THE CHARACTERIZATION AND STRUCTURE-ACTIVITY EVALUATION OF TOXIC NORDITERPENOID ALKALOIDS FROM 2 DELPHINIUM SPECIES

Citation
Gd. Manners et al., THE CHARACTERIZATION AND STRUCTURE-ACTIVITY EVALUATION OF TOXIC NORDITERPENOID ALKALOIDS FROM 2 DELPHINIUM SPECIES, Journal of natural products, 61(9), 1998, pp. 1086-1089
Citations number
20
Categorie Soggetti
Chemistry Medicinal","Plant Sciences","Pharmacology & Pharmacy",Chemistry
Journal title
ISSN journal
01633864
Volume
61
Issue
9
Year of publication
1998
Pages
1086 - 1089
Database
ISI
SICI code
0163-3864(1998)61:9<1086:TCASEO>2.0.ZU;2-5
Abstract
A new N-(methylsuccinimido)anthranoyllycoctonin norditerpenoid alkaloi d, geyerline, has been isolated and characterized from extracts of the poisonous larkspur Delphinium glaucum. A previously described nordite rpenoid alkaloid, grandiflorine, has also been isolated from Delphiniu m geyeri. Both alkaloids are closely related structurally to the poten t neurotoxin methyllycaconitine, established as the primary toxin in m any larkspurs poisonous to cattle. Mouse bioassay tests showed grandif lorine to possess toxicity comparable to methyllycaconitine, while its synthetically derived monoacetate, grandiflorine acetate, and geyerli ne are significantly less toxic.