Home > Compound List > Product Information
Levodopa_Molecular_structure_CAS_59-92-7)
Click picture or here to close

Levodopa

Catalog No. Bio-0575 Name InterBioScreen
CAS Number 59-92-7 Website http://www.ibscreen.com
M. F. C9H11NO4 Telephone +7 49652 40091
M. W. 197.18794 Fax
Purity Email screen@ibscreen.chg.ru
Storage Chembase ID: 1104

SYNONYMS

IUPAC name
(2S)-2-amino-3-(3,4-dihydroxyphenyl)propanoic acid
IUPAC Traditional name
(2S)-2-amino-3-(3,4-dihydroxyphenyl)propanoic acid
Synonyms
Larodopa
Levopa
Brocadopa
Veldopa
Bendopa
Dopar

DATABASE IDS

CAS Number 59-92-7

PROPERTIES

Application(s) Antiparkinsonian
Biological Source Occurs in seedlings and pods of Vicia faba , in Mucuna pruriens, Sarothamnus scoparius, Stizolobium deeringianum, Stizolobium hassjoo, Aristolochia clematitis and other plants. Also prod. by Bacillus spp.
Mechanism of Action Dopaminergic
Mechanism of Action Able to cross the blood-brain-barrier
Mechanism of Action Decarboxylated into dopamine in the basal ganglia and in the periphery markedly increasing serum dopamine

DETAILS

REFERENCES

  • Aldrich Library of FT-IR Spectra, 1st edn., 1985, 2, 257A; 257B, (ir)
  • Aldrich Library of 13C and 1H FT NMR Spectra, 1992, 2, 1190A; 1190B, (nmr)
  • Chapman, R.F. et al., J.C.S.(C), 1970, 865, (dimer)
  • Vorbruggen, H. et al., Chem. Ber., 1972, 105, 1168, (synth)
  • Griffith, T. et al., Phytochemistry, 1973, 12, 1651, (biosynth)
  • Mostad, A. et al., Acta Chem. Scand., Ser. B, 1974, 28, 1161, (cryst struct)
  • Renth, E.-O., Angew. Chem., Int. Ed., 1975, 14, 361, (synth)
  • Fellman, J.H. et al., Biochim. Biophys. Acta, 1975, 381, 9, (isol, deriv)
  • Bartholini, G. et al., Pharmacol. Ther., Part B, 1975, 1, 407, (rev, pharmacol)
  • Gomez, R. et al., Anal. Profiles Drug Subst., 1976, 5, 189, (rev)
  • Dardenne, G. et al., Phytochemistry, 1977, 16, 1822, (deriv)
  • Yamamoto, H. et al., Polymer, 1977, 18, 979; 1978, 19, 1115, (polym)
  • Fuller, W.D. et al., Biopolymers, 1978, 17, 2939, (polym)
  • Danishevsky, S. et al., Tetrahedron, 1981, 37, 4081, (synth)
  • Nutt, J.G. et al., Clin. Neuropharmacol., 1984, 7, 35, (rev, metab)
  • Laycock, M.V. et al., J. Nat. Prod., 1984, 47, 1033, (isol, sulfate)
  • Lee, M. et al., Chem. Pharm. Bull., 1987, 35, 235, (hplc, bibl, anal)
  • Behrman, E.J. et al., Org. Prep. Proced. Int., 1989, 21, 351, (synth, sulfate)
  • Negwer, M., Organic-Chemical Drugs and their Synonyms, 7th edn., Akademie-Verlag, 1994, 1471, (synonyms)
  • Lewis, R.J., Sax's Dangerous Properties of Industrial Materials, 8th edn., Van Nostrand Reinhold, 1992, DNA200