R. Mohammed

Substituted indole-1-acetic acids as potent and selective CRTh2 antagonists-discovery of AZD1981.

S. Teague, S. Thom, A. Cook, 2011, Bioorganic & medicinal chemistry letters.

Potent blockers of the monocarboxylate transporter MCT1: novel immunomodulatory compounds.

A. Davis, D. Ferguson, L. Kingston, 2006, Bioorganic & medicinal chemistry letters.

Optimization of monocarboxylate transporter 1 blockers through analysis and modulation of atropisomer interconversion properties.

T. Potter, R. Lewis, S. St-Gallay, 2007, Journal of medicinal chemistry.

Switching between agonists and antagonists at CRTh2 in a series of highly potent and selective biaryl phenoxyacetic acids.

A. Davis, G. Pairaudeau, S. Thom, 2011, Bioorganic & medicinal chemistry letters.

Cyclization of lithiated pyridine and quinoline carboxamides: synthesis of partially saturated pyrrolopyridines and spirocyclic beta-lactams.

J. Clayden, R. Mohammed, S. D. Hamilton, 2005, Organic letters.

Discovery of small molecule human FPR1 receptor antagonists.

J. Unitt, R. Weaver, A. Baxter, 2009, Bioorganic & medicinal chemistry letters.