Alkylidene branched lupane derivatives: Synthesis and antitumor activity
Date
Authors
Csuk, René
Stark, Sebastian
Nitsche, Christoph
Barthel, Alexander
Siewert, Bianka
Journal Title
Journal ISSN
Volume Title
Publisher
Access Statement
Abstract
Several novel alkylidene branched lupane derivatives have been prepared. Many of these compounds showed a significant cytotoxicity. The most active compound, 2-methylene-betulonic acid, showed IC50 values between 0.2 and 0.6 μM for 15 different human cancer cell lines. Cytotoxicity can be improved by encapsulation in liposomes. These compounds act by triggering apoptotic cell death as shown by DNA-laddering experiments and acridine orange/ethidium bromide staining.
Description
Citation
Collections
Source
European Journal of Medicinal Chemistry
Type
Book Title
Entity type
Publication