L. J. Russell

Identification of orally bioavailable small-molecule inhibitors of hematopoietic prostaglandin D2 synthase using X-ray fragment based drug discovery

Paul N. Mortenson, Melanie V. Leveridge, S. Teague, 2014 .

Heteroalicyclic carboxamidines as inhibitors of inducible nitric oxide synthase; the identification of (2R)-2-pyrrolidinecarboxamidine as a potent and selective haem-co-ordinating inhibitor.

James M. Woolven, Richard Graham Knowles, S. Hodgson, 2011, Bioorganic & medicinal chemistry letters.

Antagonism of human CC-chemokine receptor 4 can be achieved through three distinct binding sites on the receptor

S. Hodgson, D. Hall, R. Slack, 2013, Pharmacology research & perspectives.

The discovery of phthalazinone-based human H1 and H3 single-ligand antagonists suitable for intranasal administration for the treatment of allergic rhinitis.

Kenneth L. Clark, Duncan S. Holmes, Michael Kranz, 2011, Journal of medicinal chemistry.

Characterization of selective Calcium-Release Activated Calcium channel blockers in mast cells and T-cells from human, rat, mouse and guinea-pig preparations.

R. Solari, L. J. Russell, H. Bax, 2013, European journal of pharmacology.

GW274150 and GW273629 are potent and highly selective inhibitors of inducible nitric oxide synthase in vitro and in vivo

Richard Graham Knowles, S. Moncada, E. Garvey, 2005, British journal of pharmacology.

Characterization of selective Calcium-Release Activated Calcium channel blockers in mast cells and T-cells from human, rat, mouse and guinea-pig preparations.

R. Solari, L. J. Russell, V. Barrett, 2013, European journal of pharmacology.