4.7 Article

Synthesis, cytotoxicity and liposome preparation of 28-acetylenic betulin derivatives

Journal

BIOORGANIC & MEDICINAL CHEMISTRY
Volume 18, Issue 20, Pages 7252-7259

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.bmc.2010.08.023

Keywords

Betulin; Betulinic acid; SRB assay; 1,3-Dipolar cycloaddition; Liposomes; Antitumor

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Several novel betulin derivatives were prepared and evaluated for their antitumor activity. 3-O-Acetyl-betulinic aldehyde served as an ideal starting material for the synthesis of 28-acetylenic derivatives. These compounds were further transformed into pyrazoles and 1,2,3-triazoles. Also, the synthesis of 3-amino substituted butenolides was carried out. The compounds were screened for their antitumor activity in a panel of 15 human cancer cell lines in a sulforhodamine B (SRB) assay. Several compounds showed a noteworthy antitumor activity. In addition, the possibility of encapsulation into liposomes was examined, thereby resulting in an increased cytotoxicity. The results from a trypan-blue test and from DNA laddering provided evidence for an apoptotic cell death. (C) 2010 Elsevier Ltd. All rights reserved.

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