Substance
ID:449291
Names and Identifiers
IUPAC name
(2E)-3-(3-hydroxy-4-methoxyphenyl)prop-2-enoic acid
Synonyms
Hesperetinic acidIsoferulic acidHesperetic acid
IUPAC Traditional name
(2E)-3-(3-hydroxy-4-methoxyphenyl)prop-2-enoic acid
Registration numbers
CAS Number
Properties
Product Information
Application(s)
Shown with inhibitive effect of against Staphylococcus aureus
Antihyperglycemic action
Biological Source
Isol. from Cimicifuga racemosa, Catalpa ovata and other plants
Pharmacology Properties
Mechanism of Action
Lowers plasma glucose levels
Molecule Details
No Data Available
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Molecular Spectra
No Data Available
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References
• Bowden, B.F. et al., Aust. J. Chem., 1975, 28, 91, (derivs)
• Kelley, C.J. et al., J.O.C., 1976, 41, 449, (cmr)
• Desai, M.N. et al., CA, 1973, 79, 111369c, (detn, Fe)
• de Silva, S.O. et al., Can. J. Chem., 1979, 57, 1598, (synth, deriv)
• Aldrich Library of 13C and 1H FT NMR Spectra, 1992, 2, 1057C; 1058B, (nmr)
• Blase, F.R. et al., Synth. Commun., 1995, 25, 3187, (synth, Isoferulic acid)
• Achenbach, H. et al., Chem. Ber., 1971, 104, 1468, (isol, deriv)
• Bate-Smith, E.C., Sci. Proc. R. Dublin Soc., 1956, 27, 165, (occur)
• Stuart, J.G. et al., J. Het. Chem., 1987, 24, 1589, (synth, ir, pmr, deriv)
• Aldrich Library of FT-IR Spectra, 1st edn., 1985, 2, 184B; 184D, (ir)
• Dewick, P.M. et al., Chem. Comm., 1968, 673, (biosynth)
• Karrer, W. et al., Konstitution und Vorkommen der Organischen Pflanzenstoffe, 2nd edn., Birkhuser Verlag, Basel, 1972, no. 957
• Garcia-Granda, S. et al., Acta Cryst. C, 1987, 43, 683, (cryst struct)
• Souleman, A.A.M. et al., Nat. Prod. Sci., 1998, 4, 245-252, (Isoferulic acid 3'-sulfate)
• Lewis, R.J., Sax's Dangerous Properties of Industrial Materials, 8th edn., Van Nostrand Reinhold, 1992, CAK375
• Hermann, F.X., Pharmazie, 1956, 11, 433, (rev)
• Swain, T. et al., Phytochemistry, 1970, 9, 2115, (biosynth)