5-Hydroxyauranetin (BioDeep_00000025411)

 

Secondary id: BioDeep_00000270303

human metabolite PANOMIX_OTCML-2023


代谢物信息卡片


5-Hydroxy-3,6,7,8-tetramethoxy-2-(4-methoxyphenyl)-4H-1-Benzopyran-4-one

化学式: C20H20O8 (388.115812)
中文名称:
谱图信息: 最多检出来源 Astragalus membranaceus(otcml) 20%

分子结构信息

SMILES: c1(c(c(c2c(c1OC)oc(c(c2=O)OC)c1ccc(cc1)OC)O)OC)OC
InChI: InChI=1S/C20H20O8/c1-23-11-8-6-10(7-9-11)15-17(24-2)13(21)12-14(22)18(25-3)20(27-5)19(26-4)16(12)28-15/h6-9,22H,1-5H3

描述信息

5-Hydroxyauranetin is found in citrus. 5-Hydroxyauranetin is a constituent of Citrus aurantium (Seville orange).
Constituent of Citrus aurantium (Seville orange). 5-Hydroxyauranetin is found in citrus.

同义名列表

6 个代谢物同义名

5-Hydroxy-3,6,7,8-tetramethoxy-2-(4-methoxyphenyl)-4H-1-Benzopyran-4-one; 5-hydroxy-3,6,7,8-tetramethoxy-2-(4-methoxyphenyl)-4H-chromen-4-one; 5-Hydroxy-3,4,6,7,8-pentamethoxyflavone; 5-Hydroxy-3,6,7,8,4-pentamethoxyflavone; 4-O-Methylcalycopterin; 5-Hydroxyauranetin



数据库引用编号

9 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)

9 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

  • Priscila de Souza, Thaise Boeing, Lincon Bordignon Somensi, Camile Cecconi Cechinel-Zanchett, Jairo Kenupp Bastos, Marcel Petreanu, Rivaldo Niero, Valdir Cechinel-Filho, Luisa Mota da Silva, Sérgio Faloni de Andrade. Diuretic effect of extracts, fractions and two compounds 2α,3β,19α-trihydroxy-urs-12-en-28-oic acid and 5-hydroxy-3,6,7,8,4'-pentamethoxyflavone from Rubus rosaefolius Sm. (Rosaceae) leaves in rats. Naunyn-Schmiedeberg's archives of pharmacology. 2017 Apr; 390(4):351-360. doi: 10.1007/s00210-016-1333-4. [PMID: 28013356]
  • Qun Sun, Ye Lu, Shuang-Qing Wu, Shi Yao, Jian Zhang. [Study on the chemical constituents from Gnaphalium hypoleucum]. Zhong yao cai = Zhongyaocai = Journal of Chinese medicinal materials. 2012 Apr; 35(4):566-8. doi: ". [PMID: 23019902]
  • Guy Lewin, Narayan Bhat Shridhar, Geneviève Aubert, Sylviane Thoret, Joëlle Dubois, Thierry Cresteil. Synthesis of antiproliferative flavones from calycopterin, major flavonoid of Calycopteris floribunda Lamk. Bioorganic & medicinal chemistry. 2011 Jan; 19(1):186-96. doi: 10.1016/j.bmc.2010.11.035. [PMID: 21146994]
  • Georgina N Diaz Napal, María C Carpinella, Sara M Palacios. Antifeedant activity of ethanolic extract from Flourensia oolepis and isolation of pinocembrin as its active principle compound. Bioresource technology. 2009 Jul; 100(14):3669-73. doi: 10.1016/j.biortech.2009.02.050. [PMID: 19342224]
  • M Morimoto, S Kumeda, K Komai. Insect antifeedant flavonoids from Gnaphalium affine D. Don. Journal of agricultural and food chemistry. 2000 May; 48(5):1888-91. doi: 10.1021/jf990282q. [PMID: 10820110]
  • D G Kingston, M M Rao, W V Zucker. Plant anticancer agents. IX. Constituents of Hyptis tomentosa. Journal of natural products. 1979 Sep; 42(5):496-9. doi: 10.1021/np50005a010. [PMID: 521819]