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Ogindo, C.O., Khraiwesh, M.H., George Jr., M., Brandy, Y., Brandy, N., Gugssa, A., Ashraf, M., Abbas, M., Southerland, W.M., Lee, C.M., Bakare, O. and Fang, Y. (2016) Novel Drug Design for Chagas Disease via Targeting Trypanosoma cruzi Tubulin: Homology Modeling and Binding Pocket Prediction on Trypanosoma cruzi Tubulin Polymerization Inhibition by Naphthoquinone Derivatives. Bioorganic & Medicinal Chemistry, 24, 3849-3855.
https://doi.org/10.1016/j.bmc.2016.06.031

has been cited by the following article:

• TITLE: Molecular Docking Studies on Anticonvulsant Enaminones Inhibiting Voltage-Gated Sodium Channels

  AUTHORS: Yayin Fang, Jamiya Kirkland, Isis J. Amaye, Patrice Jackson-Ayotunde, Matthew George Jr.

  KEYWORDS: Anticonvulsant, Enaminones, Voltage-Gated Sodium Channels, Structure-Based Drug Design, Molecular Docking, 3D QSAR

  JOURNAL NAME: Open Journal of Physical Chemistry, Vol.9 No.4, November 29, 2019

  ABSTRACT: Epilepsy is described as the most common chronic brain disorder. A typical symptom of epilepsy results in uncontrolled convulsions caused by temporary excessive neuronal discharges. Although several new anticon-vulsants have been introduced, some types of seizures have still not been adequately controlled with these new and current therapies. There is an urgent need to develop new anticonvulsant drugs to control the many different types of seizures. Many studies have shown that the epilepsies involve more than one mechanism and therefore may be responsible for the various types of observed seizures. Recently reported studies have shown that a group of newly synthesized 6 Hz active anticonvulsant fluorinated N-benzamide enaminones exhibited selective inhibitions of voltage-gated sodium (Nav) channels. Nav channels are responsible for the initial inward currents during the depolarization phases of the action potential in excitable cells. The activation and opening of Nav channels result in the initial phases of action potentials. We hypothesize that there is an essential pharmacophore model for the interactions between these enaminones and the active sites of Nav channels. The research reported here is focused on molecular docking studies of the interactions that occur between the fluorinated N-benzamide enaminones and the Nav channels. These studies may open an avenue for designing anticonvulsant drugs by inhibiting Nav channels.