Demethylsuberosin (BioDeep_00001867496)

Main id: BioDeep_00000000396

 

PANOMIX_OTCML-2023 natural product


代谢物信息卡片


2H-1-Benzopyran-2-one, 7-hydroxy-6-(3-methyl-2-buten-1-yl)-

化学式: C14H14O3 (230.0942894)
中文名称: 7-去甲基软木花椒素, 去甲软木花椒素, 去甲基软木花椒素
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: CC(=CCC1=C(C=C2C(=C1)C=CC(=O)O2)O)C
InChI: InChI=1S/C14H14O3/c1-9(2)3-4-10-7-11-5-6-14(16)17-13(11)8-12(10)15/h3,5-8,15H,4H2,1-2H3

描述信息

7-demethylsuberosin is a hydroxycoumarin that is 7-hydroxycoumarin which is substituted at position 6 by a 3-methylbut-2-en-1-yl group. A natural product found in Citropsis articulata. It has a role as a plant metabolite.
Demethylsuberosin is a natural product found in Prangos tschimganica, Limonia acidissima, and other organisms with data available.
A hydroxycoumarin that is 7-hydroxycoumarin which is substituted at position 6 by a 3-methylbut-2-en-1-yl group. A natural product found in Citropsis articulata.
D011838 - Radiation-Sensitizing Agents > D017319 - Photosensitizing Agents > D011564 - Furocoumarins
Demethylsuberosin (7-Demethylsuberosin) is a coumarin compound isolated from Angelica gigas Nakai, and has anti-inflammatory activity[1].
Demethylsuberosin (7-Demethylsuberosin) is a coumarin compound isolated from Angelica gigas Nakai, and has anti-inflammatory activity[1].

同义名列表

19 个代谢物同义名

2H-1-Benzopyran-2-one, 7-hydroxy-6-(3-methyl-2-buten-1-yl)-; 2H-1-Benzopyran-2-one,7-hydroxy-6-(3-methyl-2-buten-1-yl)-; 7-HYDROXY-6-(3-METHYL-2-BUTEN-1-YL)-2H-1-BENZOPYRAN-2-ONE; 2H-1-Benzopyran-2-one, 7-hydroxy-6-(3-methyl-2-butenyl)-; 7-hydroxy-6-(3-methylbut-2-en-1-yl)-2H-chromen-2-one; 7-hydroxy-6-(3-methylbut-2-enyl)chromen-2-one; COUMARIN, 7-HYDROXY-6-(3-METHYL-2-BUTENYL)-; 6-(3,3-dimethylallyl)-7-hydroxycoumarin; 7-hydroxy-6-prenyl-1-benzopyran-2-one; 6-(DIMETHYLALLYL)UMBELLIFERONE; 7-hydroxy-6-prenylcoumarin; 7-demethylsuberosine; 7-Demethylsuberosin; Demethylsuberosin; UNII-SDM71QIW25; MEGxp0_001461; SDM71QIW25; Demethylsuberosin; Demethylsuberosin



数据库引用编号

15 个数据库交叉引用编号

分类词条

相关代谢途径

Reactome(0)

BioCyc(1)

PlantCyc(1)

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)

67 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

  • Jaeyoung Kwon, Nguyen Tuan Hiep, Dong-Woo Kim, Sungeun Hong, Yuanqiang Guo, Bang Yeon Hwang, Hak Ju Lee, Woongchon Mar, Dongho Lee. Chemical Constituents Isolated from the Root Bark of Cudrania tricuspidata and Their Potential Neuroprotective Effects. Journal of natural products. 2016 08; 79(8):1938-51. doi: 10.1021/acs.jnatprod.6b00204. [PMID: 27420919]
  • Guo-jiao Kang, Shu-juan Yang, Hai-yu Zhou, Zeng-ming Yang, Ling-yun Chen. [Chemical constituents of pattra medicine Euodia lepta]. Zhong yao cai = Zhongyaocai = Journal of Chinese medicinal materials. 2014 Jan; 37(1):74-6. doi: . [PMID: 25090710]
  • Damien Lacroix, Soizic Prado, Dennis Kamoga, John Kasenene, Bernard Bodo. Structure and in vitro antiparasitic activity of constituents of Citropsis articulata root bark. Journal of natural products. 2011 Oct; 74(10):2286-9. doi: 10.1021/np2004825. [PMID: 21985060]
  • S Y Kang, K Y Lee, S H Sung, M J Park, Y C Kim. Coumarins isolated from Angelica gigas inhibit acetylcholinesterase: structure-activity relationships. Journal of natural products. 2001 May; 64(5):683-5. doi: 10.1021/np000441w. [PMID: 11374978]
  • . . . . doi: . [PMID: 17068340]