Bioorganic & Medicinal Chemistry Letters · 2021 · 26 citations · 3 references
PharmacyMedicinal ChemistryPharmacologyDrug DiscoveryLead OptimizationPharmacodynamicsAnalgesic PharmacologyHit-to-lead OptimizationLead Compound DesignLead DiscoveryReceptor PharmacologyStructure-activity Relationship AnalysisAnalgesic Drug MechanismsDrug Receptor PharmacologyLead Compound OptimizationLead Compound ScreeningPain PharmacologyPharmacodynamics Of AnalgesicsReceptor-ligand SelectivityStructure - Pharmacokinetic Relationship Analysis
In previous work, we discovered a lead compound and conducted initial SAR studies on a novel series of dioxotriazines to identify the compound as one of the P2X3 receptor antagonists. This compound showed high P2X3 receptor selectivity and a strong analgesic effect. Although not selected for clinical development, the compound was evaluated from various aspects as a tool compound. In the course of the following study, the molecular structures of the dioxotriazines were modified based on pharmacokinetic/pharmacodynamic (PK/PD) analyses. As a result of these SAR studies, Sivopixant (S-600918) was identified as a clinical candidate with potent and selective antagonistic activity (P2X3 IC50, 4.2 nM; P2X2/3 IC50, 1100 nM) and a strong analgesic effect in the rat partial sciatic nerve ligation model (Seltzer model) of allodynia (ED50, 0.4 mg/kg).
3
Quantitative assessment of tactile allodynia in the rat paw
Sandra R. Chaplan, Flemming W. Bach, J W Pogrel et al. · Journal of Neuroscience Methods · 1994 · 7.9K citations