Kuraridinol (BioDeep_00000011704)

   

PANOMIX_OTCML-2023


代谢物信息卡片


(2E) -1- [ 2,4-Dihydroxy-3- [ 5-hydroxy-5-methyl-2- (1-methylethenyl) hexyl ] -6-methoxyphenyl ] -3- (2,4-dihydroxyphenyl) -2-propen-1-one

化学式: C26H32O7 (456.2147922)
中文名称:
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: C1=CC(O)=CC(O)=C1/C=C/C(=O)C1C(O)=C(CC(C(=C)C)CCC(O)(C)C)C(O)=CC=1OC
InChI: InChI=1S/C26H32O7/c1-15(2)17(10-11-26(3,4)32)12-19-22(30)14-23(33-5)24(25(19)31)20(28)9-7-16-6-8-18(27)13-21(16)29/h6-9,13-14,17,27,29-32H,1,10-12H2,2-5H3/b9-7+

描述信息

A member of the class of chalcones that is trans-chalcone substituted by hydroxy groups at positions 2, 4, 2 and 4, a methoxy group at position 6 and a 5-hydroxy-5-methyl-2-(prop-1-en-2-yl)hexyl group at position 3 respectively.

同义名列表

2 个代谢物同义名

Kuraridinol; (2E) -1- [ 2,4-Dihydroxy-3- [ 5-hydroxy-5-methyl-2- (1-methylethenyl) hexyl ] -6-methoxyphenyl ] -3- (2,4-dihydroxyphenyl) -2-propen-1-one



数据库引用编号

14 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)

8 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

  • Hyun Ah Jung, Da-Mi Jeong, Hae Young Chung, Hyun Ae Lim, Ji Young Kim, Na Young Yoon, Jae Sue Choi. Re-evaluation of the antioxidant prenylated flavonoids from the roots of Sophora flavescens. Biological & pharmaceutical bulletin. 2008 May; 31(5):908-15. doi: 10.1248/bpb.31.908. [PMID: 18451517]
  • Hyun Young Kim, Da Mi Jeong, Hee Jin Jung, Yu Jung Jung, Takako Yokozawa, Jae Sue Choi. Hypolipidemic effects of Sophora flavescens and its constituents in poloxamer 407-induced hyperlipidemic and cholesterol-fed rats. Biological & pharmaceutical bulletin. 2008 Jan; 31(1):73-8. doi: 10.1248/bpb.31.73. [PMID: 18175945]
  • Sook Kyung Hyun, Won-Hee Lee, Da Mi Jeong, Youngsoo Kim, Jae Sue Choi. Inhibitory effects of kurarinol, kuraridinol, and trifolirhizin from Sophora flavescens on tyrosinase and melanin synthesis. Biological & pharmaceutical bulletin. 2008 Jan; 31(1):154-8. doi: 10.1248/bpb.31.154. [PMID: 18175961]
  • Lei Zhang, Liang Xu, Shan-Shan Xiao, Qiong-Feng Liao, Qing Li, Jian Liang, Xiao-Hui Chen, Kai-Shun Bi. Characterization of flavonoids in the extract of Sophora flavescens Ait. by high-performance liquid chromatography coupled with diode-array detector and electrospray ionization mass spectrometry. Journal of pharmaceutical and biomedical analysis. 2007 Sep; 44(5):1019-28. doi: 10.1016/j.jpba.2007.04.019. [PMID: 17658714]
  • Mee Jung Jung, Sam Sik Kang, Hyun Ah Jung, Goon Ja Kim, Jae Sue Choi. Isolation of flavonoids and a cerebroside from the stem bark of Albizzia julibrissin. Archives of pharmacal research. 2004 Jun; 27(6):593-9. doi: 10.1007/bf02980155. [PMID: 15283458]