A series of 8-arylated purine derivatives bearing either an aniline or an alkyl amide at position 6 were found to inhibit glycogen synthase kinase-3, with good selectivity over ten kinases. Molecular modeling studies indicated that the most active compounds (8a and 8e), adopt a planar conformation, close to the shape of AMPPNP in the crystal structure of GSK-3. These compounds are stabilized by hydrophobic contacts between the 8-aromatic group and the protein adenine pocket and by electrostatic contacts.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1016/j.ejmech.2010.04.026 | DOI Listing |
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!