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Coenzyme q10

产品号 Bio-0021 公司名称 InterBioScreen
CAS号 303-98-0 公司网站 http://www.ibscreen.com
分子式 C59H90O4 电 话 +7 49652 40091
分子量 863.3435 传 真 +7 49652 40092
纯 度 电子邮件 screen@ibscreen.chg.ru
保 存 Chembase数据库ID: 120166

产品价格信息

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产品别名

标题
Coenzyme q10
IUPAC标准名
2-[(2E,6E,10E,14Z,18E,22E,26E,30Z,34E)-3,7,11,15,19,23,27,31,35,39-decamethyltetraconta-2,6,10,14,18,22,26,30,34,38-decaen-1-yl]-5,6-dimethoxy-3-methylcyclohexa-2,5-diene-1,4-dione
IUPAC传统名
2-[(2E,6E,10E,14Z,18E,22E,26E,30Z,34E)-3,7,11,15,19,23,27,31,35,39-decamethyltetraconta-2,6,10,14,18,22,26,30,34,38-decaen-1-yl]-5,6-dimethoxy-3-methylcyclohexa-2,5-diene-1,4-dione
别名
Ubidecarenone
Ubiquinone 50
Ubiquinone 10

产品登记号

CAS号 303-98-0

产品性质

应用领域 Cardiovascular agent
应用领域 used to treat congestive heart failure
生物来源 Isol. from beef heart and other mammalian sources in which it is the principal representative of its class
生物活性机理 Electron transport chain regulator

产品详细信息

参考文献

  • Gloor, U. et al., Helv. Chim. Acta, 1958, 41, 2357; 1960, 43, 1745, (synth)
  • Lester, R.L. et al., J.A.C.S., 1958, 80, 4751, (isol)
  • Shunk, C.H. et al., J.A.C.S., 1958, 80, 4753, (Coenzymes Q1, Q2, Q3)
  • Crane, F.L. et al., Biochim. Biophys. Acta, 1959, 32, 73, (isol)
  • Gale, P.H. et al., Biochem. Biophys. Res. Commun., 1963, 12, 414, (Coenzyme Q10 (H-10))
  • Gale, P.H. et al., Biochemistry, 1963, 2, 196, (Coenzyme Q10 (H-10))
  • Morimoto, H. et al., Biochem. Z., 1965, 343, 329, (ir, ms, pmr)
  • Lavate, W.V. et al., J. Biol. Chem., 1965, 240, 524, (Coenzyme Q10 (H-10))
  • Friis, P. et al., J.A.C.S., 1966, 88, 4754, (biosynth)
  • Muraca, R.F. et al., J.A.C.S., 1967, 89, 1505, (ms)
  • Morimoto, H. et al., Annalen, 1969, 729, 158, (ir, pmr, uv, ms)
  • Karrer, W. et al., Konstitution und Vorkommen der Organischen Pflanzenstoffe, 2nd edn., Birkhuser Verlag, Basel, 1972, nos. 4256-4260, (occur, bibl)
  • The Vitamins, (Sebrell, W.H. et al, Ed.), Academic Press, 1972, 355, (rev)
  • Inoue, S. et al., Bull. Chem. Soc. Jpn., 1974, 47, 3098-3101, (synth, ir, pmr, uv)
  • Hegedus, L.S. et al., J.A.C.S., 1976, 98, 3901
  • Biomed. Clin. Aspects Coenzyme Q, Elsevier, N.Y., 1977, 1-3, (books)
  • Terao, S. et al., J.C.S. Perkin 1, 1978, 1101, (cmr, pmr)
  • Terao, S. et al., J.O.C., 1979, 44, 868, (synth)
  • Naruta, Y., J.O.C., 1980, 45, 4097, (synth)
  • Boicelli, C.A. et al., Membr. Biochem., 1981, 4, 105, (pmr, cmr, config)
  • Fujita, Y. et al., Bull. Chem. Soc. Jpn., 1982, 55, 1325, (synth)
  • Cascone, A. et al., Boll. Chim. Farm., 1984, 123, 555, (pharmacol, Ubidecarenone)
  • Masaki, Y. et al., Chem. Pharm. Bull., 1984, 32, 3959, (synth)
  • Kaln, A. et al., Acta Chem. Scand., Ser. B, 1987, 41, 70, (biosynth)
  • Konishi, K. et al., Chem. Pharm. Bull., 1987, 35, 1531, (biochem, bibl)
  • Negwer, M., Organic-Chemical Drugs and their Synonyms, 6th edn., Akademie-Verlag, 1987, 8345, (synonyms)
  • Eren, D. et al., J.A.C.S., 1988, 110, 4356, (synth)
  • Greenberg, S.M. et al., Med. Clin. North Am., 1988, 72, 243, (rev, pharmacol)
  • Morimoto, H. et al., Naturwissenschaften, 1989, 76, 200-205, (synth)
  • Rttimann, A. et al., Helv. Chim. Acta, 1990, 73, 790, (synth, bibl)
  • Martindale, The Extra Pharmacopoeia, 30th edn.,
  • Lipshutz, B.H. et al., J.A.C.S., 1996, 118, 5512, (synth)
  • Giner, J.-L. et al., Tet. Lett., 1998, 39, 8021-8022, (biosynth)
  • Lipshutz, B.H. et al., J.A.C.S., 1999, 121, 11664-11673, (synth)
  • Tran, M.T. et al., Pharmacotherapy (Carlisle, Mass.), 2001, 21, 797-806, (coenzyme Q10, rev)
  • Ferrante, R.J. et al., J. Neurosci., 2002, 22, 1592-1599, (coenzyme Q10, pharmacol)
  • Lewis, R.J., Sax's Dangerous Properties of Industrial Materials, 8th edn., Van Nostrand Reinhold, 1992, UAH000