Maosheng Zhang

发表

Antihyperalgesic Effects of (R,E)-N-(2-Hydroxy-2,3-dihydro-1H-inden-4-yl)-3-(2-(piperidin-1-yl)-4-(trifluoromethyl)phenyl)-acrylamide (AMG8562), a Novel Transient Receptor Potential Vanilloid Type 1 Modulator That Does Not Cause Hyperthermia in Rats

J. Louis, B. H. Manning, N. Gavva, 2008, Journal of Pharmacology and Experimental Therapeutics.

Optimization of a Novel Quinazolinone-Based Series of Transient Receptor Potential A1 (TRPA1) Antagonists Demonstrating Potent in Vivo Activity.

Stephanie D. Geuns-Meyer, N. Gavva, Y. Teffera, 2016, Journal of medicinal chemistry.

AMG2850, a potent and selective TRPM8 antagonist, is not effective in rat models of inflammatory mechanical hypersensitivity and neuropathic tactile allodynia

C. Stucky, N. Gavva, Andy D. Weyer, 2015, Naunyn-Schmiedeberg's Archives of Pharmacology.

Optimization of potency and pharmacokinetic properties of tetrahydroisoquinoline transient receptor potential melastatin 8 (TRPM8) antagonists.

H. Monenschein, M. Bartberger, Yunxin Y Bo, 2014, Journal of medicinal chemistry.

Crystal structures of human glycine receptor α3 bound to a novel class of analgesic potentiators

J. Luther, H. Bregman, Xin Huang, 2016, Nature Structural &Molecular Biology.

AMG2850, a potent and selective TRPM8 antagonist, is not effective in rat models of inflammatory mechanical hypersensitivity and neuropathic tactile allodynia

C. Stucky, N. Gavva, Andy D. Weyer, 2015, Naunyn-Schmiedeberg's Archives of Pharmacology.

Selective antagonism of TRPA1 produces limited efficacy in models of inflammatory- and neuropathic-induced mechanical hypersensitivity in rats

C. Stucky, B. Moyer, Stephanie D. Geuns-Meyer, 2016, Molecular pain.

Pharmacological Assessment of Sepiapterin Reductase Inhibition on Tactile Response in the Rat

P. Andrews, W. McCarty, Steve Schneider, 2019, The Journal of Pharmacology and Experimental Therapeutics.

Special Section on The Opioid Crisis Pharmacological Assessment of Sepiapterin Reductase Inhibition on Tactile Response in the Rat s

P. Andrews, W. McCarty, Steve Schneider, 2019 .

Discovery of TRPM8 Antagonist ( S)-6-(((3-Fluoro-4-(trifluoromethoxy)phenyl)(3-fluoropyridin-2-yl)methyl)carbamoyl)nicotinic Acid (AMG 333), a Clinical Candidate for the Treatment of Migraine.

H. Monenschein, M. Horner, M. Bartberger, 2018, Journal of medicinal chemistry.

Voltage-gated sodium channel function and expression in injured and uninjured rat dorsal root ganglia neurons

B. Moyer, Yi Luo, S. Lehto, 2016, The International journal of neuroscience.

TRPV1 modulator that does not cause hyperthermia in rats

J. Louis, B. H. Manning, N. Gavva, 2008 .

The Discovery and Hit-to-Lead Optimization of Tricyclic Sulfonamides as Potent and Efficacious Potentiators of Glycine Receptors.

H. Bregman, Xin Huang, Liyue Huang, 2017, Journal of medicinal chemistry.

Rat NaV1.7 loss-of-function genetic model: Deficient nociceptive and neuropathic pain behavior with retained olfactory function and intra-epidermal nerve fibers

S. Waxman, B. Moyer, Dong Liu, 2019, Molecular pain.

Heliocoverpa armigera single nucleocapsid nucleopolyhedrovirus ORF52 is a ChaB homologous gene involved in per os infection

Fangliang Zheng, Hongsheng Liu, Chunyu Zhu, 2014, Genes & Genomics.

Antihyperalgesic Effects of (R,E)-N-(2-Hydroxy-2,3-dihydro-1H-inden-4-yl)-3-(2-(piperidin-1-yl)-4-(trifluoromethyl)phenyl)-acrylamide (AMG8562), a Novel Transient Receptor Potential Vanilloid Type 1 Modulator That Does Not Cause Hyperthermia in Rats

J. Louis, B. H. Manning, N. Gavva, 2008, Journal of Pharmacology and Experimental Therapeutics.