Cinnamyl anthranilate (BioDeep_00000012794)

 

Secondary id: BioDeep_00001868170

human metabolite Volatile Flavor Compounds


代谢物信息卡片


Benzoic acid, 2-amino-, 3-phenyl-2-propenyl ester

化学式: C16H15NO2 (253.110273)
中文名称: 邻氨基苯甲酸肉桂酯, 肉桂基2-氨基苯甲酸酯
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: C1=CC=C(C=C1)C=CCOC(=O)C2=CC=CC=C2N
InChI: InChI=1S/C16H15NO2/c17-15-11-5-4-10-14(15)16(18)19-12-6-9-13-7-2-1-3-8-13/h1-11H,12,17H2/b9-6+

描述信息

Prohibited from use in food.
Prohibited from use in food

同义名列表

24 个代谢物同义名

Benzoic acid, 2-amino-, 3-phenyl-2-propenyl ester; (2Z)-3-Phenylprop-2-en-1-yl 2-aminobenzoic acid; 2-Propen-1-ol, 3-phenyl-, 1-(2-aminobenzoate); 2-Aminobenzoic acid 3-phenyl-2-propenyl ester; 2-Propen-1-ol,3-phenyl-, 1-(2-aminobenzoate); (2Z)-3-phenylprop-2-en-1-yl 2-aminobenzoate; 2-Propen-1-ol, 3-phenyl-, 2-aminobenzoate; 3-Phenyl-2-propen-1-yl 2-aminobenzoate; 3-Phenyl-2-propen-1-ol 2-aminobenzoate; Cinnamylester kyseliny anthranilove; 3-Phenyl-2-propenyl-2-aminobenzoate; 3-Phenyl-2-propen-1-yl anthranilate; 3-Phenyl-2-propenyl anthranilate; Anthranilic acid, cinnamyl ester; 3-Phenyl-2-propenylanthranilate; Cinnamyl alcohol, anthranilate; Cinnamyl anthranilic acid; Cinnamyl O-aminobenzoate; Cinnamyl 2-aminobenzoate; Cinnamyl anthranylate; Cinnamyl anthranilate; FEMA 2295; Cinnamyl anthranilate; Cinnamyl 2-aminobenzoate



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(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)

1 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

  • NULL. NTP toxicology and carcinogenesis studies of trans-cinnamaldehyde (CAS No. 14371-10-9) in F344/N rats and B6C3F1 mice (feed studies). National Toxicology Program technical report series. 2004 Feb; ?(514):1-281. doi: NULL. [PMID: 15146216]
  • Clifford R Elcombe, Jenny Odum, John R Foster, Susan Stone, Susan Hasmall, Anthony R Soames, Ian Kimber, John Ashby. Prediction of rodent nongenotoxic carcinogenesis: evaluation of biochemical and tissue changes in rodents following exposure to nine nongenotoxic NTP carcinogens. Environmental health perspectives. 2002 Apr; 110(4):363-75. doi: 10.1289/ehp.02110363. [PMID: 11940454]
  • A Viswalingam, J Caldwell. Cinnamyl anthranilate causes coinduction of hepatic microsomal and peroxisomal enzymes in mouse but not rat. Toxicology and applied pharmacology. 1997 Feb; 142(2):338-47. doi: 10.1006/taap.1996.8043. [PMID: 9070357]
  • F Keyhanfar, J Caldwell. Factors affecting the metabolism of cinnamyl anthranilate in the rat and mouse. Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association. 1996 Mar; 34(3):241-9. doi: 10.1016/0278-6915(95)00119-0. [PMID: 8621105]
  • J Caldwell, A Anthony, I A Cotgreave, S A Sangster, J D Sutton, B K Bernard, R A Ford. Influence of dose and sex on the disposition and hepatic effects of cinnamyl anthranilate in the B6C3F1 mouse. Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association. 1985 Jun; 23(6):559-66. doi: 10.1016/0278-6915(85)90179-6. [PMID: 4040102]
  • R L Bronaugh, R F Stewart. Methods for in vitro percutaneous absorption studies III: hydrophobic compounds. Journal of pharmaceutical sciences. 1984 Sep; 73(9):1255-8. doi: 10.1002/jps.2600730916. [PMID: 6491945]