| Bioactivity | 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]. | ||||||||||||
| Invitro | The product of the alfalfa Caffeic acid/5-hydroxyferulic acid 3/5-O-methyltransferase (COMT) catalyzed methylation of 5-Hydroxyferulic acid is sinapic acid. 5-Hydroxyferulic acid O-methyltransferase activities (pkat mg-1 protein) in stem material from COMT downregulates transgenic alfalfa[1]. | ||||||||||||
| Name | 5-Hydroxyferulic acid | ||||||||||||
| CAS | 1782-55-4 | ||||||||||||
| Formula | C10H10O5 | ||||||||||||
| Molar Mass | 210.18 | ||||||||||||
| Transport | Room temperature in continental US; may vary elsewhere. | ||||||||||||
| Storage |
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5-Hydroxyferulic acid
CAS: 1782-55-4 F: C10H10O5 W: 210.18
5-Hydroxyferulic acid is a hydroxycinnamic acid and is a metabolite of the phenylpropanoid pathway. 5-Hydroxyferulic aci
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