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Chrysin

Catalog No. Bio-0597 Name InterBioScreen
CAS Number 480-40-0 Website http://www.ibscreen.com
M. F. C15H10O4 Telephone +7 49652 40091
M. W. 254.2375 Fax
Purity Email screen@ibscreen.chg.ru
Storage Chembase ID: 59746

SYNONYMS

IUPAC name
5,7-dihydroxy-2-phenyl-4H-chromen-4-one
IUPAC Traditional name
5,7-dihydroxy-2-phenyl-4H-chromen-4-one
Synonyms
5,7-Dihydroxyflavone
Chrysinic acid

DATABASE IDS

CAS Number 480-40-0

PROPERTIES

Application(s) Shows antifungal activity
Biological Source Isol. from Ulmus sieboldiana, Flourensia resinosa, Oroxylum indicum (bark), Pinus and Scutellaria spp. and others
Mechanism of Action Lipid peroxidation inhibitor in rat liver microsomes

DETAILS

REFERENCES

  • Aldrich Library of FT-IR Spectra, 1st edn., 1985, 2, 95C, (ir)
  • Aldrich Library of 13C and 1H FT NMR Spectra, 1992, 2, 918C, (nmr)
  • Nadkarni, D.R. et al., J.C.S., 1938, 1320, (synth)
  • Marsh, C.A., Biochem. J., 1955, 59, 58, (isol, deriv)
  • Katyal, M. et al., Proc. - Indian Acad. Sci., Sect. A, 1962, 56, 125; CA, 58, 3884c, (detn, Th)
  • Dev, B. et al., Fresenius' Z. Anal. Chem., 1963, 196, 178, (synth, use, deriv)
  • Batterham, T.J. et al., Aust. J. Chem., 1964, 17, 428, (pmr)
  • Katyal, M. et al., Talanta, 1968, 15, 95, (detn, U)
  • Bowie, J.H. et al., J.C.S.(B), 1969, 89, (ms)
  • Asakawa, Y., Bull. Chem. Soc. Jpn., 1971, 44, 2761, (isol)
  • Nevskaya, E.M. et al., Zh. Anal. Khim., 1972, 27, 1699, (reactions)
  • Kingston, D.G.I. et al., Tetrahedron, 1973, 29, 4083, (ms)
  • Wagner, H. et al., Tet. Lett., 1976, 1799, (cmr)
  • Gaydon, E.M. et al., Bull. Soc. Chim. Fr., Part II, 1978, 43, (synth, uv, cmr)
  • Davoust, D. et al., Org. Magn. Reson., 1978, 11, 547, (pmr)
  • Jaipetch, T. et al., Phytochemistry, 1983, 22, 625, (isol)
  • Agrawal, P.K. et al., Tet. Lett., 1983, 177, (cmr)
  • Wollenweber, E. et al., Planta Med., 1985, 50, 459, (isol)
  • Saxena, S. et al., Synthesis, 1985, 697, (synth)
  • Le Floc'h, Y. et al., Tet. Lett., 1986, 27, 5503, (synth)
  • The Flavonoids: Advances in Research since 1980, (Ed. Harborne, J.B.), Chapman and Hall, London, 1988
  • Jung, J.H. et al., Phytochemistry, 1990, 29, 1271, (pmr, cmr)
  • Shen, C.-C. et al., Phytochemistry, 1993, 34, 843, (pmr, cmr)
  • Litkei, G. et al., Annalen, 1995, 1711, (synth, pmr)
  • Hounghton, P.J. et al., Pharm. Pharmacol. Lett., 1997, 7, 96-98, (activity)
  • Rashad, M.A. et al., Phytomedicine, 1998, 5, 375-381, (isol, activity)
  • Lee, J.-M. et al., Synthesis, 2001, 2247-2254, (synth, pmr, cmr)