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Galanthamine N-Oxide_Molecular_structure_CAS_134332-50-6)
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Galanthamine N-Oxide

Catalog No. G188525 Name Toronto Research Chemicals
CAS Number 134332-50-6 Website http://www.trc-canada.com
M. F. C17H21NO4 Telephone +1 (416) 665-9696
M. W. 303.35294 Fax +1 (416) 665-4439
Purity Email info@trc-canada.com
Storage Hygroscopic, -20°C Freezer, Under Inert Atmosphere Chembase ID: 169566

SYNONYMS

IUPAC name
(1S,12S,14R)-14-hydroxy-9-methoxy-4-methyl-11-oxa-4-azatetracyclo[8.6.1.01,12.06,17]heptadeca-6(17),7,9,15-tetraen-4-ium-4-olate
IUPAC Traditional name
(1S,12S,14R)-14-hydroxy-9-methoxy-4-methyl-11-oxa-4-azatetracyclo[8.6.1.01,12.06,17]heptadeca-6(17),7,9,15-tetraen-4-ium-4-olate
Synonyms
Galanthamine 10-Oxide
(4aS,6R,8aS,11R)-4a,5,9,10,11,12-Hexahydro-3-methoxy-11-methyl-6H-benzofuro[3a,3,2-ef][2]benzazepin-6-ol 11-Oxide
Galanthamine β-N-oxide
Nivalin-oxide

DATABASE IDS

CAS Number 134332-50-6

PROPERTIES

Certificate of Analysis Download
Apperance Off-White Solid
Melting Point 136-139°C
Solubility Chloroform
Solubility DMSO
Solubility Methanol.
MSDS Link Download
Storage Condition Hygroscopic, -20°C Freezer, Under Inert Atmosphere

DETAILS

Description (English)
A metabolite of Galanthamine (G188500), a selective acetylcholinesterase inhibitor.

REFERENCES

  • Bickel, U., et al.: Clin. Pharmacol. Ther., 50, 420 (1991)
  • Mannens, G., et al.: Drug Metab. Dispos., 30, 553 (1991)
  • Zhao, Q., et al.: J. Clin. Pharmacol., 42, 428 (1991)
  • Geerts, H., et al.: Brain Res., 1033, 186 (1991)