Luteolin 7-O-[beta-D-glucuronosyl-(1->2)-beta-D-glucuronide] (BioDeep_00000396935)

 

Secondary id: BioDeep_00000004070, BioDeep_00000268900, BioDeep_00000628642

human metabolite PANOMIX_OTCML-2023 Endogenous blood metabolite


代谢物信息卡片


(2S,3S,4S,5R,6R)-6-(((2S,3R,4S,5S,6S)-6-Carboxy-2-((2-(3,4-dihydroxyphenyl)-5-hydroxy-4-oxo-4H-chromen-7-yl)oxy)-4,5-dihydroxytetrahydro-2H-pyran-3-yl)oxy)-3,4,5-trihydroxytetrahydro-2H-pyran-2-carboxylic acid

化学式: C27H26O18 (638.1119096)
中文名称: 木犀草素7-地葡萄糖醛酸
谱图信息: 最多检出来源 Homo sapiens(blood) 22.16%

分子结构信息

SMILES: c1(cc(c2c(c1)oc(cc2=O)c1ccc(c(c1)O)O)O)O[C@@H]1O[C@@H]([C@H]([C@@H]([C@H]1O[C@H]1[C@@H]([C@H]([C@@H]([C@H](O1)C(=O)O)O)O)O)O)O)C(=O)O
InChI: InChI=1S/C27H26O18/c28-9-2-1-7(3-10(9)29)13-6-12(31)15-11(30)4-8(5-14(15)42-13)41-27-23(19(35)18(34)22(44-27)25(39)40)45-26-20(36)16(32)17(33)21(43-26)24(37)38/h1-6,16-23,26-30,32-36H,(H,37,38)(H,39,40)/t16-,17-,18-,19-,20+,21-,22-,23+,26-,27+/m0/s1

描述信息

Luteolin-7-O-[beta-D-glucuronosyl-(1->2)-beta-D-glucuronide] is the glycosyloxyflavone resulting from the condensation of the hydroxy group at position 7 of luteolin with the 1 position of 2-O-beta-D-glucopyranuronosyl-beta-D-glucopyranosiduronic acid. It is a trihydroxyflavone, a glycosyloxyflavone, a dicarboxylic acid, a disaccharide derivative and a luteolin O-glucuronoside. It is a conjugate acid of a luteolin 7-O-[(beta-D-glucosiduronate)-(1->2)-(beta-D-glucosiduronate)].
luteolin-7-O-[beta-D-glucuronosyl-(1->2)-beta-D-glucuronide] is a natural product found in Elodea canadensis, Medicago truncatula, and other organisms with data available.
This compound belongs to the family of Flavonoid O-Glycosides. These are compounds containing a carbohydrate moiety which is o-glycosidically linked to one of the flavonoid backbones (2-phenylchromen-4-one, 3-phenylchromen-4-one or 4-phenylcoumarin).
The glycosyloxyflavone resulting from the condensation of the hydroxy group at position 7 of luteolin with the 1 position of 2-O-beta-D-glucopyranuronosyl-beta-D-glucopyranosiduronic acid.
Luteolin 7-diglucuronide is the major flavonoid isolated from Aloysia triphylla and Verbena officinalis[1].

同义名列表

21 个代谢物同义名

(2S,3S,4S,5R,6R)-6-(((2S,3R,4S,5S,6S)-6-Carboxy-2-((2-(3,4-dihydroxyphenyl)-5-hydroxy-4-oxo-4H-chromen-7-yl)oxy)-4,5-dihydroxytetrahydro-2H-pyran-3-yl)oxy)-3,4,5-trihydroxytetrahydro-2H-pyran-2-carboxylic acid; (2S,3S,4S,5R,6R)-6-[(2S,3R,4S,5S,6S)-6-carboxy-2-[2-(3,4-dihydroxyphenyl)-5-hydroxy-4-oxochromen-7-yl]oxy-4,5-dihydroxyoxan-3-yl]oxy-3,4,5-trihydroxyoxane-2-carboxylic acid; Luteolin 7-O-[beta-D-glucuronosyl-(1->2)-beta-D-glucuronide]; luteolin-7-O-[beta-D-glucuronosyl-(1->2)-beta-D-glucuronide]; luteolin-7-O-[beta-glucuronosyl-(1->2)-beta-glucuronide]; Luteolin 7-O-[b-D-glucuronosyl-(1->2)-b-D-glucuronide]; Luteolin 7-O-[β-D-glucuronosyl-(1->2)-β-D-glucuronide]; Luteolin-7-O-[β-D-glucuronosyl-(1->2)-β-D-glucuronide]; Luteolin-7-O-[b-D-glucuronosyl-(1->2)-b-D-glucuronide]; luteolin-7-O-(beta-glucuronyl-1-2-beta-glucuronide); Luteolin-7-O-[β-glucuronosyl-(1->2)-β-glucuronide]; Luteolin-7-O-[b-glucuronosyl-(1->2)-b-glucuronide]; luteolin 7-O-(glucuronosyl-1-2-glucuronide); Luteolin 7-O-beta-D-diglucuronide; Luteolin 7-O-β-D-diglucuronide; Luteolin 7-O-b-D-diglucuronide; Luteolin 7-glucuronosyl-(1-; luteolin-7-diglucuronide; Luteolin 7-diglucuronide; 2)-glucuronide; C27H26O18



数据库引用编号

15 个数据库交叉引用编号

分类词条

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代谢反应

0 个相关的代谢反应过程信息。

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2 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

  • Bing-Bing Ning, Yong Zhang, Dan-Dan Wu, Jin-Gang Cui, Li Liu, Pei-Wei Wang, Wen-Jian Wang, Wei-Liang Zhu, Yu Chen, Teng Zhang. Luteolin-7-diglucuronide attenuates isoproterenol-induced myocardial injury and fibrosis in mice. Acta pharmacologica Sinica. 2017 Mar; 38(3):331-341. doi: 10.1038/aps.2016.142. [PMID: 28112175]
  • M Klein, E Martinoia, G Hoffmann-Thoma, G Weissenböck. A membrane-potential dependent ABC-like transporter mediates the vacuolar uptake of rye flavone glucuronides: regulation of glucuronide uptake by glutathione and its conjugates. The Plant journal : for cell and molecular biology. 2000 Feb; 21(3):289-304. doi: 10.1046/j.1365-313x.2000.00684.x. [PMID: 10758480]
  • A Carnat, A P Carnat, O Chavignon, A Heitz, R Wylde, J L Lamaison. Luteolin 7-diglucuronide, the major flavonoid compound from Aloysia triphylla and Verbena officinalis. Planta medica. 1995 Oct; 61(5):490. doi: 10.1055/s-2006-958152. [PMID: 7480218]