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机译:食欲素受体拮抗剂在临床前疼痛动物模型中的药理学评价
Merck & Co Inc, Merck Res Labs, Dept Neurosci, Kenilworth, NJ USA;
Merck & Co Inc, Merck Res Labs, Dept Med Chem, Kenilworth, NJ USA;
Merck & Co Inc, Merck Res Labs, Dept Vivo Pharmacol, Kenilworth, NJ USA;
Antinociception; formalin pain model; knockout mice; neuropathic pain; orexin; orexin receptor antagonist;
机译:Montelukast, a cysteinyl leukotriene receptor antagonist, exerts local antinociception in animal model of pain through the L-arginine/nitric oxide/ cyclic GMP/KATP channel pathway and PPARc receptors
机译:Synthesis, ligand-receptor modeling studies and pharmacological evaluation of novel 4-modified-2-aryl-1,2,4-triazolo(4,3-a)quinoxalin-1-one derivatives as potent and selective human A3 adenosine receptor antagonists.
机译:Evaluation of SAMP8 Mice as a Model for Sleep-Wake and Rhythm Disturbances Associated with Alzheimer's Disease: Impact of Treatment with the Dual Orexin (Hypocretin) Receptor Antagonist Lemborexant
机译:Experimental Evaluation of Corrosion Modeling on Carbon Steel in Sub-critical and Supercritical CO_2 Environments
机译:Safety Evaluation of Driver Behavior Adaptations in Connected Vehicle Environment Using Microsimulation Modeling =微观仿真建模在互联车辆环境中驾驶员行为适应的安全性评估.
机译:pharmacological evaluation of l IU Wei Z皇姑granules in rats
机译:Effects of a newly developed potent orexin-2 receptor-selective antagonist, compound 1 m, on sleep/wakefulness states in mice