物质信息
ID:449577
名称和标识
别名
LuteololLuteolinDigitoflavoneDaphneflavonolFlavopurpol
IUPAC标准名
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4H-chromen-4-one
IUPAC传统名
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4H-chromen-4-one
数据登录号
CAS号
化合物性质
产品相关信息
应用领域
Antiinflammatory
Antispasmodic
Antitumourigenic activity in mice reported
Antitussive agent
Shows anti-HIV activity
生物来源
Occurs in many plants in Leguminosae, Resedaceae, Euphorbiaceae, Umbelliferae, Scrophulariaceae, Fabaceae, Asteraceae, Cistaceae, Passifloraceae, Yerbenaceae and Hepaticae.
First isol. in 1832 from Reseda luteola
药理学性质
生物活性机理
Lipid peroxidation inhibitor in rat liver microsomes
描述信息
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分子图谱
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参考文献
• Nagarathnam, D. et al., J.O.C., 1991, 56, 4884, (synth)
• El-Ansari, M.A. et al., Phytochemistry, 1991, 30, 1169, (derivs)
• Litkei, G. et al., Annalen, 1995, 1711, (synth)
• Cody, V. et al., Plant Flavonoids in Biology and Medicine II, (eds., Cody, V. et al), A.R. Liss, N.Y., 1988, (biol, prop)
• Perkin, A.G., J.C.S., 1900, 77, 1315, (isol)
• Bandyukova, V.A., Khim. Prir. Soedin., 1969, 5, 595
• Plant Flavonoids in Biology and Medicine, (eds. Cody, V. et al), A. R. Liss, N. Y., 1986, (biol, prop)
• Inouye, H. et al., Chem. Ber., 1969, 102, 3009, (synth)
• Dhar, K.L. et al., Planta Med., 1970, 18, 337, (isol, deriv)
• Thieme, H., Tet. Lett., 1968, 2781, (derivs)
• Ono, K., Eur. J. Biochem., 1990, 190, 469, (anti-HIV activity)
• 1994, 87, 107, (Luteolin, pharmacol)
• Youssef, D. et al., Planta Med., 1995, 61, 570, (pmr, cmr)
• Mansour, R.M.A. et al., Phytochemistry, 1983, 22, 2630, (derivs)
• Markham, K.R. et al., J. Nat. Prod., 1987, 50, 660, (derivs)
• Kingston, D.G.I., Tetrahedron, 1971, 27, 2691, (ms)
• Wagner, H. et al., Tet. Lett., 1976, 1799, (nmr)
• Voirin, B., Phytochemistry, 1983, 22, 2107, (uv)
• Nevskaya, E.M., Zh. Anal. Khim., 1972, 27, 1699, (use)
• Diller, E., Ber., 1901, 34, 1452, (isol)
• Tomas, F. et al., Z. Naturforsch., C, 1985, 40, 583
• Karrer, W. et al., Konstitution und Vorkommen der Organischen Pflanzenstoffe, 2nd edn., Birkhuser Verlag, Basel, 1972, nos. 1470; 1473, (occur)
• Chari, V.M. et al., Phytochemistry, 1977, 16, 1273, (nmr)