2. Academic Validation
  3. Discovery and Evaluation of E0714 as an Antiepileptic Candidate: A Highly Subtype-Selective Kv7 Agonist within the Kv7 Family Designed Based on a Kv7.2-Specific Pocket

Discovery and Evaluation of E0714 as an Antiepileptic Candidate: A Highly Subtype-Selective Kv7 Agonist within the Kv7 Family Designed Based on a Kv7.2-Specific Pocket

  • J Med Chem. 2026 Mar 12;69(5):5729-5748. doi: 10.1021/acs.jmedchem.5c03052.
Kening Qiao 1 2,  Weidong Zhao 3,  Yawen Cao 3,  Tingting Li 1,  Lingfang Wei 1,  Xingang Liu 1,  Yan Liu 1,  Jincan Li 1,  Chunxiao Chen 1,  Fan Zhang 1,  Yang Zhang 1 4,  Xuedong Li 1 4,  Qingzhong Jia 1 2 3 5 4 6
Affiliations

Affiliations

  • 1 School of Pharmacy, Hebei Medical University, Shijiazhuang 050017, China.
  • 2 The Key Laboratory of Neural and Vascular Biology, Ministry of Education, Hebei Medical University, Shijiazhuang 050017, China.
  • 3 Department of Pharmacology, Hebei Medical University, Shijiazhuang 050017, China.
  • 4 National Key Laboratory of New Pharmaceutical Preparations and Excipients, Hebei Medical University, Shijiazhuang 050017, China.
  • 5 The Key Laboratory of New Drug Pharmacology and Toxicology, Hebei Medical University, Shijiazhuang, Hebei 050017, China.
  • 6 The Key Laboratory of Clinical Neurology, Ministry of Education, Hebei Medical University, Shijiazhuang 050017, China.
PMID: 41711326 DOI: 10.1021/acs.jmedchem.5c03052
Abstract

Subtype selectivity is critical in drug development, since off-target effects can restrict clinical application. Kv7.2 is a key target for treating neuronal hyperexcitability disorders. Nonselective activation of Kv7 channels can cause multisystem effects and increase therapeutic risk. Through a detailed analysis of Kv7 subtypes, we identified Kv7.2-specific residues to design a selective binding pocket. E0714 was then developed based on this pocket by virtual screening and compound modification. Electrophysiology assays demonstrated that E0714 potently activates Kv7.2 without significantly affecting Kv7.1, Kv7.3, Kv7.4, or Kv7.5. E0714 exhibited an excellent antiepileptic effect in classical epilepsy models without causing motor coordination problems. Mechanistic studies revealed that E0714 targets the Kv7.2-specific residues F112, Y118, and N289, which are responsible for the compound's subtype-selective activation. These findings clarify the mechanism of action of E0714 and provide a framework for designing highly selective drugs against Other Kv7 subtypes.

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