Abstract
A series of novel water-soluble β-carbolines bearing a flexible amino side chain was designed, synthesized and evaluated as potent cytotoxic and DNA intercatalating agents. The N9-arylated alkyl substituted β-carbolines represented the most interesting cytotoxic activities. The results suggested that (1) the N9-arylated alkyl substituents of β-carboline nucleus played a very important role in the modulation of the cytotoxic potencies; (2) the length of the alkylamino side chain significantly affected their cytotoxic potency, and N,N-dimethylaminopropylamino substituent were more favorable. In addition, these compounds were found to exhibit significant DNA intercalating potencies. © 2010 Pharmaceutical Society of Japan.
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Chen, Z., Cao, R., Shi, B., Yi, W., Yu, L., Song, H., & Ren, Z. (2010). Synthesis and biological evaluation of novel β-carbolines as potent cytotoxic and DNA intercalating agents. Chemical and Pharmaceutical Bulletin, 58(7), 901–907. https://doi.org/10.1248/cpb.58.901
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