Quercetin 7-glucoside (BioDeep_00000009367)

 

Secondary id: BioDeep_00000019579, BioDeep_00000230292

human metabolite PANOMIX_OTCML-2023 Volatile Flavor Compounds natural product


代谢物信息卡片


2-(3,4-dihydroxyphenyl)-3,5-dihydroxy-7-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-4H-chromen-4-one

化学式: C21H20O12 (464.09547200000003)
中文名称: 槲皮素-7-O-β-D-葡萄糖苷, 槲皮素-7-O-BETA-D-吡喃葡萄糖苷
谱图信息: 最多检出来源 Viridiplantae(plant) 5.23%

分子结构信息

SMILES: c1(cc(c2c(c1)oc(c(c2=O)O)c1ccc(c(c1)O)O)O)O[C@H]1[C@@H]([C@H]([C@@H]([C@H](O1)CO)O)O)O
InChI: InChI=1S/C21H20O12/c22-6-13-15(26)17(28)19(30)21(33-13)31-8-4-11(25)14-12(5-8)32-20(18(29)16(14)27)7-1-2-9(23)10(24)3-7/h1-5,13,15,17,19,21-26,28-30H,6H2/t13-,15-,17+,19-,21-/m1/s1

描述信息

Quercetin 7-glucoside, also known as quercimeritrin, is a member of the class of compounds known as flavonoid-7-o-glycosides. Flavonoid-7-o-glycosides are phenolic compounds containing a flavonoid moiety which is O-glycosidically linked to carbohydrate moiety at the C7-position. Quercetin 7-glucoside is slightly soluble (in water) and a very weakly acidic compound (based on its pKa). Quercetin 7-glucoside can be found in a number of food items such as roman camomile, okra, dandelion, and cottonseed, which makes quercetin 7-glucoside a potential biomarker for the consumption of these food products.
Quercimeritrin, isolated from the leaves of Ixeridium dentatum, exhibits significant amylase activity[1].
Quercimeritrin, isolated from the leaves of Ixeridium dentatum, exhibits significant amylase activity[1].

同义名列表

17 个代谢物同义名

2-(3,4-dihydroxyphenyl)-3,5-dihydroxy-7-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-4H-chromen-4-one; 2-(3,4-Dihydroxyphenyl)-7-(beta-D-glucopyranosyloxy)-3,5-dihydroxy-4H-1-benzopyran-4-one; 3,5-Dihydroxy-2-(3,4-dihydroxyphenyl)-7-(beta-D-glucopyranosyloxy)-4H-1-benzopyran-4-one; 3,5-Dihydroxy-2-(3,4-dihydroxyphenyl)-7-(β-D-glucopyranosyloxy)-4H-1-benzopyran-4-one; 3,5-Dihydroxy-2-(3,4-dihydroxyphenyl)-7-(b-D-glucopyranosyloxy)-4H-1-benzopyran-4-one; 2-(3,4-Dihydroxyphenyl)-7-(b-D-glucopyranosyloxy)-3,5-dihydroxy-4H-1-benzopyran-4-one; 2-(3,4-Dihydroxyphenyl)-7-(β-D-glucopyranosyloxy)-3,5-dihydroxy-4H-1-benzopyran-4-one; Quercetin 7-O-beta-D-glucoside; Quercetin 7-O-β-D-glucoside; Quercetin 7-O-b-D-glucoside; quercetin 7-O-glucoside; quercetin-7-O-glucoside; Quercetin 7-glucoside; Quercimeritroside; Quercimeritrin; Quercetin-7-O-β-D-glucopyranoside; Quercimeritrin



数据库引用编号

17 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)

250 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

  • SeonJu Park, Nguyen Xuan Nhiem, Jun Hyung Park, Kashi Raj Bhattarai, Han-Jung Chae, Hyung-Ryong Kim, Seung Hyun Kim. Isolation of amylase regulators from the leaves of Ixeridium dentatum. Natural product research. 2021 Mar; 35(5):744-749. doi: 10.1080/14786419.2019.1599885. [PMID: 30966790]
  • Enkhtaivan Gansukh, Zakayo Kazibwe, Muthuraman Pandurangan, Gopal Judy, Doo Hwan Kim. Probing the impact of quercetin-7-O-glucoside on influenza virus replication influence. Phytomedicine : international journal of phytotherapy and phytopharmacology. 2016 Aug; 23(9):958-67. doi: 10.1016/j.phymed.2016.06.001. [PMID: 27387404]
  • Bui Thi Thuy Luyen, Bui Huu Tai, Nguyen Phuong Thao, Ji Yun Cha, Hoon Yeon Lee, Young Mi Lee, Young Ho Kim. Anti-inflammatory components of Chrysanthemum indicum flowers. Bioorganic & medicinal chemistry letters. 2015 Jan; 25(2):266-9. doi: 10.1016/j.bmcl.2014.11.054. [PMID: 25497988]
  • Filis Morina, Umeo Takahama, Ryo Yamauchi, Sachiko Hirota, Sonja Veljovic-Jovanovic. Quercetin 7-O-glucoside suppresses nitrite-induced formation of dinitrosocatechins and their quinones in catechin/nitrite systems under stomach simulating conditions. Food & function. 2015 Jan; 6(1):219-29. doi: 10.1039/c4fo00695j. [PMID: 25375233]
  • Tian-Tian Zhang, Chuan-Li Lu, Jian-Guo Jiang. Bioactivity evaluation of ingredients identified from the fruits of Amomum tsaoko Crevost et Lemaire, a Chinese spice. Food & function. 2014 Aug; 5(8):1747-54. doi: 10.1039/c4fo00169a. [PMID: 24915829]
  • Tamara R Calvo, Diego Demarco, Fabio V Santos, Helen P Moraes, Taís M Bauab, Eliana A Varanda, Ilce M S Cólus, Wagner Vilegas. Phenolic compounds in leaves of Alchornea triplinervia: anatomical localization, mutagenicity, and antibacterial activity. Natural product communications. 2010 Aug; 5(8):1225-32. doi: . [PMID: 20839624]
  • Deepak Kumar Semwal, Usha Rawat, Ravindra Semwal, Randhir Singh, Pawan Krishan, Manjeet Singh, Gur Jas Preet Singh. Chemical constituents from the leaves of Boehmeria rugulosa with antidiabetic and antimicrobial activities. Journal of Asian natural products research. 2009 Dec; 11(12):1045-55. doi: 10.1080/10286020903352526. [PMID: 20183275]
  • Young Jae Lee, Sungun Kim, Seung Jae Lee, Inhye Ham, Wan Kyunn Whang. Antioxidant activities of new flavonoids from Cudrania tricuspidata root bark. Archives of pharmacal research. 2009 Feb; 32(2):195-200. doi: 10.1007/s12272-009-1135-z. [PMID: 19280148]
  • Wei-li Han, Li Liu, Xiao-qi Zhang, Wen-cai Ye, Yi-le Pan, Xin-sheng Yao. [Chemical constituents from leaves of Morus multicaulis]. Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica. 2007 Apr; 32(8):695-8. doi: . [PMID: 17608222]
  • M G de Carvalho, D C Cranchi, D G Kingston, A A Werle. Proposed active constituents of Dipladenia martiana. Phytotherapy research : PTR. 2001 Dec; 15(8):715-7. doi: 10.1002/ptr.865. [PMID: 11746866]
  • E Luiz da Silva, T Tsushida, J Terao. Inhibition of mammalian 15-lipoxygenase-dependent lipid peroxidation in low-density lipoprotein by quercetin and quercetin monoglucosides. Archives of biochemistry and biophysics. 1998 Jan; 349(2):313-20. doi: 10.1006/abbi.1997.0455. [PMID: 9448720]