New 5-Substituted SN38 Derivatives: A Stability Study and Interaction with Model Nicked DNA by NMR and Molecular Modeling Methods.

The new 5-substituted SN-38 derivatives, 5( R )-(N-pyrrolidinyl)methyl-7-ethyl-10-hydroxycamptothecin ( 1 ) and its diastereomer 5( S ) ( 2 ), were investigated using a combination of nuclear magnetic resonance (NMR) spectroscopy and molecular modeling methods. The chemical stability, configuration stability, and propensity to aggregate as a function of concentration were determined using 1 H NMR. The calculated self-association constants ( K a ) were found to be 6.4 mM -1 and 2.9 mM -1 for 1 and 2 , respectively. The NMR experiments were performed to elucidate the interaction of each diastereomer with a nicked decamer duplex, referred to as 3 . The calculated binding constants were determined to be 76 mM -1 and 150 mM -1 for the 1 - 3 and 2 - 3 complexes, respectively. NMR studies revealed that the interaction between 1 or 2 and the nicked decamer duplex occurred at the site of the DNA strand break. To complement these findings, molecular modeling methods and calculation protocols were employed to establish the interaction mode and binding constants and to generate molecular models of the DNA/ligand complexes.