luteolin-7-glucuronide (BioDeep_00001103551)

   


代谢物信息卡片


luteolin-7-glucuronide

化学式: C21H18O12 (462.0798228)
中文名称:
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O)O
InChI: InChI=1S/C21H18O12/c22-9-2-1-7(3-10(9)23)13-6-12(25)15-11(24)4-8(5-14(15)32-13)31-21-18(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

同义名列表

1 个代谢物同义名

luteolin-7-glucuronide



数据库引用编号

1 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)

0 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

  • Sung Woo Jeong, Semin Park, Jong Sung Jin, On Nuri Seo, Gon-Sup Kim, Yun-Hi Kim, Hanhong Bae, Gyemin Lee, Soo Taek Kim, Won Sup Lee, Sung Chul Shin. Influences of four different light-emitting diode lights on flowering and polyphenol variations in the leaves of chrysanthemum (Chrysanthemum morifolium). Journal of agricultural and food chemistry. 2012 Oct; 60(39):9793-800. doi: 10.1021/jf302272x. [PMID: 22970652]
  • Hong-Li Liu, Bai-Lian Liu, Guo-Cai Wang, Yi Dai, Wen-Cai Ye, Yao-Lan Li. [Studies on the chemical constituents from Conyza canadensis]. Zhong yao cai = Zhongyaocai = Journal of Chinese medicinal materials. 2011 May; 34(5):718-20. doi: . [PMID: 21954558]
  • Kyoung-Sook Kim, Yeon-Joo Kwak, Kyung-Mi Kim, Hai Yang Yu, Byoung-Won Kang, Eunsook Chung, Young-Choon Lee, Jung-In Kim, Jai-Heon Lee. Purification and structure determination of gelatinase and collagenase inhibitors from Viola patrinii fermentation extracts. Immunopharmacology and immunotoxicology. 2010 Dec; 32(4):614-6. doi: 10.3109/08923971003645631. [PMID: 20196628]
  • B Benedek, N Geisz, W Jäger, T Thalhammer, B Kopp. Choleretic effects of yarrow (Achillea millefolium s.l.) in the isolated perfused rat liver. Phytomedicine : international journal of phytotherapy and phytopharmacology. 2006 Nov; 13(9-10):702-6. doi: 10.1016/j.phymed.2005.10.005. [PMID: 16303291]
  • Irene Parejo, Elisabetta Caprai, Jaume Bastida, Francesc Viladomat, Olga Jáuregui, Carles Codina. Investigation of Lepechinia graveolens for its antioxidant activity and phenolic composition. Journal of ethnopharmacology. 2004 Sep; 94(1):175-84. doi: 10.1016/j.jep.2004.05.017. [PMID: 15261980]
  • Gerd Vanhoenacker, Philippe Van Rompaey, Denis De Keukeleire, Pat Sandra. Chemotaxonomic features associated with flavonoids of cannabinoid-free cannabis (Cannabis sativa subsp. sativa L.) in relation to hops (Humulus lupulus L.). Natural product letters. 2002 Feb; 16(1):57-63. doi: 10.1080/1057563029001/4863. [PMID: 11942684]
  • H G Gumbinger, H Winterhoff, R Wylde, A Sosa. On the influence of the sugar moiety on the antigonadotropic activity of luteoline glycosides. Planta medica. 1992 Feb; 58(1):49-50. doi: 10.1055/s-2006-961388. [PMID: 1620743]