6-Hydroxykaempferol (BioDeep_00000270328)

Main id: BioDeep_00000007855

 

PANOMIX_OTCML-2023


代谢物信息卡片


3,5,6,7-Tetrahydroxy-2- (4-hydroxyphenyl) -4H-1-benzopyran-4-one

化学式: C15H10O7 (302.042651)
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(c2c(c1)oc(c(c2=O)O)c1ccc(cc1)O)O)O)O
InChI: InChI=1S/C15H10O7/c16-7-3-1-6(2-4-7)15-14(21)13(20)10-9(22-15)5-8(17)11(18)12(10)19/h1-5,16-19,21H

描述信息

6-Hydroxykaempferol is a natural product found in Ficus virens, Eupatorium cannabinum, and other organisms with data available.

同义名列表

3 个代谢物同义名

3,5,6,7-tetrahydroxy-2-(4-hydroxyphenyl)chromen-4-one; 6-Hydroxykaempferol; 3,5,6,7-Tetrahydroxy-2- (4-hydroxyphenyl) -4H-1-benzopyran-4-one



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)

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)

3 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

  • Anil Pareek, Manish Suthar, Garvendra S Rathore, Vijay Bansal. Feverfew (Tanacetum parthenium L.): A systematic review. Pharmacognosy reviews. 2011 Jan; 5(9):103-10. doi: 10.4103/0973-7847.79105. [PMID: 22096324]
  • Wei Qu, Li Fan, Yun-chul Kim, Shizuma Ishikawa, Sanae M M Iguchi-Ariga, Xiao-Ping Pu, Hiroyoshi Ariga. Kaempferol derivatives prevent oxidative stress-induced cell death in a DJ-1-dependent manner. Journal of pharmacological sciences. 2009 Jun; 110(2):191-200. doi: 10.1254/jphs.09045fp. [PMID: 19498271]
  • Fumio Matsuda, Keiko Yonekura-Sakakibara, Rie Niida, Takashi Kuromori, Kazuo Shinozaki, Kazuki Saito. MS/MS spectral tag-based annotation of non-targeted profile of plant secondary metabolites. The Plant journal : for cell and molecular biology. 2009 Feb; 57(3):555-77. doi: 10.1111/j.1365-313x.2008.03705.x. [PMID: 18939963]
  • Hai-Jiang Zhang, Yi-Yu Cheng. An HPLC/MS method for identifying major constituents in the hypocholesterolemic extracts of Chinese medicine formula 'Xue-Fu-Zhu-Yu decoction'. Biomedical chromatography : BMC. 2006 Aug; 20(8):821-6. doi: 10.1002/bmc.607. [PMID: 16345012]
  • Joo-Heon Yoon, Seung Joon Baek. Molecular targets of dietary polyphenols with anti-inflammatory properties. Yonsei medical journal. 2005 Oct; 46(5):585-96. doi: 10.3349/ymj.2005.46.5.585. [PMID: 16259055]
  • María A Ponce, José M Scervino, Rosa Erra-Balsells, Juan A Ocampo, Alicia M Godeas. Flavonoids from shoots and roots of Trifolium repens (white clover) grown in presence or absence of the arbuscular mycorrhizal fungus Glomus intraradices. Phytochemistry. 2004 Jul; 65(13):1925-30. doi: 10.1016/j.phytochem.2004.06.005. [PMID: 15279999]
  • Christine A Williams, Jeffrey B Harborne, Jenny R Greenham, Renée J Grayer, Geoffrey C Kite, John Eagles. Variations in lipophilic and vacuolar flavonoids among European Pulicaria species. Phytochemistry. 2003 Sep; 64(1):275-83. doi: 10.1016/s0031-9422(03)00207-3. [PMID: 12946426]
  • Jenny Greenham, Jeffrey B Harborne, Christine A Williams. Identification of lipophilic flavones and flavonols by comparative HPLC, TLC and UV spectral analysis. Phytochemical analysis : PCA. 2003 Mar; 14(2):100-18. doi: 10.1002/pca.693. [PMID: 12693635]