344299-45-2
Chemical Structure
3,4,5-Trimethoxyphenylacetic acid-d2
- CAS No.: 344299-45-2
- Formula:C11H12D2O5
- Molecular Weight:228.24
IUPAC Name: 1-bromo-4-chlorobenzene-2,3,5,6-d4
InChIKey: DDSJXCGGOXKGSJ-NCYHJHSESA-N
SMILES: COC1=C(C(OC)=CC(C([2H])([2H])C(O)=O)=C1)OC
Biological Activity: 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[1][2].
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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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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 | 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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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.
