Junko Tamiya

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.

Effects of dexmedetomidine on cardiorespiratory regulation in spontaneously breathing newborn rats

Junko Tamiya, C. Saiki, Ryoji Ide, 2014, Paediatric anaesthesia.

Sa1221 Rpc1063, a Potent, Selective S1P1 Receptor Modulator, Is Active in a Therapeutic IBD Model and Exhibits Favorable PK/PD Properties in Healthy Volunteers

R. Peach, H. Rosen, M. Boehm, 2013 .

RPC1063, a Potent, Selective S1P1 Receptor Modulator, is Active in Therapeutic Inflammatory Bowel Disease Models and Exhibits Favorable PK/PD Properties in Healthy Volunteers

R. Peach, H. Rosen, M. Boehm, 2009 .

Imidazoline 1 receptor activation preserves respiratory drive in spontaneously breathing newborn rats during dexmedetomidine administration

Junko Tamiya, K. Sunada, C. Saiki, 2017, Paediatric anaesthesia.

A spontaneous bicyclization facilitates a synthesis of (−)-hispidospermidin

E. J. Sorensen, Junko Tamiya, 2003 .

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.

Substituted chromones and quinolones as potent melanin-concentrating hormone receptor 1 antagonists.

B. Dyck, Junko Tamiya, C. Heise, 2006, 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.

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.