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Daidzein

产品号 Bio-0281 公司名称 InterBioScreen
CAS号 486-66-8 公司网站 http://www.ibscreen.com
分子式 C15H10O4 电 话 +7 49652 40091
分子量 254.2375 传 真 +7 49652 40092
纯 度 电子邮件 screen@ibscreen.chg.ru
保 存 Chembase数据库ID: 60045

产品价格信息

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产品别名

标题
Daidzein
IUPAC标准名
7-hydroxy-3-(4-hydroxyphenyl)-4H-chromen-4-one
IUPAC传统名
7-hydroxy-3-(4-hydroxyphenyl)-4H-chromen-4-one
别名
Dimethylbiochanin B
Daidzeol
Daizeol

产品登记号

CAS号 486-66-8

产品性质

应用领域 Antioxydant
应用领域 Antiaggregant
应用领域 Antialcoholic
生物来源 Widespread isoflavone in the Leguminosae (Papilionoideae) eg. in Chamaecytisus spp., Cytisus spp., Phaseolus spp. Also from Streptomyces xanthophaeus
生物活性机理 Antioxydant
生物活性机理 Counteract damaging effects of free radicals in tissues, regulates cell division and cell survival

产品详细信息

参考文献

  • Nishiyama, K. et al., Biosci., Biotechnol., Biochem., 1993, 57, 107, (synth)
  • Hirakura, K. et al., Phytochemistry, 1997, 46,
  • Hendrich, S. et al., Handbook of Nutraceuticals and Functional Foods, (ed. Wildman, R.E.C.), CRC Press,, 2001, 55-75, (occur, metab)
  • Ann. Chim. Farm.
  • Farkas, L. et al., Chem. Ber., 1959, 92, 819, (synth)
  • Markham, K.R. et al., Phytochemistry, 1968, 7, 791, (isol)
  • Gupta, S.R. et al., Phytochemistry, 1971, 10, 877, (synth)
  • Dement, W.A., Phytochemistry, 1972, 11, 1089, (isol)
  • Inone, T. et al., Chem. Pharm. Bull., 1974, 22, 1422, (biosynth)
  • Aoyagi, T. et al., J. Antibiot., 1975, 28, 1006; 1979, 32, 217, (rhamnosides)
  • Deshpande, V.H. et al., Indian J. Chem., Sect. B, 1977, 15, 201, (isol)
  • Nakayama, M. et al., Bull. Chem. Soc. Jpn., 1978, 51, 2398, (synth)
  • Jha, H.C. et al., Can. J. Chem., 1980, 58, 1211, (cmr)
  • Ayabe, S. et al., J.C.S. Perkin 1, 1982, 2725, (biosynth, ms)
  • Kobayashi, M. et al., Phytochemistry, 1983, 22, 1257, (isol)
  • Ingham, J.L., Prog. Chem. Org. Nat. Prod., 1983, 43, 1, (rev, occur)
  • Carman, R.M. et al., Aust. J. Chem., 1985, 38, 485, (isol)
  • Breytenbach, J.C., J. Nat. Prod., 1986, 49, 1003, (isol, deriv)
  • Jain, A.C. et al., J.C.S. Perkin 1, 1986, 215, (synth)
  • Murthy, M.S.R. et al., Magn. Reson. Chem., 1986, 24, 225, (cmr)
  • Matsuda, Y. et al., Agric. Biol. Chem., 1988, 52, 3211, (isol, props)