J. Tickner

Synthesis and pharmacological profile of two novel heterocyclic chromanols, CP-80,798 and CP-85,958, as potent LTD4 receptor antagonists

A. Marfat, L. Melvin, T. Carty, 1995 .

Synthesis and in vitro profile of 7-substituted quinoline chromanols as novel, non-acidic LTB4 antagonists

A. Marfat, L. Melvin, M. Conklyn, 1995 .

Discovery of micromolar PDE IV inhibitors that exhibit much reduced affinity for the [3H]rolipram binding site: 3-norbornyloxy-4-methoxyphenylmethylene oxindoles

A. Marfat, H. Masamune, Jeanene E. Tickner, 1995 .

The synthesis of highly potent, selective, and water-soluble agonists at the human adenosine A3 receptor.

R. J. Hill, D. Knight, J. Oleynek, 2006, Bioorganic & medicinal chemistry letters.

3'-Aminoadenosine-5'-uronamides: discovery of the first highly selective agonist at the human adenosine A3 receptor.

R. J. Hill, D. Knight, J. Oleynek, 2003, Journal of medicinal chemistry.