Chengmin Zhong

A-803467, a potent and selective Na _v 1.8 sodium channel blocker, attenuates neuropathic and inflammatory pain in the rat

Michael F. Jarvis, Prisca Honoré, Char‐Chang Shieh et al. · Proceedings of the National Academy of Sciences · 2007 · 514 citations · Full text

A-740003 [N-(1-{[(Cyanoimino)(5-quinolinylamino) methyl]amino}-2,2-dimethylpropyl)-2-(3,4-dimethoxyphenyl)acetamide], a Novel and Selective P2X7 Receptor Antagonist, Dose-Dependently Reduces Neuropathic Pain in the Rat

Prisca Honoré, Diana L. Donnelly‐Roberts, Marian T. Namovic et al. · Journal of Pharmacology and Experimental Therapeutics · 2006 · 401 citations

TRPV1 Receptors in the CNS Play a Key Role in Broad-Spectrum Analgesia of TRPV1 Antagonists

Minghua Cui, Prisca Honoré, Chengmin Zhong et al. · Journal of Neuroscience · 2006 · 310 citations · Full text

Pain Medicine, Trpv1 Antagonists, Immunology +17

Selective blockade of TRPA1 channel attenuates pathological pain without altering noxious cold sensation or body temperature regulation

Jun Chen, Shailen K. Joshi, Stanley DiDomenico et al. · Pain · 2011 · 269 citations · Full text

A-425619 [1-Isoquinolin-5-yl-3-(4-trifluoromethyl-benzyl)-urea], a Novel Transient Receptor Potential Type V1 Receptor Antagonist, Relieves Pathophysiological Pain Associated with Inflammation and Tissue Injury in Rats

Prisca Honoré, Carol T. Wismer, Joe Mikusa et al. · Journal of Pharmacology and Experimental Therapeutics · 2005 · 254 citations