Spectrum5_000309 (BioDeep_00000396531)
Main id: BioDeep_00000007990
PANOMIX_OTCML-2023
代谢物信息卡片
化学式: C15H14O2 (226.0994)
中文名称: 松油基乙烯基单甲醚
谱图信息:
最多检出来源 () 0%
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
Pinosylvin methyl ether is a stilbenoid.
Pinosylvin methyl ether is a natural product found in Alpinia hainanensis, Pinus contorta var. latifolia, and other organisms with data available.
同义名列表
17 个代谢物同义名
Pinosylvin 3-(methyl ether); Pinosylvin, methyl ether; Pinosylvin monomethyl ether, >=97.0\\% (HPLC); Phenol, 3-methoxy-5-[(1E)-2-phenylethenyl]-; 3-methoxy-5-[(E)-2-phenylethenyl]phenol; Phenol, 3-methoxy-5-(2-phenylethenyl)-; (E)-3-Hydroxy-5-methoxystilbene; 3-methoxy-5-[(E)-styryl]phenol; (E)-3-Methoxy-5-styrylphenol; PINOSYLVIN MONO METHYL ETHER; 3-hydroxy-5-methoxystilbene; Pinosylvin monomethyl ether; pinosylvin monomethylether; Pinosylvin methyl ether; 3-Stilbenol, 5-methoxy-; 5-Methoxy-3-stilbenol; Spectrum5_000309; Pinosylvin methyl ether
数据库引用编号
12 个数据库交叉引用编号
- ChEBI: CHEBI:109537
- ChEBI: CHEBI:8227
- PubChem: 5281719
- ChEMBL: CHEMBL186366
- LipidMAPS: LMPK13090013
- ChemIDplus: 0035302706
- CAS: 35302-70-6
- CAS: 5150-38-9
- medchemexpress: HY-N3056
- KEGG: C10276
- PubChem: 12462
- KNApSAcK: 8227
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)
50 个相关的物种来源信息
- 253221 - Alnus sieboldiana:
- 125259 - Alpinia hainanensis: 10.1016/S0031-9422(98)80083-6
- 173906 - Didymochlaena truncatula: 10.1021/NP050351X
- 630296 - Helichrysum chionosphaerum: 10.1016/0031-9422(89)80195-5
- 496644 - Oedera calycina: 10.1016/0031-9422(90)80181-F
- 379275 - Pentzia incana: 10.1016/0031-9422(90)89035-8
- 53134 - Phragmipedium longifolium: 10.1021/NP070014J
- 3318 - Pinaceae: 10.1021/ACS.JNATPROD.7B00384
- 71624 - Pinus attenuata: 10.3891/ACTA.CHEM.SCAND.05-0121
- 71625 - Pinus ayacahuite: 10.3891/ACTA.CHEM.SCAND.05-0121
- 3338 - Pinus balfouriana: 10.3891/ACTA.CHEM.SCAND.05-0121
- 49510 - Pinus canariensis: 10.3891/ACTA.CHEM.SCAND.05-0121
- 70929 - Pinus caribaea: 10.3891/ACTA.CHEM.SCAND.05-0121
- 71627 - Pinus cembroides: 10.3891/ACTA.CHEM.SCAND.05-0121
- 261911 - Pinus clausa: 10.3891/ACTA.CHEM.SCAND.04-1042
- 1281737 - Pinus contorta var. latifolia: 10.3891/ACTA.CHEM.SCAND.03-0759
- 3351 - Pinus coulteri: 10.3891/ACTA.CHEM.SCAND.05-0121
- 190402 - Pinus densata: 10.3891/ACTA.CHEM.SCAND.03-1375
- 71631 - Pinus echinata: 10.3891/ACTA.CHEM.SCAND.05-0121
- 151559 - Pinus flexilis: 10.3891/ACTA.CHEM.SCAND.05-0121
- 368921 - Pinus glabra: 10.3891/ACTA.CHEM.SCAND.05-0121
- 71633 - Pinus halepensis: 10.3891/ACTA.CHEM.SCAND.04-0055
- 55061 - Pinus jeffreyi: 10.3891/ACTA.CHEM.SCAND.03-0770
- 88728 - Pinus koraiensis: 10.3891/ACTA.CHEM.SCAND.05-0121
- 3342 - Pinus krempfii: 10.1016/S0031-9422(00)82789-2
- 71638 - Pinus leiophylla: 10.3891/ACTA.CHEM.SCAND.05-0121
- 71639 - Pinus lumholtzii: 10.3891/ACTA.CHEM.SCAND.05-0121
- 88730 - Pinus massoniana:
- 71642 - Pinus montezumae: 10.3891/ACTA.CHEM.SCAND.05-0121
- 3345 - Pinus monticola: 10.3891/ACTA.CHEM.SCAND.03-1147
- 28528 - Pinus mugo: 10.3891/ACTA.CHEM.SCAND.03-0755
- 164245 - Pinus muricata: 10.3891/ACTA.CHEM.SCAND.05-0121
- 58042 - Pinus nigra: 10.3891/ACTA.CHEM.SCAND.04-0055
- 268872 - Pinus occidentalis: 10.3891/ACTA.CHEM.SCAND.05-0121
- 46836 - Pinus palustris:
- 71647 - Pinus pinaster: 10.3891/ACTA.CHEM.SCAND.04-0055
- 3346 - Pinus pinea: 10.3891/ACTA.CHEM.SCAND.04-0055
- 164241 - Pinus pungens: 10.3891/ACTA.CHEM.SCAND.03-0755
- 3347 - Pinus radiata: 10.3891/ACTA.CHEM.SCAND.03-0763
- 54921 - Pinus resinosa: 10.1139/B69-143
- 164242 - Pinus rigida: 10.3891/ACTA.CHEM.SCAND.05-0121
- 268869 - Pinus sabiniana: 10.3891/ACTA.CHEM.SCAND.05-0121
- 62752 - Pinus sibirica:
- 399189 - Pinus strobiformis: 10.3891/ACTA.CHEM.SCAND.05-0121
- 3348 - Pinus strobus:
- 3349 - Pinus sylvestris: 10.3891/ACTA.CHEM.SCAND.03-0755
- 3352 - Pinus taeda:
- 71654 - Pinus virginiana: 10.3891/ACTA.CHEM.SCAND.03-1381
- 1973297 - Relhania corymbosa: 10.1016/0031-9422(90)80181-F
- 149671 - Swartzia apetala: 10.1590/S0102-695X2009000300005
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] - 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] - 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]