3H-Phenoxazin-3-one (BioDeep_00000384619)

   

natural product


代谢物信息卡片


3H-Phenoxazin-3-one

化学式: C12H7NO2 (197.0477)
中文名称:
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: C1=CC=C2C(=C1)N=C3C=CC(=O)C=C3O2
InChI: InChI=1S/C12H7NO2/c14-8-5-6-10-12(7-8)15-11-4-2-1-3-9(11)13-10/h1-7H

描述信息

同义名列表

1 个代谢物同义名

3H-Phenoxazin-3-one



数据库引用编号

5 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

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)

10 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。

亚细胞结构定位 关联基因列表


文献列表

  • Lidianys María Lewis-Luján, Ema Carina Rosas-Burgos, Josafat Marina Ezquerra-Brauer, María Guadalupe Burboa-Zazueta, Simon Bernard Iloki Assanga, Teresa Del Castillo-Castro, Giselle Penton, Maribel Plascencia-Jatomea. Inhibition of Pathogenic Bacteria and Fungi by Natural Phenoxazinone from Octopus Ommochrome Pigments. Journal of microbiology and biotechnology. 2022 Aug; 32(8):989-1002. doi: 10.4014/jmb.2206.06043. [PMID: 35909165]
  • Jesús G Zorrilla, Carlos Rial, Daniel Cabrera, José M G Molinillo, Rosa M Varela, Francisco A Macías. Pharmacological Activities of Aminophenoxazinones. Molecules (Basel, Switzerland). 2021 Jun; 26(11):. doi: 10.3390/molecules26113453. [PMID: 34200139]
  • Feng-Xian Yang, Guan-Xiong Hou, Jianying Luo, Jing Yang, Yijun Yan, Sheng-Xiong Huang. New phenoxazinone-related alkaloids from strain Streptomyces sp. KIB-H1318. The Journal of antibiotics. 2018 11; 71(12):1040-1043. doi: 10.1038/s41429-018-0099-y. [PMID: 30218038]
  • Sascha Venturelli, Sebastian Petersen, Tobias Langenecker, Detlef Weigel, Ulrich M Lauer, Claude Becker. Allelochemicals of the phenoxazinone class act at physiologically relevant concentrations. Plant signaling & behavior. 2016 05; 11(5):e1176818. doi: 10.1080/15592324.2016.1176818. [PMID: 27088968]
  • Vincent Lam, Martin Henault, Karine Khougaz, Louis-Jacques Fortin, Marc Ouellet, Roman Melnyk, Anthony Partridge. Resorufin butyrate as a soluble and monomeric high-throughput substrate for a triglyceride lipase. Journal of biomolecular screening. 2012 Feb; 17(2):245-51. doi: 10.1177/1087057111422944. [PMID: 21956174]
  • Arnaldo Glogauer, Viviane P Martini, Helisson Faoro, Gustavo H Couto, Marcelo Müller-Santos, Rose A Monteiro, David A Mitchell, Emanuel M de Souza, Fabio O Pedrosa, Nadia Krieger. Identification and characterization of a new true lipase isolated through metagenomic approach. Microbial cell factories. 2011 Jul; 10(?):54. doi: 10.1186/1475-2859-10-54. [PMID: 21762508]
  • Daniel A Dias, Sylvia Urban. HPLC and NMR studies of phenoxazone alkaloids from Pycnoporus cinnabarinus. Natural product communications. 2009 Apr; 4(4):489-98. doi: . [PMID: 19475991]
  • Mona Knop, Svea Pacyna, Nataliya Voloshchuk, Sandra Kant, Carmen Müllenborn, Ulrike Steiner, Martin Kirchmair, Heinrich W Scherer, Margot Schulz. Zea mays: benzoxazolinone detoxification under sulfur deficiency conditions--a complex allelopathic alliance including endophytic Fusarium verticillioides. Journal of chemical ecology. 2007 Feb; 33(2):225-37. doi: 10.1007/s10886-006-9226-5. [PMID: 17200890]
  • M Panteghini, R Bonora, F Pagani. Measurement of pancreatic lipase activity in serum by a kinetic colorimetric assay using a new chromogenic substrate. Annals of clinical biochemistry. 2001 Jul; 38(Pt 4):365-70. doi: 10.1258/0004563011900876. [PMID: 11471878]