Glycyrrhisoflavone (BioDeep_00000255068)

   

PANOMIX_OTCML-2023


代谢物信息卡片


3-[3-(3-methylbut-2-enyl)-4,5-bis(oxidanyl)phenyl]-5,7-bis(oxidanyl)chromen-4-one

化学式: C20H18O6 (354.1103328)
中文名称: 西北甘草异黄酮
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: c12c(c(=O)c(co1)c1cc(c(c(c1)O)O)CC=C(C)C)c(cc(c2)O)O
InChI: InChI=1S/C20H18O6/c1-10(2)3-4-11-5-12(6-16(23)19(11)24)14-9-26-17-8-13(21)7-15(22)18(17)20(14)25/h3,5-9,21-24H,4H2,1-2H3

描述信息

Glycyrrhisoflavone is a natural product found in Psorothamnus arborescens, Psorothamnus arborescens var. minutifolius, and other organisms with data available.
Glycyrrhisoflavone, an active prenylflavonoid, inhibits α-glucosidase[1].
Glycyrrhisoflavone, an active prenylflavonoid, inhibits α-glucosidase[1].

同义名列表

6 个代谢物同义名

3-[3-(3-methylbut-2-enyl)-4,5-bis(oxidanyl)phenyl]-5,7-bis(oxidanyl)chromen-4-one; 3-[3,4-dihydroxy-5-(3-methylbut-2-enyl)phenyl]-5,7-dihydroxy-chromen-4-one; 3-[3,4-dihydroxy-5-(3-methylbut-2-enyl)phenyl]-5,7-dihydroxychromen-4-one; 5/-(3-Methyl-2-butenyl)-3/,4/,5,7-tetrahydroxyisoflavone; Glycyrrhisoflavone; JN0



数据库引用编号

5 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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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)

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。
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文献列表

  • Yan Lin, Yi Kuang, Kai Li, Shuang Wang, Shuai Ji, Kuan Chen, Wei Song, Xue Qiao, Min Ye. Nrf2 activators from Glycyrrhiza inflata and their hepatoprotective activities against CCl4-induced liver injury in mice. Bioorganic & medicinal chemistry. 2017 10; 25(20):5522-5530. doi: 10.1016/j.bmc.2017.08.018. [PMID: 28835349]
  • Yan Lin, Yi Kuang, Kai Li, Shuang Wang, Wei Song, Xue Qiao, Gulnar Sabir, Min Ye. Screening for bioactive natural products from a 67-compound library of Glycyrrhiza inflata. Bioorganic & medicinal chemistry. 2017 07; 25(14):3706-3713. doi: 10.1016/j.bmc.2017.05.009. [PMID: 28522265]
  • Takashi Matsui, Subehan Lallo, Khoirun Nisa, Hiroyuki Morita. Filamenting temperature-sensitive mutant Z inhibitors from Glycyrrhiza glabra and their inhibitory mode of action. Bioorganic & medicinal chemistry letters. 2017 03; 27(6):1420-1424. doi: 10.1016/j.bmcl.2017.01.095. [PMID: 28196701]
  • Songpei Li, Wei Li, Yinghua Wang, Yoshihisa Asada, Kazuo Koike. Prenylflavonoids from Glycyrrhiza uralensis and their protein tyrosine phosphatase-1B inhibitory activities. Bioorganic & medicinal chemistry letters. 2010 Sep; 20(18):5398-401. doi: 10.1016/j.bmcl.2010.07.110. [PMID: 20724155]
  • Manar M Salem, Karl A Werbovetz. Isoflavonoids and other compounds from Psorothamnus arborescens with antiprotozoal activities. Journal of natural products. 2006 Jan; 69(1):43-9. doi: 10.1021/np0502600. [PMID: 16441066]
  • K Fukuchi, H Sakagami, T Okuda, T Hatano, S Tanuma, K Kitajima, Y Inoue, S Inoue, S Ichikawa, M Nonoyama. Inhibition of herpes simplex virus infection by tannins and related compounds. Antiviral research. 1989 Jun; 11(5-6):285-97. doi: 10.1016/0166-3542(89)90038-7. [PMID: 2552915]