4-Methylsyringol (BioDeep_00000615806)
Main id: BioDeep_00000017736
PANOMIX_OTCML-2023 natural product
代谢物信息卡片
化学式: C9H12O3 (168.0786402)
中文名称: 4-甲基愈创醇
谱图信息:
最多检出来源 () 0%
Last reviewed on 2024-08-21.
Cite this Page
4-Methylsyringol. BioDeep Database v3. PANOMIX ltd, a top metabolomics service provider from China.
https://query.biodeep.cn/s/4-methylsyringol (retrieved
2024-11-03) (BioDeep RN: BioDeep_00000615806). Licensed
under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).
分子结构信息
SMILES: CC1=CC(=C(C(=C1)OC)O)OC
InChI: InChI=1S/C9H12O3/c1-6-4-7(11-2)9(10)8(5-6)12-3/h4-5,10H,1-3H3
描述信息
4-Methylsyringol is a natural product that can be isolated from hardwood[1].
4-Methylsyringol. CAS Common Chemistry. CAS, a division of the American Chemical Society, n.d. https://commonchemistry.cas.org/detail?cas_rn=6638-05-7 (retrieved 2024-08-21) (CAS RN: 6638-05-7). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).
同义名列表
数据库引用编号
6 个数据库交叉引用编号
- ChEBI: CHEBI:172423
- PubChem: 240925
- Metlin: METLIN86420
- ChEMBL: CHEMBL205268
- CAS: 6638-05-7
- medchemexpress: HY-W100715
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)
1 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
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Plant physiology.
2010 Jun; 153(2):569-79. doi:
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Current opinion in plant biology.
2010 Jun; 13(3):313-20. doi:
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Journal of experimental botany.
2010 Jun; 61(10):2735-44. doi:
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BMC plant biology.
2010 May; 10(?):100. doi:
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The Plant cell.
2010 Apr; 22(4):1033-45. doi:
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Journal of visualized experiments : JoVE.
2010 Mar; ?(37):. doi:
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Molecular bioSystems.
2010 Mar; 6(3):499-515. doi:
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BMC plant biology.
2010 Feb; 10(?):27. doi:
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International journal of molecular sciences.
2010 Feb; 11(2):691-703. doi:
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Organic & biomolecular chemistry.
2010 Feb; 8(3):576-91. doi:
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Planta.
2010 Feb; 231(3):677-91. doi:
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Die Naturwissenschaften.
2010 Feb; 97(2):205-17. doi:
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BMC plant biology.
2010 Jan; 10(?):12. doi:
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BMC bioinformatics.
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BMC plant biology.
2009 Sep; 9(?):124. doi:
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Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology.
2009 Sep; 8(9):1233-43. doi:
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Plant physiology.
2009 Jun; 150(2):621-35. doi:
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The Plant journal : for cell and molecular biology.
2009 May; 58(4):706-14. doi:
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BMC plant biology.
2009 Mar; 9(?):26. doi:
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Journal of agricultural and food chemistry.
2009 Feb; 57(4):1275-81. doi:
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Physiologia plantarum.
2009 Feb; 135(2):196-213. doi:
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The New phytologist.
2009; 184(1):99-113. doi:
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The New phytologist.
2009; 182(1):146-162. doi:
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Methods in molecular biology (Clifton, N.J.).
2009; 581(?):169-83. doi:
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PLoS pathogens.
2009 Jan; 5(1):e1000264. doi:
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Journal of experimental botany.
2009; 60(2):509-21. doi:
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BMC plant biology.
2008 Dec; 8(?):132. doi:
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Planta.
2008 Dec; 229(1):115-27. doi:
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Planta.
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Journal of environmental monitoring : JEM.
2008 Oct; 10(10):1187-94. doi:
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BMC plant biology.
2008 Jun; 8(?):71. doi:
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Journal of industrial microbiology & biotechnology.
2008 May; 35(5):355-366. doi:
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Phytochemistry.
2008 Jan; 69(2):348-55. doi:
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Journal of experimental botany.
2008; 59(13):3691-703. doi:
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The New phytologist.
2008; 179(3):738-750. doi:
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Communicative & integrative biology.
2008; 1(1):20-2. doi:
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