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Acaciin

Catalog No. Bio-0591 Name InterBioScreen
CAS Number 480-36-4 Website http://www.ibscreen.com
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Storage Chembase ID: 179833

SYNONYMS

IUPAC name
5-hydroxy-2-(4-methoxyphenyl)-7-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-({[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}methyl)oxan-2-yl]oxy}-4H-chromen-4-one
IUPAC Traditional name
5-hydroxy-2-(4-methoxyphenyl)-7-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-({[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}methyl)oxan-2-yl]oxy}-4H-chromen-4-one
Synonyms
Linarin
Linaric acid
Buddleoflavonoloside
Acaciin
Acacetin 7-rutinoside

DATABASE IDS

CAS Number 480-36-4

PROPERTIES

Application(s) Antidiabetic
Biological Source Occurs in Linaria vulgaris, Robinia and Micromeria spp. and other plants
Mechanism of Action Aldose reductase inhibitor

DETAILS

REFERENCES

  • Robinson, R. et al., J.C.S., 1926, 128, 2344, (synth)
  • Freudenberg, K. et al., Annalen, 1954, 587, 207, (Acacetin trioside)
  • Shibata, S. et al., Yakugaku Zasshi, 1960, 80, 620; CA, 54, 21488, (pharmacol)
  • Nakaoki, T. et al., CA, 1961, 55, 10803, (deriv)
  • Massicot, J. et al., Bull. Soc. Chim. Fr., 1963, 2712, (pmr)
  • Nogradi, M. et al., Chem. Ber., 1967, 100, 2783, (deriv)
  • Wagner, H. et al., Chem. Ber., 1969, 102, 1445; 2083; 1970, 103, 851, (derivs)
  • Khadzhai, Y. et al., Farmakol. Toksikol. (Moscow), 1969, 32, 451, (pharmacol)
  • Bowie, J.H. et al., J.C.S.(B), 1969, 2, 89, (ms)
  • Okigawa, M. et al., Tet. Lett., 1970, 2935, (deriv)
  • Nevskaya, E.M. et al., Zh. Anal. Khim., 1972, 27, 1699, (use)
  • Wagner, H. et al., Tet. Lett., 1976, 1799, (nmr)
  • Gaydou, E.M. et al., Bull. Soc. Chim. Fr., 1978, 43, (synth, pmr, uv)