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Coenzyme q10

Catalog No. Bio-0021 Name InterBioScreen
CAS Number 303-98-0 Website http://www.ibscreen.com
M. F. C59H90O4 Telephone +7 49652 40091
M. W. 863.3435 Fax
Purity Email screen@ibscreen.chg.ru
Storage Chembase ID: 120166

SYNONYMS

IUPAC name
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 Traditional name
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
Synonyms
Ubidecarenone
Ubiquinone 50
Ubiquinone 10

DATABASE IDS

CAS Number 303-98-0

PROPERTIES

Application(s) Cardiovascular agent
Application(s) used to treat congestive heart failure
Biological Source Isol. from beef heart and other mammalian sources in which it is the principal representative of its class
Mechanism of Action Electron transport chain regulator

DETAILS

REFERENCES

  • 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