Publication details

Nukleofilní adice na protoberberinový a benzofenanthridinový skelet

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Title in English Nucleophilic addition to protoberberine and benzophenanthridine skeleton
Authors

GRYCOVÁ Lenka HULOVÁ Dagmar STANDARA Stanislav MAREK Radek

Year of publication 2006
Type Article in Proceedings
Conference Chemické listy
MU Faculty or unit

Faculty of Science

Citation
Field Organic chemistry
Keywords protoberberine alkaloids;benzophenanthridine alkaloids; nucleophilic addition;N-nucleophiles; biological activity
Description Quaternary protoberberine QPA and benzo[c]phenanthridine QBA alkaloids belong into isoquinoline alkaloids which is part of big group of secondary metabolites. QPA and QBA are characterized by significant biological activity. They can interact with nucleic acids and proteins and display a great variety of pharmacological effects, e.g. antimicrobial, antifungal, anti-inflammatory, antimalarial or cytotoxic. Both of the alkaloids are characteristic by the sensitivity of the polar C=N+ bond to a nucleophilic attack followed by the formation of adducts with substituents at position C-8 or at position C-6.
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