syringol (BioDeep_00001871703)
Main id: BioDeep_00000002660
Volatile Flavor Compounds
代谢物信息卡片
Pyrogallol 1,3-dimethyl ether
化学式: C8H10O3 (154.062991)
中文名称: 2,6-二甲氧基苯酚
谱图信息:
最多检出来源 () 0%
分子结构信息
SMILES: COC1=C(C(=CC=C1)OC)O
InChI: InChI=1S/C8H10O3/c1-10-6-4-3-5-7(11-2)8(6)9/h3-5,9H,1-2H3
描述信息
A member of the class of phenols that is phenol substituted by methoxy groups at positions 2 and 6.
同义名列表
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)
5 个相关的物种来源信息
- 1548133 - Bistorta manshuriensis: 10.4314/AJTCAM.V10I1.9
- 59324 - Gymnadenia conopsea: 10.1248/CPB.54.506
- 1747497 - Mucuna birdwoodiana: 10.1248/CPB.35.2675
- 44685 - Panax japonicus:
- 29760 - Vitis vinifera: 10.3389/FMICB.2017.00457
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
- P Snega Priya, Ajay Guru, Ramu Meenatchi, B Haridevamuthu, Manikandan Velayutham, Boopathi Seenivasan, Raman Pachaiappan, Rajakrishnan Rajagopal, Palaniselvam Kuppusamy, Annie Juliet, Jesu Arockiaraj. Syringol, a wildfire residual methoxyphenol causes cytotoxicity and teratogenicity in zebrafish model.
The Science of the total environment.
2023 Mar; 864(?):160968. doi:
10.1016/j.scitotenv.2022.160968. [PMID: 36549541] - M D Milan Gowda, K Jayachandra, Vikram Joshi, Vaddarahally N Manjuprasanna, Gotravalli V Rudresha, Devadasan Velmurugan, Raman Pachaiappan, Noor Mohamed Jameel, Bannikuppe S Vishwanath. Syringol isolated from Eleusine coracana (L.) Gaertn bran suppresses inflammatory response through the down-regulation of cPLA2, COX-2, IκBα, p38 and MPO signaling in sPLA2 induced mice paw oedema.
Inflammopharmacology.
2022 Oct; 30(5):1853-1870. doi:
10.1007/s10787-022-00983-3. [PMID: 35639234] - Xinwen Zhang, Delphis F Levia, Elvis Osamudiamhen Ebikade, Jeffrey Chang, Dionisios G Vlachos, Changqing Wu. The impact of differential lignin S/G ratios on mutagenicity and chicken embryonic toxicity.
Journal of applied toxicology : JAT.
2022 03; 42(3):423-435. doi:
10.1002/jat.4229. [PMID: 34448506] - Hafiz Saqib Ali, Richard H Henchman, Sam P de Visser. Lignin Biodegradation by a Cytochrome P450 Enzyme: A Computational Study into Syringol Activation by GcoA.
Chemistry (Weinheim an der Bergstrasse, Germany).
2020 Oct; 26(57):13093-13102. doi:
10.1002/chem.202002203. [PMID: 32613677] - Sayuki Oka, Ryo Kuniba, Nozomi Tsuboi, Sayaka Tsuchida, Kazunari Ushida, Shusuke Tomoshige, Kouji Kuramochi. Isolation, synthesis, and biological activities of a bibenzyl from Empetrum nigrum var. japonicum.
Bioscience, biotechnology, and biochemistry.
2020 Jan; 84(1):31-36. doi:
10.1080/09168451.2019.1662279. [PMID: 31794330] - Roland Wedekind, Pekka Keski-Rahkonen, Nivonirina Robinot, Vivian Viallon, Pietro Ferrari, Erwan Engel, Marie-Christine Boutron-Ruault, Yahya Mahamat-Saleh, Francesca Romana Mancini, Tilman Kühn, Theron Johnson, Heiner Boeing, Manuela Bergmann, Anna Karakatsani, Antonia Trichopoulou, Heleni Peppa, Claudia Agnoli, Maria Santucci de Magistris, Domenico Palli, Carlotta Sacerdote, Rosario Tumino, Marc J Gunter, Inge Huybrechts, Augustin Scalbert. Syringol metabolites as new biomarkers for smoked meat intake.
The American journal of clinical nutrition.
2019 12; 110(6):1424-1433. doi:
10.1093/ajcn/nqz222. [PMID: 31559413] - Hongyu Rao, Peibo Li, Hao Wu, Chong Liu, Wei Peng, Weiwei Su. Simultaneous Determination of Six Compounds in Destructive Distillation Extracts of Hawthorn Seed by GC-MS and Evaluation of Their Antimicrobial Activity.
Molecules (Basel, Switzerland).
2019 Nov; 24(23):. doi:
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Proceedings of the National Academy of Sciences of the United States of America.
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2011 Jun; 25(6):707-11. doi:
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BMC genomics.
2011 Jan; 12(?):28. doi:
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2011; 53(2):110-4. doi:
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PloS one.
2011; 6(10):e25705. doi:
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PloS one.
2010 Nov; 5(11):e14021. doi:
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Bioorganic & medicinal chemistry.
2010 Sep; 18(18):6708-14. doi:
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2010 Sep; 88(1):133-42. doi:
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2009 Feb; 155(Pt 2):424-433. doi:
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FEMS microbiology ecology.
2008 Oct; 66(1):158-66. doi:
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2008 Jun; 4(6):e1000094. doi:
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2008 Jun; 22(11):1631-9. doi:
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Phytochemistry.
2008 Jan; 69(2):348-55. doi:
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2004 Jun; 117(3):155-64. doi:
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Planta.
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