Background: Unconventional Knoevenagel-type indoles have been the topic of interest of
many synthetic chemists because of its promising efficacy in different diseases including cancer.
Objective: To explore the structural requirements of Knoevenagel-type cytotoxic indoles for higher
Methods: Multi-QSAR modeling (MLR, ANN, SVM, Bayesian classification, HQSAR and Topomer
CoMFA) was performed on these analogs.
Results: All these modeling techniques were validated individually and interpreted with the
experimental SAR observations. Phenyl or p-methoxyphenyl substitution at 2nd position, electron
withdrawing groups (such as sulphonyl, cyano etc.) at 3rd position and methoxy substation at 5th
position of the indole scaffold may favor cytotoxicity. Eight new indole molecules were predicted from
the developed QSAR models.
Conclusion: These newly designed compounds may bind to the colchicine binding site of the tubulin
protein as suggested by the molecular docking study.