Methyl 4-hydroxyphenylacetate (BioDeep_00000264993)

 

Secondary id: BioDeep_00000866783

PANOMIX_OTCML-2023


Metabolite Card


p-Hydroxyphenyl acetic acid methyl ester

  Formula: C9H10O3 (166.063)
Chinese Names: 对羟基苯乙酸甲酯, 4-羟基苯乙酸甲酯
  Spectrum Hits: Top Source Chinese Herbal Medicine(otcml) 55.56%

Molecular Structure

SMILES: c1(ccc(cc1)O)CC(=O)OC
InChI: InChI=1S/C9H10O3/c1-12-9(11)6-7-2-4-8(10)5-3-7/h2-5,10H,6H2,1H3


Description

Methyl 4-hydroxyphenylacetate, a natural compound, is a methyl ester resulting from the formal condensation of the carboxy group of 4-Hydroxyphenylacetic acid with methanol[1].
Methyl 4-hydroxyphenylacetate, a natural compound, is a methyl ester resulting from the formal condensation of the carboxy group of 4-Hydroxyphenylacetic acid with methanol[1].

Synonyms

30 synonym names

Methyl 4-hydroxyphenylacetate; p-Hydroxyphenyl acetic acid methyl ester; Methyl 4-hydroxyphenylacetate; (4-Hydroxy-phenyl)-acetic acid methyl ester; (4-hydroxyphenyl)acetic acid methyl ester; 2-(4-hydroxyphenyl)acetic acid methyl ester; 4-hydroxy phenyl acetic acid methyl ester; 4-hydroxybenzeneacetic acid methyl ester; 4-Hydroxyphenylacetic acid methl ester; 4-Hydroxyphenylacetic acid methyl ester; 4-hydroxyphenylacetic acid, methyl ester; Acetic acid, (p-hydroxyphenyl)-, methyl ester; AI3-36062; Benzeneacetic acid, 4-hydroxy-, methyl ester; Methy 4-Hydroxyphenylacetate; Methyl (4-hydroxyphenyl)acetate; methyl (4-hydroxyphenyl)ethanoate; Methyl (p-hydroxyphenyl)acetate; methyl 2-(4-hydroxyphenyl)acetate; methyl 4-hydroxybenzeneacetate; Methyl 4-hydroxyphenylacetate, ReagentPlus(R), 99%; Methyl 4-hydroxyphenylacetate, Vetec(TM) reagent grade, 98%; methyl 4-hydroxyphenylethanoate; methyl p-hydroxyphenylacetate; Methyl-2-(4-hydroxyphenyl)acetate; Methyl-4-hydroxyphenylacetate; methyl(4-hydroxyphenyl)acetate; methyl2-(4-hydroxyphenyl)acetate; p-Hydroxyphenylacetic acid methyl ester; WN72UVQ99P



Cross Reference

11 cross reference id

Classification Terms

Related Pathways

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BioCyc(0)

PlantCyc(0)

Biological Process

0 related biological process reactions.

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Plant Reactome(0)

INOH(0)

PlantCyc(0)

COVID-19 Disease Map(0)

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PharmGKB(0)

0 organism taxonomy source information

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  • 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。
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  • 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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Sub-cellular location Genes


Literature Reference

  • Yi-Yuan Shao, Chin-Chu Chen, Hsin-Yi Wang, Hsi-Lin Chiu, Tzong-Hsiung Hseu, Yueh-Hsiung Kuo. Chemical constituents of Antrodia camphorata submerged whole broth. Natural product research. 2008; 22(13):1151-7. doi: 10.1080/14786410601132410. [PMID: 18855215]
  • Sopheareth Mao, Seung-Je Lee, Hoon Hwangbo, Yong-Woong Kim, Keun-Hyung Park, Gyu-Suk Cha, Ro-Dong Park, Kil-Yong Kim. Isolation and characterization of antifungal substances from Burkholderia sp. culture broth. Current microbiology. 2006 Nov; 53(5):358-64. doi: 10.1007/s00284-005-0333-2. [PMID: 17066340]
  • R M Kater, N Carulli, F L Iber. Differences in the rate of ethanol metabolism in recently drinking alcoholic and nondrinking subjects. The American journal of clinical nutrition. 1969 Dec; 22(12):1608-17. doi: 10.1093/ajcn/22.12.1608. [PMID: 5362487]