1-Phenyl-1,2-propanedione (BioDeep_00000004336)

 

Secondary id: BioDeep_00000862369, BioDeep_00001868082

human metabolite PANOMIX_OTCML-2023


代谢物信息卡片


3-Phenyl-2,3-propanedione

化学式: C9H8O2 (148.0524268)
中文名称: 1-苯基-1,2-丙二酮
谱图信息: 最多检出来源 Viridiplantae(plant) 3.05%

分子结构信息

SMILES: CC(=O)C(=O)C1=CC=CC=C1
InChI: InChI=1S/C9H8O2/c1-7(10)9(11)8-5-3-2-4-6-8/h2-6H,1H3

描述信息

1-Phenyl-1,2-propanedione is found in coffee and coffee products. 1-Phenyl-1,2-propanedione is present in coffee aroma. 1-Phenyl-1,2-propanedione is a flavouring ingredient.
Present in coffee aroma. Flavouring ingredient. 1-Phenyl-1,2-propanedione is found in coffee and coffee products.
1-Phenylpropane-1,2-dione, isolated from young Ephedra sinica Stapf (Ephedraceae), is biosynthetic precursors of the ephedrine alkaloids[1][2].
1-Phenylpropane-1,2-dione, isolated from young Ephedra sinica Stapf (Ephedraceae), is biosynthetic precursors of the ephedrine alkaloids[1][2].

同义名列表

16 个代谢物同义名

3-Phenyl-2,3-propanedione; 1-Phenyl-1,2-dioxopropane; 1-Phenylpropane-1,2-dione; 1-PHENYL-1,2-PROPANEDIONE; 1-Phenyl-1,2-propandione; Methyl phenyl diketone; Phenyl methyl diketone; Methyl phenyl glyoxal; Benzoyl methyl ketone; Phenylmethyldiketone; Methylphenylglyoxal; Acetyl benzoyl; Acetylbenzoyl; Benzoylacetyl; Pyruvophenone; FEMA 3226



数据库引用编号

14 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(1)

代谢反应

2 个相关的代谢反应过程信息。

Reactome(0)

BioCyc(1)

WikiPathways(0)

Plant Reactome(0)

INOH(0)

PlantCyc(1)

COVID-19 Disease Map(0)

PathBank(0)

PharmGKB(0)

2 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

  • Satoshi Endo, Namiki Miyagi, Toshiyuki Matsunaga, Akira Ikari. Rabbit dehydrogenase/reductase SDR family member 11 (DHRS11): Its identity with acetohexamide reductase with broad substrate specificity and inhibitor sensitivity, different from human DHRS11. Chemico-biological interactions. 2019 May; 305(?):12-20. doi: 10.1016/j.cbi.2019.03.026. [PMID: 30926317]
  • Raz Krizevski, Einat Bar, O R Shalit, Asaf Levy, Jillian M Hagel, Korey Kilpatrick, Frédéric Marsolais, Peter J Facchini, Shimon Ben-Shabat, Yaron Sitrit, Efraim Lewinsohn. Benzaldehyde is a precursor of phenylpropylamino alkaloids as revealed by targeted metabolic profiling and comparative biochemical analyses in Ephedra spp. Phytochemistry. 2012 Sep; 81(?):71-9. doi: 10.1016/j.phytochem.2012.05.018. [PMID: 22727117]
  • Raz Krizevski, Einat Bar, Or Shalit, Yaron Sitrit, Shimon Ben-Shabat, Efraim Lewinsohn. Composition and stereochemistry of ephedrine alkaloids accumulation in Ephedra sinica Stapf. Phytochemistry. 2010 Jun; 71(8-9):895-903. doi: 10.1016/j.phytochem.2010.03.019. [PMID: 20417943]
  • Hiroyuki Arikawa, Hideo Takahashi, Takahito Kanie, Seiji Ban. Effect of various visible light photoinitiators on the polymerization and color of light-activated resins. Dental materials journal. 2009 Jul; 28(4):454-60. doi: 10.4012/dmj.28.454. [PMID: 19721283]
  • Raz Krizevski, Nativ Dudai, Einat Bar, Efraim Lewinsohn. Developmental patterns of phenylpropylamino alkaloids accumulation in khat (Catha edulis, Forsk.). Journal of ethnopharmacology. 2007 Dec; 114(3):432-8. doi: 10.1016/j.jep.2007.08.042. [PMID: 17928181]