Extrapolative prediction using physically-based QSAR.

ABSTRACT: Surflex-QMOD integrates chemical structure and activity data to produce physically-realistic models for binding affinity prediction . Here, we apply QMOD to a 3D-QSAR benchmark dataset and show broad applicability to a diverse set of targets. Testing new ligands within the QMOD model employs automated flexible molecular alignment, with the model itself defining the optimal pose for each ligand. QMOD performance was compared to that of four approaches that depended on manual alignments (CoMFA, two variations of CoMSIA, and CMF). QMOD showed comparable performance to the other methods on a challenging, but structurally limited, test set. The QMOD models were also applied to test a large and structurally diverse dataset of ligands from ChEMBL, nearly all of which were synthesized years after

SUBMITTER: Cleves AE 

PROVIDER: S-EPMC4796382 | biostudies-literature | 2016 Feb

REPOSITORIES: biostudies-literature