Martin W Rowbottom

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.

Structure-activity relationships of 1,3,5-triazine-2,4,6-triones as human gonadotropin-releasing hormone receptor antagonists.

Zhiqian Guo, Chen Chen, S. K. Sullivan, 2005, Bioorganic & medicinal chemistry letters.

Abstract 903: AC708 is a potent and selective inhibitor of CSF1R and reduces tumor associated macrophage infiltration in a breast tumor model .

R. Armstrong, B. Belli, Gang Liu, 2013 .

Potent and orally bioavailable zwitterion GnRH antagonists with low CYP3A4 inhibitory activity.

Zhiqian Guo, Chen Chen, Martin W Rowbottom, 2008, Bioorganic & medicinal chemistry letters.