110642-42-7
110642-42-7
Chemical Structure
(E)-5-Hydroxyferulic acid
- CAS No.: 110642-42-7
- Formula:C10H10O5
- Molecular Weight:210.19
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: (E)-5-Hydroxyferulic acid is the E-isomer of 5-Hydroxyferulic acid (HY-133068). 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 substrat[1][2][3].
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(E)-5-Hydroxyferulic acid | (E)-5-Hydroxyferulic acid is the E-isomer of 5-Hydroxyferulic acid (HY-133068). 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 substrat. | |||||||||||||||||||||
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References
- [1]. Parvathi K, 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]. Maury S, 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 K, 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]
Keywords
