Abstract
The reaction of betulinic aldehydes with various carbon nucleophiles gave a series of new betulin derivatives, among them epoxides, glycidic derivatives and β-hydroxy carbonyl compounds. Subsequent transformations of the β-hydroxy carbonyls lead to 1,3-diketo- and α,β-unsaturated betulin derivatives. These compounds were assayed for cytotoxicity using 15 human cancer cell lines and a colorimetric SRB-assay. Several compounds revealed significant antitumour activity. © 2009 Elsevier Ltd. All rights reserved.
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Csuk, R., Barthel, A., Kluge, R., Ströhl, D., Kommera, H., & Paschke, R. (2010). Synthesis and biological evaluation of antitumour-active betulin derivatives. Bioorganic and Medicinal Chemistry, 18(3), 1344–1355. https://doi.org/10.1016/j.bmc.2009.12.024
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