trans-Cinnamic acid (BioDeep_00000017235)

Main id: BioDeep_00000270977

 

human metabolite PANOMIX_OTCML-2023 Endogenous blood metabolite BioNovoGene_Lab2019


代谢物信息卡片


cinnamic acid, 14C-labeled cpd (E)-isomer

化学式: C9H8O2 (148.0524268)
中文名称: 肉桂酸, 肉桂酸, 反式肉桂酸, 反式肉桂酸, 肉桂酸, 肉桂酸, 肉桂酸, 肉桂酸, 反式肉桂酸, 反式肉桂酸, 反式肉桂酸, 反式肉桂酸, 反式肉桂酸, 反式肉桂酸, 反式肉桂酸, 反式肉桂酸
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: c1(/C=C/C(=O)O)ccccc1
InChI: InChI=1S/C9H8O2/c10-9(11)7-6-8-4-2-1-3-5-8/h1-7H,(H,10,11)/b7-6+

描述信息

trans-Cinnamic acid, also known as (e)-cinnamic acid or phenylacrylic acid, belongs to the class of organic compounds known as cinnamic acids. These are organic aromatic compounds containing a benzene and a carboxylic acid group forming 3-phenylprop-2-enoic acid. trans-Cinnamic acid exists in all living species, ranging from bacteria to humans. trans-Cinnamic acid is a sweet, balsam, and cinnamon tasting compound. Outside of the human body, trans-Cinnamic acid is found, on average, in the highest concentration within a few different foods, such as chinese cinnamons, olives, and lingonberries and in a lower concentration in redcurrants, red raspberries, and corianders. trans-Cinnamic acid has also been detected, but not quantified in several different foods, such as common oregano, pepper (spice), fennels, pomegranates, and european cranberries. This could make trans-cinnamic acid a potential biomarker for the consumption of these foods. Cinnamic acid has been shown to be a microbial metabolite; it can be found in Alcaligenes, Brevibacterium, Cellulomonas, and Pseudomonas (PMID:16349793). trans-Cinnamic acid is a potentially toxic compound.
Cinnamic acid is a white crystalline hydroxycinnamic acid, which is slightly soluble in water. It is obtained from oil of cinnamon, or from balsams such as storax. Cinnamic acid is found in many foods, some of which are green bell pepper, olive, pepper (spice), and pear.
Cinnamic acid has potential use in cancer intervention, with IC50s of 1-4.5 mM in glioblastoma, melanoma, prostate and lung carcinoma cells.
Cinnamic acid has potential use in cancer intervention, with IC50s of 1-4.5 mM in glioblastoma, melanoma, prostate and lung carcinoma cells.
trans-Cinnamic acid is a natural antimicrobial, with minimal inhibitory concentration (MIC) of 250 μg/mL against fish pathogen A. sobria, SY-AS1[1].
trans-Cinnamic acid is a natural antimicrobial, with minimal inhibitory concentration (MIC) of 250 μg/mL against fish pathogen A. sobria, SY-AS1[1].

同义名列表

57 个代谢物同义名

cinnamic acid, 14C-labeled cpd (E)-isomer; cinnamic acid, 3H-labeled cpd (Z)-isomer; cinnamic acid, 3H-labeled cpd (E)-isomer; cinnamic acid, sodium salt(Z)-isomer; cinnamic acid, sodium salt(E)-isomer; cinnamic acid, zinc salt(E)-isomer; cinnamic acid, 2-(13)C-labeled cpd; cinnamic acid, 2-(14)C-labeled cpd; cinnamic acid, 3-(14)C-labeled cpd; cinnamic acid, ion(1-)-(E)-isomer; cinnamic acid, (trans)-(E)-isomer; trans-3-Phenyl-2-propenoic acid; cinnamic acid, nickel (+2) salt; cinnamic acid, 13C-labeled cpd; (2E)-3-phenylprop-2-enoic acid; (2E)-3-Phenyl-2-propenoic acid; cinnamic acid, 14C-labeled cpd; (2E)-2-Phenyl-2-propenoic acid; cinnamic acid, potassium salt; PHENYLETHYLENECARBOXYLIC ACID; (E)-3-Phenyl-2-propenoic acid; 3-Phenyl-(e)-2-propenoic acid; (E)-3-phenylprop-2-enoic acid; trans-3-Phenyl-2-propenoate; trans-3-Phenylacrylic acid; cinnamic acid, sodium salt; (2E)-3-Phenyl-2-propenoate; (2E)-2-Phenyl-2-propenoate; 3-Phenyl-2-propenoic acid; (2E)-3-phenylacrylic acid; (E)-3-phenylprop-2-enoate; (e)-3-Phenyl-2-propenoate; trans-beta-Carboxystyrene; cinnamic acid, (Z)-isomer; PHENYLETHYLENECARBOXYLate; .beta-Phenylacrylic acid; (E)-3-Phenylacrylic acid; beta-Phenylacrylic acid; trans-3-Phenylacrylate; cinnamic acid, ion(1-); trans-Β-carboxystyrene; trans-b-Carboxystyrene; (2E)-3-Phenylacrylate; (E)-3-Phenylacrylate; 3-Phenylacrylic acid; Β-phenylacrylic acid; Benzeneacrylic acid; trans-cinnamic acid; Phenylacrylic acid; (2E)-Cinnamic acid; (E)-Cinnamic acid; trans-Zimtsaeure; trans-Cinnamate; Benzeneacrylate; (E)-cinnamate; Cinnamic Acid; cinnamate



数据库引用编号

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代谢反应

0 个相关的代谢反应过程信息。

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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。

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