1782-55-4
1782-55-4
Chemical Structure
5-Hydroxyferulic acid
- CAS No.: 1782-55-4
- Formula:C10H10O5
- Molecular Weight:210.18
IUPAC Name: (E)-3-(3,4-dihydroxy-5-methoxyphenyl)acrylic acid
InChIKey: YFXWTVLDSKSYLW-NSCUHMNNSA-N
SMILES: O=C(O)/C=C/C1=CC(OC)=C(O)C(O)=C1
Biological Activity: 5-Hydroxyferulic acid is a hydroxycinnamic acid and is a metabolite of the phenylpropanoid pathway. 5-Hydroxyferulic acid is a precursor in the biosynthesis of sinapic acid and is also a COMT non-esterifed substrate[1][2][3].
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5-Hydroxyferulic acid | 99.43% | 5-Hydroxyferulic acid is a hydroxycinnamic acid and is a metabolite of the phenylpropanoid pathway. 5-Hydroxyferulic acid is a precursor in the biosynthesis of sinapic acid and is also a COMT non-esterifed substrate. | ||||||||||||||||||||
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References
- [1]. K Parvathi, et al. Substrate Preferences of O-methyltransferases in Alfalfa Suggest New Pathways for 3-O-methylation of Monolignols. Plant J. 2001 Jan;25(2):193-202. [Content Brief]
- [2]. S Maury, et al. Tobacco O-methyltransferases Involved in Phenylpropanoid Metabolism. The Different Caffeoyl-Coenzyme A/5-hydroxyferuloyl-coenzyme A 3/5-O-methyltransferase and Caffeic acid/5-hydroxyferulic Acid 3/5-O-methyltransferase Classes Have Distinct Substrate Specificities and Expression Patterns. Plant Physiol. 1999 Sep;121(1):215-24. [Content Brief]
- [3]. Inoue, et al. Substrate Preferences of Caffeic acid/5-hydroxyferulic Acid 3/5-O-methyltransferases in Developing Stems of Alfalfa (Medicago Sativa L.). Arch Biochem Biophys. 2000 Mar 1;375(1):175-82. [Content Brief]
