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

52Citations
Citations of this article
31Readers
Mendeley users who have this article in their library.
Get full text

Abstract

Several novel betulin derivatives were prepared and evaluated for their antitumor activity. 3-O-Acetylbetulinic 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. © 2010 Elsevier Ltd. All rights reserved.

Cite

CITATION STYLE

APA

Csuk, R., Barthel, A., Kluge, R., & Ströhl, D. (2010). Synthesis, cytotoxicity and liposome preparation of 28-acetylenic betulin derivatives. Bioorganic and Medicinal Chemistry, 18(20), 7252–7259. https://doi.org/10.1016/j.bmc.2010.08.023

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free