous plants. III. Hellinoyl- and macrocyclic-type ellagitannins from Tamarix nilotica. Journal of natural products. 2010 May; 73(5):870-9. doi: 10.1021/np900829g. [PMID: 20405847]
  • Yuanyuan Xie, Toshio Morikawa, Kiyofumi Ninomiya, Katsuya Imura, Osamu Muraoka, Dan Yuan, Masayuki Yoshikawa. Medicinal flowers. XXIII. New taraxastane-type triterpene, punicanolic acid, with tumor necrosis factor-alpha inhibitory activity from the flowers of Punica granatum. Chemical & pharmaceutical bulletin. 2008 Nov; 56(11):1628-31. doi: 10.1248/cpb.56.1628. [PMID: 18981621]
  • Deliang Duan, Zhengquan Li, Hongpeng Luo, Wei Zhang, Lirong Chen, Xiaojie Xu. Antiviral compounds from traditional Chinese medicines Galla Chinese as inhibitors of HCV NS3 protease. Bioorganic & medicinal chemistry letters. 2004 Dec; 14(24):6041-4. doi: 10.1016/j.bmcl.2004.09.067. [PMID: 15546725]
  • I Abe, Y Kashiwagi, H Noguchi, T Tanaka, Y Ikeshiro, Y Kashiwada. Ellagitannins and hexahydroxydiphenoyl esters as inhibitors of vertebrate squalene epoxidase. Journal of natural products. 2001 Aug; 64(8):1010-4. doi: 10.1021/np010100y. [PMID: 11520216]
  • H J Kim, E R Woo, C G Shin, H Park. A new flavonol glycoside gallate ester from Acer okamotoanum and its inhibitory activity against human immunodeficiency virus-1 (HIV-1) integrase. Journal of natural products. 1998 Jan; 61(1):145-8. doi: 10.1021/np970171q. [PMID: 9461665]