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- URN to cite this document:
- urn:nbn:de:bvb:355-epub-443645
- DOI to cite this document:
- 10.5283/epub.44364
This publication is part of the DEAL contract with Wiley.
Abstract
In previous studies, we demonstrated that esters of bendamustine containing a basic moiety are far more cytotoxic anticancer agents than their parent compound and that the substitution of the labile ester moiety by a branched ester or an amide markedly increases stability in the blood plasma. In the current study, we showed that this substitution was bioisosteric. Aiming at increased ...
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