951-82-6
Chemical Structure
3,4,5-Trimethoxyphenylacetic acid
- CAS No.: 951-82-6
- Formula:C11H14O5
- Molecular Weight:226.23
IUPAC Name: 2-(3,4,5-trimethoxyphenyl)acetic acid
InChIKey: DDSJXCGGOXKGSJ-UHFFFAOYSA-N
SMILES: C1=C(CC(O)=O)C=C(C(=C1OC)OC)OC
Biological Activity: 3,4,5-Trimethoxyphenylacetic acid is a trimethoxylated phenylacetic acid derivative and also a major metabolite of 3,4,5-trimethoxyphenylethylamine. 3,4,5-Trimethoxyphenylacetic acid is produced from the oxidation of 3,4,5-trimethoxyphenylacetaldehyde catalyzed by mouse CYP2C29, and it also serves as a starting material for the synthesis of intermediates of methoxylated phenylacetamides. 3,4,5‑Trimethoxyphenylacetic acid exhibits no significant cataleptic activity and does not prolong pentobarbital-induced sleep duration. 3,4,5-Trimethoxyphenylacetic acid is used in metabolism-related studies[1][2].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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3,4,5-Trimethoxyphenylacetic acid | 99.70% | 3,4,5-Trimethoxyphenylacetic acid is a trimethoxylated phenylacetic acid derivative and also a major metabolite of 3,4,5-trimethoxyphenylethylamine. 3,4,5-Trimethoxyphenylacetic acid is produced from the oxidation of 3,4,5-trimethoxyphenylacetaldehyde catalyzed by mouse CYP2C29, and it also serves as a starting material for the synthesis of intermediates of methoxylated phenylacetamides. 3,4,5‑Trimethoxyphenylacetic acid exhibits no significant cataleptic activity and does not prolong pentobarbital-induced sleep duration. 3,4,5-Trimethoxyphenylacetic acid is used in metabolism-related studies. | ||||||||||||||||||||
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3,4,5-Trimethoxyphenylacetic acid (Standard) | ≥98% | 3,4,5-Trimethoxyphenylacetic acid (Standard) is the analytical standard of 3,4,5-Trimethoxyphenylacetic acid (HY-W009713). This product is intended for research and analytical applications. 3,4,5-Trimethoxyphenylacetic acid is a trimethoxylated phenylacetic acid derivative and also a major metabolite of 3,4,5-trimethoxyphenylethylamine. 3,4,5-Trimethoxyphenylacetic acid is produced from the oxidation of 3,4,5-trimethoxyphenylacetaldehyde catalyzed by mouse CYP2C29, and it also serves as a starting material for the synthesis of intermediates of methoxylated phenylacetamides. 3,4,5‑Trimethoxyphenylacetic acid exhibits no significant cataleptic activity and does not prolong pentobarbital-induced sleep duration. 3,4,5-Trimethoxyphenylacetic acid is used in metabolism-related studies. | ||||||||||||||||||||
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3,4,5-Trimethoxyphenylacetic acid-d2 | 3,4,5-Trimethoxyphenylacetic acid-d2 is the deuterated-labeled 3,4,5-Trimethoxyphenylacetic acid (HY-W009713). 3,4,5-Trimethoxyphenylacetic acid is a trimethoxylated phenylacetic acid derivative and also a major metabolite of 3,4,5-trimethoxyphenylethylamine. 3,4,5-Trimethoxyphenylacetic acid is produced from the oxidation of 3,4,5-trimethoxyphenylacetaldehyde catalyzed by mouse CYP2C29, and it also serves as a starting material for the synthesis of intermediates of methoxylated phenylacetamides. 3,4,5‑Trimethoxyphenylacetic acid exhibits no significant cataleptic activity and does not prolong pentobarbital-induced sleep duration. 3,4,5-Trimethoxyphenylacetic acid is used in metabolism-related studies. | |||||||||||||||||||||
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References
- [1]. Watanabe K, et al. 3,4,5-Trimethoxyphenylacetaldehyde, an intermediate metabolite of mescaline, is a substrate for microsomal aldehyde oxygenase in the mouse liver. Biological & pharmaceutical bulletin. 1995 May;18(5):696-9.
- [2]. Kim J, et al. Antioxidant activity of 3,4,5-trihydroxyphenylacetamide derivatives. Archives of pharmacal research. 2014 Mar;37(3):324-31.
