6-Hydroxyluteolin (BioDeep_00000007859)

 

Secondary id: BioDeep_00000270091, BioDeep_00000862788

human metabolite PANOMIX_OTCML-2023 natural product Volatile Flavor Compounds


代谢物信息卡片


2-(3,4-Dihydroxyphenyl)-5,6,7-trihydroxy-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 Astragalus membranaceus(otcml) 8%

分子结构信息

SMILES: c1(c(c(c2c(c1)oc(cc2=O)c1ccc(c(c1)O)O)O)O)O
InChI: InChI=1S/C15H10O7/c16-7-2-1-6(3-8(7)17)11-4-9(18)13-12(22-11)5-10(19)14(20)15(13)21/h1-5,16-17,19-21H

描述信息

Isolated from Valerianella eriocarpa (Italian corn salad). 6-Hydroxyluteolin is found in many foods, some of which are common thyme, mexican oregano, green vegetables, and lemon verbena.
6-Hydroxyluteolin is found in common thyme. 6-Hydroxyluteolin is isolated from Valerianella eriocarpa (Italian corn salad).

同义名列表

9 个代谢物同义名

2-(3,4-Dihydroxyphenyl)-5,6,7-trihydroxy-4H-1-benzopyran-4-one; 2-(3,4-Dihydroxyphenyl)-5,6,7-trihydroxy-4H-chromen-4-one; 3,4,5,6,7-Pentahydroxyflavone; 5,6,7,3,4-Pentahydroxyflavone; Demethylpedalitin; 6-Hydroxyluteolin; 6-OH-Luteolin; Nornepetin; 6-Hydroxyluteolin



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)

74 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

  • Wael A Elmasri, Tianjiao Yang, Phat Tran, Mohamed-Elamir F Hegazy, Abdul N Hamood, Yehia Mechref, Paul W Paré. Teucrium polium phenylethanol and iridoid glycoside characterization and flavonoid inhibition of biofilm-forming Staphylococcus aureus. Journal of natural products. 2015 Jan; 78(1):2-9. doi: 10.1021/np5004092. [PMID: 25524452]
  • Kaan Polatoğlu, Omer Cem Karakoç, Fatih Demirci, Ayhan Gökçe, Nezhun Gören. Chemistry and biological activities of Tanacetum chiliophyllum var. oligocephalum extracts. Journal of AOAC International. 2013 Nov; 96(6):1222-7. doi: 10.5740/jaoacint.sgepolatoglu. [PMID: 24645497]
  • Cristiano Soleo Funari, Thais Gaban Passalacqua, Daniel Rinaldo, Assunta Napolitano, Michela Festa, Anna Capasso, Sonia Piacente, Cosimo Pizza, Maria Claudia Marx Young, Giselda Durigan, Dulce Helena Siqueira Silva. Interconverting flavanone glucosides and other phenolic compounds in Lippia salviaefolia Cham. ethanol extracts. Phytochemistry. 2011 Nov; 72(16):2052-61. doi: 10.1016/j.phytochem.2011.07.004. [PMID: 21871644]
  • Nan Qin, Chun-Bao Li, Mei-Na Jin, Li-Huan Shi, Hong-Quan Duan, Wen-Yan Niu. Synthesis and biological activity of novel tiliroside derivants. European journal of medicinal chemistry. 2011 Oct; 46(10):5189-95. doi: 10.1016/j.ejmech.2011.07.059. [PMID: 21856048]
  • 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]
  • Yanhui Meng, Amanda J Krzysiak, Michael J Durako, Jennifer I Kunzelman, Jeffrey L C Wright. Flavones and flavone glycosides from Halophila johnsonii. Phytochemistry. 2008 Oct; 69(14):2603-8. doi: 10.1016/j.phytochem.2008.07.007. [PMID: 18771781]
  • 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]
  • Nour-Eddine Es-Safi, Samira Khlifi, Lucien Kerhoas, Albert Kollmann, Ahmed El Abbouyi, Paul-Henri Ducrot. Antioxidant constituents of the aerial parts of Globularia alypum growing in Morocco. Journal of natural products. 2005 Aug; 68(8):1293-6. doi: 10.1021/np0501233. [PMID: 16124783]
  • Dirk C Albach, Renée J Grayer, Søren Rosendal Jensen, Fevzi Ozgökce, Nigel C Veitch. Acylated flavone glycosides from Veronica. Phytochemistry. 2003 Dec; 64(7):1295-301. doi: 10.1016/j.phytochem.2003.08.012. [PMID: 14599528]
  • Zhao Feng Peng, Dieter Strack, Alfred Baumert, Ramanathan Subramaniam, Ngoh Khang Goh, Tet Fatt Chia, Swee Ngin Tan, Lian Sai Chia. Antioxidant flavonoids from leaves of Polygonum hydropiper L. Phytochemistry. 2003 Jan; 62(2):219-28. doi: 10.1016/s0031-9422(02)00504-6. [PMID: 12482460]
  • Tsuneatsu Nagao, Fumiko Abe, Junei Kinjo, Hikaru Okabe. Antiproliferative constituents in plants 10. Flavones from the leaves of Lantana montevidensis Briq. and consideration of structure-activity relationship. Biological & pharmaceutical bulletin. 2002 Jul; 25(7):875-9. doi: 10.1248/bpb.25.875. [PMID: 12132661]
  • Fumiko Abe, Tsuneatsu Nagao, Hikaru Okabe. Antiproliferative constituents in plants 9. Aerial parts of Lippia dulcis and Lippia canescens. Biological & pharmaceutical bulletin. 2002 Jul; 25(7):920-2. doi: 10.1248/bpb.25.920. [PMID: 12132670]