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Luteolin

产品号 Bio-0604 公司名称 InterBioScreen
CAS号 491-70-3 公司网站 http://www.ibscreen.com
分子式 C15H10O6 电 话 +7 49652 40091
分子量 286.2363 传 真 +7 49652 40092
纯 度 电子邮件 screen@ibscreen.chg.ru
保 存 Chembase数据库ID: 70611

产品价格信息

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产品别名

标题
Luteolin
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
别名
Digitoflavone
Flavopurpol
Luteolol
Daphneflavonol

产品登记号

CAS号 491-70-3

产品性质

应用领域 Antiinflammatory
应用领域 Antispasmodic
应用领域 Antitussive agent
应用领域 Antitumourigenic activity in mice reported
应用领域 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
生物活性机理 Lipid peroxidation inhibitor in rat liver microsomes

产品详细信息

参考文献

  • Perkin, A.G., J.C.S., 1900, 77, 1315, (isol)
  • Diller, E., Ber., 1901, 34, 1452, (isol)
  • Thieme, H., Tet. Lett., 1968, 2781, (derivs)
  • Inouye, H. et al., Chem. Ber., 1969, 102, 3009, (synth)
  • Bandyukova, V.A., Khim. Prir. Soedin., 1969, 5, 595
  • 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)
  • Markham, K.R. et al., J. Nat. Prod., 1987, 50, 660, (derivs)
  • Cody, V. et al., Plant Flavonoids in Biology and Medicine II, (eds., Cody, V. et al), A.R. Liss, N.Y., 1988, (biol, prop)
  • Ono, K., Eur. J. Biochem., 1990, 190, 469, (anti-HIV activity)
  • Nagarathnam, D. et al., J.O.C., 1991, 56, 4884, (synth)
  • El-Ansari, M.A. et al., Phytochemistry, 1991, 30, 1169, (derivs)
  • 1994, 87, 107, (Luteolin, pharmacol)
  • Litkei, G. et al., Annalen, 1995, 1711, (synth)
  • Youssef, D. et al., Planta Med., 1995, 61, 570, (pmr, cmr)