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Cynaroside

Catalog No. Bio-0221 Name InterBioScreen
CAS Number 5373-11-5 Website http://www.ibscreen.com
M. F. C21H20O11 Telephone +7 49652 40091
M. W. 448.3769 Fax
Purity Email screen@ibscreen.chg.ru
Storage Chembase ID: 154727

SYNONYMS

IUPAC name
2-(3,4-dihydroxyphenyl)-5-hydroxy-7-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-4H-chromen-4-one
IUPAC Traditional name
2-(3,4-dihydroxyphenyl)-5-hydroxy-7-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-4H-chromen-4-one
Synonyms
Flavopurposide
Glucoluteolin
Cinaroside
Luteoloside
Luteolin 7-glucoside
Cynaroside
Daphneflavonoloside

DATABASE IDS

CAS Number 5373-11-5

PROPERTIES

Application(s) Antiischaemic agent
Biological Source Widespread in plants. The commonest of all flavone glycosides
Mechanism of Action eNOS promoter
Mechanism of Action eNOS mRNA expression inducer

DETAILS

REFERENCES

  • Perkin, A.G., J.C.S., 1900, 77, 1315, (isol)
  • Diller, E., Ber., 1901, 34, 1452, (isol)
  • Lovecy, A. et al., J.C.S., 1930, 817
  • Hattori, S. et al., J.A.C.S., 1954, 76, 5792, (Glucoluteolin)
  • Thieme, H., Tet. Lett., 1968, 2781, (derivs)
  • Inouye, H. et al., Chem. Ber., 1969, 102, 3009, (synth)
  • Dhar, K.L. et al., Planta Med., 1970, 18, 337, (isol, deriv)
  • Kingston, D.G.I., Tetrahedron, 1971, 27, 2691, (ms)
  • Karrer, W. et al., Konstitution und Vorkommen der Organischen Pflanzenstoffe, 2nd edn., Birkhuser Verlag, Basel, 1972, nos. 1470; 1473, (occur)
  • Nevskaya, E.M., Zh. Anal. Khim., 1972, 27, 1699, (use)
  • Wagner, H. et al., Tet. Lett., 1976, 1799, (nmr)
  • Chari, V.M. et al., Phytochemistry, 1977, 16, 1273, (nmr)
  • Voirin, B., Phytochemistry, 1983, 22, 2107, (uv)
  • Mansour, R.M.A. et al., Phytochemistry, 1983, 22, 2630, (derivs)
  • Tomas, F. et al., Z. Naturforsch., C, 1985, 40, 583
  • Plant Flavonoids in Biology and Medicine, (eds. Cody, V. et al), A. R. Liss, N. Y., 1986, (biol, prop)
  • Medicine II, (eds., Cody, V. et al), A.R. Liss, N.Y., 1988, (biol, prop)