4.4 Article

Stereoelectronic properties of spiroquinazolinones in differential PDE7 inhibitory activity

Journal

JOURNAL OF COMPUTATIONAL CHEMISTRY
Volume 29, Issue 12, Pages 1945-1954

Publisher

WILEY
DOI: 10.1002/jcc.20960

Keywords

molecular electrostatic potential; docking; phosphodiesterase; PDE7; protein-ligand interactions

Funding

  1. NCRR NIH HHS [C06 RR014503, C06 RR-14503-01] Funding Source: Medline

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A detailed computational Study on a series of spiroquinazolinones showing phosphodiesterase 7 (PDE7) inhibitory activity was performed to understand the binding mode and the role of stereoelectronic properties in binding. Our docking studies reproduced the essential hydrogen bonding and hydrophobic interactions for inhibitors of this class of enzymes. The N1 proton of the quinazolinone scaffold was involved in H-bonding to an amide side chain of the conserved glutamine residue in the active site. The central bicyclic ring of the molecules showed hydrophobic and pi-stacking interactions with hydrophobic and aromatic amino acid residues, respectively, present in the PDE7 active site. The docked conformations were optimized with density functional theory (DFT) and DFT electronic properties were calculated. Comparison of molecular electrostatic potential (MEP) plots of inhibitors with the active site of PDE7 suggested that the electronic distribution in the molecules is as important as steric factors for binding of the molecules to the receptor. The hydrogen bonding ability and nucleophilic nature of N1 appeared to be important for governing the interaction with PDE7. For less active inhibitors (pIC(50) < 6.5), the MEP maximum at NI of the spiroquinazolinone ring was high or low based on the electronic properties of the substituents. All the more active molecules (pIC(50) > 6.5) had MEP highest at N3, not N1. Efficient binding of these inhibitors may need some rearrangement of side chains of active-site residues, especially Asn365. This computational modeling study should aid in design of new molecules in this class with improved PDE7 inhibition. (C) 2008 Wiley Periodicals, Inc.

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