3-(2,4-Dihydroxyphenyl)propanoic acid (BioDeep_00000017539)

   

human metabolite PANOMIX_OTCML-2023 Endogenous


代谢物信息卡片


3-(2,4-Dihydroxyphenyl)propionic acid, >=95.0\\% (HPLC)

化学式: C9H10O4 (182.057906)
中文名称: 3-(2,4-二羟基苯)丙酸, 3-(2,4-二羟基苯)丙酸
谱图信息: 最多检出来源 Homo sapiens(feces) 99.69%

分子结构信息

SMILES: C1=CC(=C(C=C1O)O)CCC(=O)O
InChI: InChI=1S/C9H10O4/c10-7-3-1-6(8(11)5-7)2-4-9(12)13/h1,3,5,10-11H,2,4H2,(H,12,13)

描述信息

3-(2,4-Dihydroxyphenyl)propanoic acid belongs to the class of organic compounds known as phenylpropanoic acids. Phenylpropanoic acids are compounds with a structure containing a benzene ring conjugated to a propanoic acid. 3-(2,4-Dihydroxyphenyl)propanoic acid is an extremely weak basic (essentially neutral) compound (based on its pKa). BioTransformer predicts that 3-(2,4-dihydroxyphenyl)propanoic acid is a product of 3-(2,4-dihydroxyphenyl)prop-2-enoic acid metabolism via a reduction-of-alpha-beta-unsaturated-compounds-pattern1 reaction occurring in human gut microbiota and catalyzed by the abkar1 enzyme (PMID: 30612223).
3-(2,4-Dihydroxyphenyl)propanoic acid (DPPacid) is a potent and competitive tyrosinase inhibitor, inhibits L-Tyrosine and DL-DOPA with an IC50 and a Ki of 3.02 μM and 11.5 μM, respectively[1].
3-(2,4-Dihydroxyphenyl)propanoic acid (DPPacid) is a potent and competitive tyrosinase inhibitor, inhibits L-Tyrosine and DL-DOPA with an IC50 and a Ki of 3.02 μM and 11.5 μM, respectively[1].

同义名列表

26 个代谢物同义名

3-(2,4-Dihydroxyphenyl)propionic acid, >=95.0\\% (HPLC); Propanoic acid, 3-(2,4-dihydroxyphenyl)-; 2,4-Dihydroxy-beta-phenylpropanoic acid; 2,4-Dihydroxy-beta-phenylpropionic acid; 3-(2,4-dihydroxyphenyl) propionic acid; 3-(2,4-dihydroxyphenyl)propionic acid; Benzenepropanoic acid, 2,4-dihydroxy-; 3-(2,4-Dihydroxyphenyl)propanoic acid; 2,4-Dihydroxy-β-phenylpropanoic acid; 3-(24-Dihydroxyphenyl)propionic acid; 3-(2,4-Dihydroxyphenyl)Propionicacid; 2E7EBB5A-9F35-48AE-8361-557F93800936; 2,4-Dihydroxy-β-phenylpropionic acid; 3_24_dihydroxyphenyl_propionic_acid; 2,4-Dihydroxybenzenepropionic acid; 2,4-Dihydroxybenzenepropanoic acid; 3-(2,4-Dihydroxyphenyl)propanoate; 2,4-Dihydroxyphenylpropionic acid; 2,4-Dihydroxyphenylpropanoic acid; 3-(24-Dihydroxyphenyl)propionate; 2,4-Dihydroxyhydrocinnamic acid; HMCMTJPPXSGYJY-UHFFFAOYSA-N; Hydroumbellic acid; NCIOpen2_000618; AI3-13072; DPPA acid



数据库引用编号

10 个数据库交叉引用编号

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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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3 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

  • Xinyang Chen, Aya Haniu, Takehiro Kashiwagi, Hiroyuki Watanabe, Takashi Watanabe, Yoshino Okamoto, Masanobu Suzuki, Chul-Sa Kim. The evaluation of the synergistic effect of 3-(2,4-dihydroxyphenyl)propionic acid and l-ascorbic acid on tyrosinase inhibition. Zeitschrift fur Naturforschung. C, Journal of biosciences. 2017 Mar; 72(3-4):119-121. doi: 10.1515/znc-2016-0095. [PMID: 27442367]
  • Soliman Khatib, Ohad Nerya, Ramadan Musa, Snait Tamir, Tal Peter, Jacob Vaya. Enhanced substituted resorcinol hydrophobicity augments tyrosinase inhibition potency. Journal of medicinal chemistry. 2007 May; 50(11):2676-81. doi: 10.1021/jm061361d. [PMID: 17447749]