luteolin 3-glucuronide (BioDeep_00000230283)

 

Secondary id: BioDeep_00000266608

PANOMIX_OTCML-2023


代谢物信息卡片


(2S,3S,4S,5R,6S)-6-(5-(5,7-dihydroxy-4-oxo-4H-chromen-2-yl)-2-hydroxyphenoxy)-3,4,5-trihydroxytetrahydro-2H-pyran-2-carboxylic acid

化学式: C21H18O12 (462.0798228)
中文名称: 木犀草素-3'-葡萄糖醛酸苷
谱图信息: 最多检出来源 Astragalus membranaceus(otcml) 35.71%

Reviewed

Last reviewed on 2024-08-14.

Cite this Page

luteolin 3-glucuronide. BioDeep Database v3. PANOMIX ltd, a top metabolomics service provider from China. https://query.biodeep.cn/s/luteolin_3-glucuronide (retrieved 2024-11-22) (BioDeep RN: BioDeep_00000230283). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).

分子结构信息

SMILES: C1(O)=CC2OC(C3C=C(O[C@H]4[C@H](O)[C@@H](O)[C@H](O)[C@@H](C(=O)O)O4)C(O)=CC=3)=CC(=O)C=2C(O)=C1
InChI: InChI=1S/C21H18O12/c22-8-4-10(24)15-11(25)6-12(31-14(15)5-8)7-1-2-9(23)13(3-7)32-21-18(28)16(26)17(27)19(33-21)20(29)30/h1-6,16-19,21-24,26-28H,(H,29,30)/t16-,17-,18+,19-,21+/m0/s1

描述信息

Luteolin 3-O-glucuronide is a luteolin glucosiduronic acid consisting of luteolin having a beta-D-glucosiduronic acid residue attached at the 3-position. It has a role as a metabolite. It is a luteolin O-glucuronoside and a trihydroxyflavone.
Luteolin 3-o-glucuronide is a natural product found in Salvia, Salvia officinalis, and other organisms with data available.
See also: Rosemary (part of).
A luteolin glucosiduronic acid consisting of luteolin having a beta-D-glucosiduronic acid residue attached at the 3-position.
Luteolin-3-O-beta-D-glucuronide is a luteolin glucosiduronic acid consisting of luteolin having a beta-D-glucosiduronic acid residue attached at the 3'-position.
Luteolin-3-O-beta-D-glucuronide is a luteolin glucosiduronic acid consisting of luteolin having a beta-D-glucosiduronic acid residue attached at the 3'-position.

同义名列表

19 个代谢物同义名

(2S,3S,4S,5R,6S)-6-(5-(5,7-dihydroxy-4-oxo-4H-chromen-2-yl)-2-hydroxyphenoxy)-3,4,5-trihydroxytetrahydro-2H-pyran-2-carboxylic acid; (2S,3S,4S,5R,6S)-6-[5-(5,7-dihydroxy-4-oxo-4H-chromen-2-yl)-2-hydroxyphenoxy]-3,4,5-trihydroxyoxane-2-carboxylic acid; (2S,3S,4S,5R,6S)-6-[5-(5,7-dihydroxy-4-oxochromen-2-yl)-2-hydroxyphenoxy]-3,4,5-trihydroxyoxane-2-carboxylic acid; .BETA.-D-GLUCOPYRANOSIDURONIC ACID, 5-(5,7-DIHYDROXY-4-OXO-4H-1-BENZOPYRAN-2-YL)-2-HYDROXYPHENYL; beta-D-Glucopyranosiduronic acid, 5-(5,7-dihydroxy-4-oxo-4H-1-benzopyran-2-yl)-2-hydroxyphenyl; 5-(5,7-dihydroxy-4-oxo-4H-chromen-2-yl)-2-hydroxyphenyl beta-D-glucopyranosiduronic acid; Luteolin 3-o-glucuronide (constituent of rosemary) [DSC]; Luteolin 3-o-glucuronide (constituent of rosemary); luteolin 3-O-beta-D-glucopyranosiduronic acid; luteolin 3-O-beta-D-glucoronopyranoside; LUTEOLIN 3-O-.BETA.-D-GLUCURONIDE; Luteolin-3-O-beta-D-glucuronide; luteolin 3-O-beta-D-glucuronide; Luteolin-3'-D-glucuronide; Luteolin-3-D-glucuronide; Luteolin 3-o-glucuronide; luteolin 3-glucuronide; UNII-1T6AU6J856; 1T6AU6J856



数据库引用编号

8 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)

4 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

  • Hui Zhi, Yuan Yuan, Chunzhen Zhang, Yiguo Jiang, Hongjian Zhang, Cheng Wang, Jianqing Ruan. Importance of OATP1B1 and 1B3 in the Liver Uptake of Luteolin and Its Consequent Glucuronidation Metabolites. Journal of agricultural and food chemistry. 2020 Feb; 68(7):2063-2070. doi: 10.1021/acs.jafc.9b06954. [PMID: 32009392]
  • Ayako Kure, Kiyotaka Nakagawa, Momoko Kondo, Shunji Kato, Fumiko Kimura, Akio Watanabe, Naoki Shoji, Sakiko Hatanaka, Tojiro Tsushida, Teruo Miyazawa. Metabolic Fate of Luteolin in Rats: Its Relationship to Anti-inflammatory Effect. Journal of agricultural and food chemistry. 2016 Jun; 64(21):4246-54. doi: 10.1021/acs.jafc.6b00964. [PMID: 27170112]
  • Yashodharan Kumarasamy, Lutfun Nahar, Maureen Byres, Abbas Delazar, Satyajit D Sarker. The assessment of biological activities associated with the major constituents of the methanol extract of 'wild carrot' (Daucus carota L) seeds. Journal of herbal pharmacotherapy. 2005; 5(1):61-72. doi: ". [PMID: 16093236]
  • A Heitz, A Carnat, D Fraisse, A P Carnat, J L Lamaison. Luteolin 3'-glucuronide, the major flavonoid from Melissa officinalis subsp. officinalis. Fitoterapia. 2000 Apr; 71(2):201-2. doi: 10.1016/s0367-326x(99)00118-5. [PMID: 10727822]