CPD-111 (BioDeep_00000868279)

Main id: BioDeep_00000406090

 

PANOMIX_OTCML-2023


代谢物信息卡片


InChI=1\C7H8O2\c1-5-3-2-4-6(8)7(5)9\h2-4,8-9H,1H

化学式: C7H8O2 (124.05242679999999)
中文名称: 3-甲基邻苯二酚
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: CC1=C(C(=CC=C1)O)O
InChI: InChI=1S/C7H8O2/c1-5-3-2-4-6(8)7(5)9/h2-4,8-9H,1H3

描述信息

3-Methylcatechol is a building block in the chemical synthesis produced by Pseudomonas putida MC2[1].
3-Methylcatechol is a building block in the chemical synthesis produced by Pseudomonas putida MC2[1].

同义名列表

34 个代谢物同义名

InChI=1\C7H8O2\c1-5-3-2-4-6(8)7(5)9\h2-4,8-9H,1H; 4-06-00-05860 (Beilstein Handbook Reference); 1,2-Dihydroxy-3-methylbenzene; 3-Methyl-1,2-dihydroxybenzene; 2,3-Dihydroxytoluene polymer; 1,2-Benzenediol, 3-methyl-; 3-METHYL-BENZENE-1,2-DIOL; 3-Methyl-1,2-benzenediol; 3-methylbenzene-1,2-diol; Pyrocatechol, 3-methyl-; 3-Methylpyrocatechol; 2,3-Dihydroxytoluene; Catechol, 3-methyl-; 3-METHYL CATECHOL; 3-methylcatechol; Dihydroxytoluene; EINECS 207-672-6; 2,3-Toluenediol; M34006_ALDRICH; WLN: QR BQ C1; ZINC00002503; BRN 0774602; AIDS-002962; CHEBI:18404; AIDS002962; ST5409862; NSC 66523; AI3-61047; 488-17-5; NSC66523; CPD-111; C02923; c0125; MBD



数据库引用编号

11 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(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)

3 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

  • Yunbao Liu, Muraleedharan G Nair. An efficient and economical MTT assay for determining the antioxidant activity of plant natural product extracts and pure compounds. Journal of natural products. 2010 Jul; 73(7):1193-5. doi: 10.1021/np1000945. [PMID: 20565070]
  • Bastian Omokoko, Uwe K Jäntges, Martin Zimmermann, Monika Reiss, Winfried Hartmeier. Isolation of the phe-operon from G. stearothermophilus comprising the phenol degradative meta-pathway genes and a novel transcriptional regulator. BMC microbiology. 2008 Nov; 8(?):197. doi: 10.1186/1471-2180-8-197. [PMID: 19014555]
  • Sonja Veljovic-Jovanovic, Biljana Kukavica, Flavia Navari-Izzo. Characterization of polyphenol oxidase changes induced by desiccation of Ramonda serbica leaves. Physiologia plantarum. 2008 Apr; 132(4):407-16. doi: 10.1111/j.1399-3054.2007.01040.x. [PMID: 18248509]
  • Roman Lang, Christoph Mueller, Thomas Hofmann. Development of a stable isotope dilution analysis with liquid chromatography-tandem mass spectrometry detection for the quantitative analysis of di- and trihydroxybenzenes in foods and model systems. Journal of agricultural and food chemistry. 2006 Aug; 54(16):5755-62. doi: 10.1021/jf061118n. [PMID: 16881674]
  • Takashi Hatta, Gouri Mukerjee-Dhar, Jiri Damborsky, Hohzoh Kiyohara, Kazuhide Kimbara. Characterization of a novel thermostable Mn(II)-dependent 2,3-dihydroxybiphenyl 1,2-dioxygenase from a polychlorinated biphenyl- and naphthalene-degrading Bacillus sp. JF8. The Journal of biological chemistry. 2003 Jun; 278(24):21483-92. doi: 10.1074/jbc.m210240200. [PMID: 12672826]