2-Phenylpropanal (BioDeep_00000033984)
human metabolite Endogenous
代谢物信息卡片
化学式: C9H10O (134.073161)
中文名称: 2-苯基丙醛, 2-苯丙醛
谱图信息:
最多检出来源 () 0%
分子结构信息
SMILES: CC(C=O)C1=CC=CC=C1
InChI: InChI=1S/C9H10O/c1-8(7-10)9-5-3-2-4-6-9/h2-8H,1H3
描述信息
(±)-2-Phenylpropanal is found in mushrooms. (±)-2-Phenylpropanal is a flavour ingredien
Found in various mushrooms
同义名列表
45 个代谢物同义名
alpha -Methyl-alpha -toluic aldehyde; alpha-Methyl-alpha-toluic aldehyde; alpha-Methyl-benzeneacetalaldehyde; a-Methylbenzeneacetaldehyde, 9ci; alpha-Methyl-benzeneacetaldehyde; alpha-Methyl phenylacetaldehyde; alpha-Methylbenzeneacetaldehyde; alpha -Methylphenylacetaldehyde; alpha-Methyl-alpha-tolualdehyde; alpha-Methylphenylacetaldehyde; benzeneacetaldehyde, α-methyl-; alpha -Phenylpropionaldehyde; alpha-Phenyl propionaldehyde; a-Methylbenzeneacetaldehyde; Α-methylbenzeneacetaldehyde; alpha-Phenylpropionaldehyde; a-Methylphenylacetaldehyde; Α-methyl-α-toluic aldehyde; a-Methyl-a-toluic aldehyde; Α-methylphenylacetaldehyde; alpha -Formylethylbenzene; alpha-Formylethylbenzene; 2-Phenyl-propionaldehyde; 2-Phenyl propionaldehyde; alpha-Methyltolualdehyde; 2-Phenylpropionaldehyde; Α-phenylpropionaldehyde; a-Phenylpropionaldehyde; (1-Formylethyl)-benzene; Hydratropaldehyde, 8ci; Aldehyd hydratropovy; Α-formylethylbenzene; Hydrotropic aldehyde; Hydratropic aldehyde; a-Formylethylbenzene; alpha-Phenylpropanal; 2-Phenyl-1-propanal; Hydratropa aldehyde; 2-Fenyl-1-propanal; Hydratropaldehyde; 2-Phenylpropanal; 2-Phenylpropenal; Cumene aldehyde; Hyacinthal; FEMA 2886
数据库引用编号
8 个数据库交叉引用编号
- ChEBI: CHEBI:149463
- PubChem: 7146
- HMDB: HMDB0031626
- ChEMBL: CHEMBL3730701
- foodb: FDB008265
- chemspider: 6879
- CAS: 34713-70-7
- CAS: 93-53-8
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)
4 个相关的物种来源信息
- 3635 - Gossypium hirsutum: 10.1021/JF60200A011
- 9606 - Homo sapiens: -
- 137129 - Swertia japonica: 10.1246/BCSJ.56.3477
- 54477 - Vitex agnus-castus: 10.1002/(SICI)1097-0231(199608)10:11<1345::AID-RCM631>3.0.CO;2-4
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
- Simone K Huber, Georg Höfner, Klaus T Wanner. Application of the concept of oxime library screening by mass spectrometry (MS) binding assays to pyrrolidine-3-carboxylic acid derivatives as potential inhibitors of γ-aminobutyric acid transporter 1 (GAT1).
Bioorganic & medicinal chemistry.
2019 07; 27(13):2753-2763. doi:
10.1016/j.bmc.2019.05.001
. [PMID: 31097402] - Anat Levi-Zada, Maayan David, Daniela Fefer, Valeriya Seplyarsky, Avraham Sadowsky, Svetlana Dobrinin, Tamir Ticuchinski, Dafna Harari, Daniel Blumberg, Ezra Dunkelblum. Circadian release of male-specific components of the greater date moth, Aphomia (Arenipses) sabella, using sequential SPME/GC/MS analysis.
Journal of chemical ecology.
2014 Mar; 40(3):236-43. doi:
10.1007/s10886-014-0391-7
. [PMID: 24567046] - Ming-Fang Wang, Chih-Li Han, Shih-Jiun Yin. Substrate specificity of human and yeast aldehyde dehydrogenases.
Chemico-biological interactions.
2009 Mar; 178(1-3):36-9. doi:
10.1016/j.cbi.2008.10.002
. [PMID: 18983993] - Shane G Roller, Christine M Dieckhaus, Webster L Santos, R Duane Sofia, Timothy L Macdonald. Interaction between human serum albumin and the felbamate metabolites 4-Hydroxy-5-phenyl-[1,3]oxazinan-2-one and 2-phenylpropenal.
Chemical research in toxicology.
2002 Jun; 15(6):815-24. doi:
10.1021/tx025509h
. [PMID: 12067249] - C M Dieckhaus, S G Roller, W L Santos, R D Sofia, T L Macdonald. Role of glutathione S-transferases A1-1, M1-1, and P1-1 in the detoxification of 2-phenylpropenal, a reactive felbamate metabolite.
Chemical research in toxicology.
2001 May; 14(5):511-6. doi:
10.1021/tx000141e
. [PMID: 11368548]