J. Grey

发表

Studies on the structure-activity relationship of bicifadine analogs as monoamine transporter inhibitors.

Beth A. Fleck, Rebecca R. Pick, Mingzhu Zhang, 2008, Bioorganic & medicinal chemistry letters.

Composés capables de moduler le calcium intracellulaire

B. Dyck, J. Grey, Jianguo Cao, 2011 .

Manipulation of small-molecule inhibitory kinetics modulates MCH-R1 function

R. Maki, Mingzhu Zhang, J. Grey, 2006, Molecular and Cellular Endocrinology.

Contrasting effects of different cannabinoid receptor ligands on mouse ingestive behaviour

S. Higgs, J. Grey, P. Terry, 2012, Behavioural pharmacology.

Potent imidazole and triazole CB1 receptor antagonists related to SR141716.

Teresa Y. Phillips, Brock T Brown, B. Dyck, 2004, Bioorganic & medicinal chemistry letters.

Design and Synthesis of Tricyclic Imidazo[4,5- b ]pyridin-2-ones as Corticotropin-Releasing Factor-1 Antagonists

Zhiqian Guo, D. Grigoriadis, B. Dyck, 2005 .

Characterization of thien-2-yl 1S,2R-milnacipran analogues as potent norepinephrine/serotonin transporter inhibitors for the treatment of neuropathic pain.

Beth A. Fleck, Rebecca R. Pick, M. Bradbury, 2008, Journal of medicinal chemistry.

Identification of 1S,2R-milnacipran analogs as potent norepinephrine and serotonin transporter inhibitors.

Beth A. Fleck, Mingzhu Zhang, F. Jovic, 2008, Bioorganic & medicinal chemistry letters.

Bis(aminopyrrolidine)-derived ureas (APUs) as potent MCH1 receptor antagonists.

John Saunders, Liren Zhao, Mingzhu Zhang, 2005, Bioorganic & medicinal chemistry letters.

Synthesis and structure-activity relationships of biarylcarboxamide bis-aminopyrrolidine urea derived small-molecule antagonists of the melanin-concentrating hormone receptor-1 (MCH-R1).

John Saunders, Liren Zhao, D. Provencal, 2005, Bioorganic & medicinal chemistry letters.

Thienopyrimidinone bis-aminopyrrolidine ureas as potent melanin-concentrating hormone receptor-1 (MCH-R1) antagonists.

Mingzhu Zhang, Troy D. Vickers, B. Dyck, 2007, Bioorganic & medicinal chemistry letters.

Studies on a series of milnacipran analogs containing a heteroaromatic group as potent norepinephrine and serotonin transporter inhibitors.

Beth A. Fleck, Mingzhu Zhang, F. Jovic, 2008, Bioorganic & medicinal chemistry letters.

Design and synthesis of tricyclic imidazo[4,5-b]pyridin-2-ones as corticotropin-releasing factor-1 antagonists.

Zhiqian Guo, D. Grigoriadis, B. Dyck, 2005, Journal of Medicinal Chemistry.

Synthesis and structure-activity relationships of retro bis-aminopyrrolidine urea (rAPU) derived small-molecule antagonists of the melanin-concentrating hormone receptor-1 (MCH-R1). Part 1.

Mingzhu Zhang, Troy D. Vickers, B. Dyck, 2006, Bioorganic & medicinal chemistry letters.

Characterization of thien-2-yl 1S,2R-milnacipran analogues as potent norepinephrine/serotonin transporter inhibitors for the treatment of neuropathic pain.

Beth A. Fleck, Rebecca R. Pick, M. Bradbury, 2008, Journal of Medicinal Chemistry.

Studies on the SAR and pharmacophore of milnacipran derivatives as monoamine transporter inhibitors.

M. Mesleh, Beth A. Fleck, Mingzhu Zhang, 2008, Bioorganic & medicinal chemistry letters.