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DOI: 10.2174/1568011053174864
OpenAccess: Closed
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Cytotoxic and Antitumor Potentialities of Aporphinoid Alkaloids

Caroline Stévigny,Christian Bailly,Joëlle Quetin-Leclercq

Cytotoxic T cell
Chemistry
Stereochemistry
2005
Aporphinoids form an important group of plant secondary metabolites. Some of these compounds are used for a long time in traditional medicine for the treatment of various diseases, from benign syndromes to more severe illnesses. More than 500 aporphine alkaloids have been isolated from various plant families and many of these compounds display potent cytotoxic activities which may be exploited for the design of anticancer agents. Here we review the origin, biosynthesis, structure and cytotoxic properties of the prominent members of this class of compounds. Simple aporphinoids (boldine, dicentrine) as well as oxo-, pro- and dehydro-aporphines, and dimeric forms such as thalicarpine, are discussed here. Their mechanisms of action are not well known but DNA-manipulating enzymes such as polymerases and topoisomerases are among the most frequently cited targets for these benzylisoquinoline compounds. This review presents an updated view of the cytotoxic properties of the aporphinoids and their potential contribution to the development of anticancer agents.
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    Cytotoxic and Antitumor Potentialities of Aporphinoid Alkaloids” is a paper by Caroline Stévigny Christian Bailly Joëlle Quetin-Leclercq published in 2005. It has an Open Access status of “closed”. You can read and download a PDF Full Text of this paper here.