作者: Denny Wa , Ferguson Lr , Turner Pr
DOI:
关键词: DNA 、 Mechanism of action 、 Footprinting 、 Stereochemistry 、 Cleavage (embryo) 、 DNase-I Footprinting 、 Chemistry 、 Carboxamide 、 DNase footprinting assay 、 Biochemistry 、 In vitro
摘要: The DNA sequence-specific binding ability of polybenzamide minor groove ligands was investigated. These were compared with the known binder Hoechst 33258, using both DNase I footprinting and chlorambucil interference footprinting. monocationic derivative showed some sequence specific to A/T-rich sequences, as shown by footprinting, but results for biscationic inconclusive. A general non-specific inhibition cleavage at high drug concentrations observed, suggesting these compounds had a low affinity 33258. Using complementary technique, displayed clear preference sites containing least three consecutive adenines and, in contrast analogue, lesser mixed A/T sequences.