NMR studies of the MDP conjugates with amino-acridine/acridone derivatives

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Abstract

Summary

1H and 13C NMR studies allowed us to determine the structure of anticancer active MDP analogs modified at the C-terminus with amino-acridine/acridone derivatives. The products contain an isoglutamine residue without contamination by their isomers containing a glutamine residue as could be expected based on the literature data.

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