Pinosylvin methyl ether (BioDeep_00000007990)

 

Secondary id: BioDeep_00000396531

human metabolite PANOMIX_OTCML-2023 Volatile Flavor Compounds natural product


代谢物信息卡片


3-methoxy-5-(2-phenylethenyl)phenol

化学式: C15H14O2 (226.09937440000002)
中文名称: 松油基乙烯基单甲醚, 银松素单甲醚
谱图信息: 最多检出来源 Viridiplantae(plant) 1.57%

分子结构信息

SMILES: C1=C(OC)C=C(/C=C/C2=CC=CC=C2)C=C1O
InChI: InChI=1S/C15H14O2/c1-17-15-10-13(9-14(16)11-15)8-7-12-5-3-2-4-6-12/h2-11,16H,1H3/b8-7+

描述信息

同义名列表

6 个代谢物同义名

3-methoxy-5-(2-phenylethenyl)phenol; 3-hydroxy-5-methoxystilbene; Pinosylvin monomethyl ether; Pinosylvin methyl ether; 5-Methoxy-3-stilbenol; Pinosylvin methyl ether



数据库引用编号

20 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

2 个相关的代谢反应过程信息。

Reactome(0)

BioCyc(1)

WikiPathways(0)

Plant Reactome(0)

INOH(0)

PlantCyc(1)

COVID-19 Disease Map(0)

PathBank(0)

PharmGKB(0)

219 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

  • Syuhei Nakao, Miyuki Mabuchi, Shenglan Wang, Yoko Kogure, Tadashi Shimizu, Koichi Noguchi, Akito Tanaka, Yi Dai. Synthesis of resveratrol derivatives as new analgesic drugs through desensitization of the TRPA1 receptor. Bioorganic & medicinal chemistry letters. 2017 07; 27(14):3167-3172. doi: 10.1016/j.bmcl.2017.05.025. [PMID: 28576617]
  • Xiaojia Li, Takafumi Horishita, Yumiko Toyohira, Hui Shao, Jie Bai, Haixia Bo, Xinbo Song, Shin Ishikane, Yukari Yoshinaga, Noriaki Satoh, Masato Tsutsui, Nobuyuki Yanagihara. Inhibitory effects of pine nodule extract and its component, SJ-2, on acetylcholine-induced catecholamine secretion and synthesis in bovine adrenal medullary cells. Journal of pharmacological sciences. 2017 Apr; 133(4):268-275. doi: 10.1016/j.jphs.2017.03.006. [PMID: 28433565]
  • Victor S Sobolev, Shabana I Khan, Nurhayat Tabanca, David E Wedge, Susan P Manly, Stephen J Cutler, Monique R Coy, James J Becnel, Scott A Neff, James B Gloer. Biological activity of peanut (Arachis hypogaea) phytoalexins and selected natural and synthetic Stilbenoids. Journal of agricultural and food chemistry. 2011 Mar; 59(5):1673-82. doi: 10.1021/jf104742n. [PMID: 21314127]
  • Shugeng Cao, Mohamed M Radwan, Andrew Norris, James S Miller, Fidy Ratovoson, Andrianjafy Mamisoa, Rabodo Andriantsiferana, Vincent E Rasamison, Stephan Rakotonandrasana, David G I Kingston. Cytotoxic and other compounds from Didymochlaena truncatula from the Madagascar rain forest. Journal of natural products. 2006 Feb; 69(2):284-6. doi: 10.1021/np050351x. [PMID: 16499333]
  • You-Xing Zhao, Lu Zhou, Lin Guo, Xiao-Dong Luo, Jun Zhou. A new diterpenoid and active stilbenes from Pinus armandii heartwood. Journal of Asian natural products research. 2005 Jun; 7(3):259-64. doi: 10.1080/10286020410001690163. [PMID: 15621635]
  • William R McNee, Pierluigi Bonello, Andrew J Storer, David L Wood, Thomas R Gordon. Feeding response of Ips paraconfusus to phloem and phloem metabolites of Heterobasidion annosum-inoculated ponderosa pine, Pinus ponderosa. Journal of chemical ecology. 2003 May; 29(5):1183-202. doi: 10.1023/a:1023885724220. [PMID: 12857030]
  • David J Chitwood. Phytochemical based strategies for nematode control. Annual review of phytopathology. 2002; 40(?):221-49. doi: 10.1146/annurev.phyto.40.032602.130045. [PMID: 12147760]