Luteollin5-glucoside (BioDeep_00000230251)

Main id: BioDeep_00000240910

 

PANOMIX_OTCML-2023


代谢物信息卡片


2-(3,4-dihydroxyphenyl)-7-hydroxy-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydropyran-2-yl]oxy-chromen-4-one

化学式: C21H20O11 (448.100557)
中文名称: 木犀草素-5-O-葡萄糖苷
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: C1(O)=CC2OC(C3C=C(O)C(O)=CC=3)=CC(=O)C=2C(O[C@H]2[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O2)=C1
InChI: InChI=1S/C21H20O11/c22-7-16-18(27)19(28)20(29)21(32-16)31-15-5-9(23)4-14-17(15)12(26)6-13(30-14)8-1-2-10(24)11(25)3-8/h1-6,16,18-25,27-29H,7H2/t16-,18-,19+,20-,21-/m1/s1

描述信息

Luteolin 5-glucoside is a natural product found in Verbascum lychnitis, Gentiana arisanensis, and other organisms with data available.
Luteolin 5-O-glucoside, a major flavonoidfrom Cirsium maackii, possesses anti-inflammatory activity. Luteolin 5-O-glucoside inhibits LPS-induced NO production and t-BHP-induced ROS generation. Luteolin 5-O-glucoside suppresses the expression of iNOS and COX-2 in macrophages[1].
Luteolin 5-O-glucoside, a major flavonoidfrom Cirsium maackii, possesses anti-inflammatory activity. Luteolin 5-O-glucoside inhibits LPS-induced NO production and t-BHP-induced ROS generation. Luteolin 5-O-glucoside suppresses the expression of iNOS and COX-2 in macrophages[1].

同义名列表

18 个代谢物同义名

2-(3,4-dihydroxyphenyl)-7-hydroxy-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydropyran-2-yl]oxy-chromen-4-one; 2-(3,4-dihydroxyphenyl)-7-hydroxy-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one; 4H-1-Benzopyran-4-one, 2-(3,4-dihydroxyphenyl)-5-(.beta.-D-glucopyranosyloxy)-7-hydroxy-; 4H-1-Benzopyran-4-one, 2-(3,4-dihydroxyphenyl)-5-(beta-D-glucopyranosyloxy)-7-hydroxy-; 2-(3,4-Dihydroxyphenyl)-7-hydroxy-4-oxo-4H-1-benzopyran-5-yl hexopyranoside; LUTEOLIN 5-O-.BETA.-D-GLUCOPYRANOSIDE; luteolin-5-o-beta-d-glucopyranoside; Luteolin-5-O-beta-D-glucoside; Luteolin-5-O-glucopyranoside; luteolin 5-O-glucopyranoside; LUTEOLIN 5-GLUCOSIDE [MI]; Luteolin 5-O-glucoside; Luteolin-5-O-glucoside; Luteollin 5-glucoside; Luteollin5-glucoside; Luteolin 5-glucoside; UNII-CNI9E8ORF6; CNI9E8ORF6



数据库引用编号

6 个数据库交叉引用编号

分类词条

相关代谢途径

Reactome(0)

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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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BioCyc(0)

WikiPathways(0)

Plant Reactome(0)

INOH(0)

PlantCyc(0)

COVID-19 Disease Map(0)

PathBank(0)

PharmGKB(0)

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

  • Ophélie Fadel, Luc Girard, Donatien Gomes Rodrigues, Pierre Bauduin, Xavier Le Goff, Anne Rossignol-Castera, Annabelle L'Hermitte, Olivier Diat. Micellization in vegetable oils: A structural characterisation. Colloids and surfaces. B, Biointerfaces. 2017 Jun; 154(?):279-286. doi: 10.1016/j.colsurfb.2017.03.025. [PMID: 28351800]
  • Handan Gokben Sevindik, Ufuk Ozgen, Alptug Atila, Handan Ozturk Er, Cavit Kazaz, Hayri Duman. Phtytochemical Studies and Quantitative HPLC Analysis of Rosmarinic Acid and Luteolin 5-O-β-D-Glucopyranoside on Thymus praecox subsp. grossheimii var. grossheimii. Chemical & pharmaceutical bulletin. 2015; 63(9):720-5. doi: 10.1248/cpb.c14-00877. [PMID: 26329865]
  • Hyun Ah Jung, Seong Eun Jin, Byung-Sun Min, Byung-Woo Kim, Jae Sue Choi. Anti-inflammatory activity of Korean thistle Cirsium maackii and its major flavonoid, luteolin 5-O-glucoside. Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association. 2012 Jun; 50(6):2171-9. doi: 10.1016/j.fct.2012.04.011. [PMID: 22525859]
  • Hyun Ah Jung, Yeong Shik Kim, Jae Sue Choi. Quantitative HPLC analysis of two key flavonoids and inhibitory activities against aldose reductase from different parts of the Korean thistle, Cirsium maackii. Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association. 2009 Nov; 47(11):2790-7. doi: 10.1016/j.fct.2009.08.014. [PMID: 19733610]
  • Prasoon Gupta, Dinesh Kumar Yadav, Kiran Babu Siripurapu, Guatam Palit, Rakesh Maurya. Constituents of Ocimum sanctum with antistress activity. Journal of natural products. 2007 Sep; 70(9):1410-6. doi: 10.1021/np0700164. [PMID: 17850106]
  • Hai-yong Chen, Chang-xin Zhou, Yi-jia Lou, Zhi-hong Duan, Yu Zhao. [Chemical constituents from Elsholtzia blanda]. Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica. 2005 Oct; 30(20):1589-91. doi: . [PMID: 16422538]
  • Supinya Tewtrakul, Hirotsugu Miyashiro, Norio Nakamura, Masao Hattori, Takuya Kawahata, Toru Otake, Tomokazu Yoshinaga, Tamio Fujiwara, Tanomjit Supavita, Supreeya Yuenyongsawad, Pranee Rattanasuwon, Sukanya Dej-Adisai. HIV-1 integrase inhibitory substances from Coleus parvifolius. Phytotherapy research : PTR. 2003 Mar; 17(3):232-9. doi: 10.1002/ptr.1111. [PMID: 12672152]