Back

AJBLS · Lens · Molecular Docking and ADMET Profiling of Hydantoin Derivatives Targeting Voltage-Gated Sodium Channel (PDB ID: 1N45) for Epilepsy Treatment

PDF

Article · Volume 15, Issue 2 · pp. 353–365

Molecular Docking and ADMET Profiling of Hydantoin Derivatives Targeting Voltage-Gated Sodium Channel (PDB ID: 1N45) for Epilepsy Treatment

Shankesh Sanjay Bhure1, Rohit Jaysing Bhor2, Amol Mohan Shirode3, Harshali Narayan Anap4, Pravin Bapurao Jadhav5, Apurva Ranganath Gosavi5, Anuj Vishnu Algude5

  1. 1Department of Pharmaceutical Chemistry, Pravara Rural College of Pharmacy Pravaranagar, Tal-Rahata, Ahmednagar, Maharashtra, INDIA.
  2. 2Department of Pharmaceutical Chemistry, K. B. H. S. S. Trust Institute of Pharmacy Malegaon, District Nashik, Maharashtra, INDIA.
  3. 3Department of Pharmaceutical Chemistry, Sitabai Thite college of Pharmacy, Shirur, Pune, Maharashtra, INDIA.
  4. 4Department of Pharmaceutical Chemistry, Sandip Institute of Pharmaceutical sciences, Nashik, Maharashtra, INDIA.
  5. 5Department of Pharmaceutical Chemistry, Pravara Rural College of Pharmacy Pravaranagar, Tal-Rahata, Ahmednagar, Maharashtra, INDIA.

Abstract

Introduction: Epilepsy is a chronic neurological disorder characterized by recurrent seizures resulting from abnormal neuronal excitability, often associated with dysfunction of voltage-gated sodium channels. The present study aims to design and evaluate novel hydantoin-based derivatives of Phenytoin (PHT) as potential anticonvulsant agents using comprehensive in silico approaches. Materials and Methods: A series of ten derivatives (SB-1 to SB-10) were designed and assessed for their physicochemical properties, pharmacokinetic behavior, drug-likeness, toxicity profile, and molecular docking interactions with the voltage-gated sodium channel protein (PDB ID: 1N45). Results: Physicochemical analysis demonstrated that most compounds possess favorable drug-like characteristics, including optimal lipophilicity and acceptable topological polar surface area, supporting good membrane permeability. ADME predictions revealed high gastrointestinal absorption and blood-brain barrier permeability for selected derivatives, indicating their potential for central nervous system activity. Discussion: Toxicity assessments suggested low cardiotoxicity and minimal clinical toxicity risk, although moderate mutagenicity was observed in a few compounds, necessitating further validation. Molecular docking studies showed strong binding affinities across all derivatives, with docking scores ranging from -7.5 to -9.5 kcal/mol. Among the series, SB-3 exhibited the highest binding affinity, supported by diverse interactions including electrostatic, hydrophobic, and π-mediated interactions, while SB-8 and SB-9 also demonstrated significant binding stability through multiple hydrogen bonds. Conclusion: The integrated computational findings highlight SB-3 as a promising lead compound, with SB-8 and SB-9 as potential candidates for further development. This study provides valuable insights into the rational design of novel anticonvulsant agents targeting sodium channels and establishes a foundation for future experimental validation and optimization.

Keywords: Anticonvulsant activity; Blood-brain barrier; Drug-likeness; Epilepsy; Hydantoin derivatives; Molecular docking; Voltage-gated sodium channel

The full text of this article is available as a PDF. Open the PDF.