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Future Medicinal Chemistry|June 20, 2012
Interview with Graham Warrellow by Isaac BruceGraham WarrellowBioorganic & Medicinal Chemistry Letters|May 2, 2006
Racemic and chiral sulfoxides as potential prodrugs of 4-pyrone COX-2 inhibitorsFrancisco Caturla, Mercè Amat, Raquel F Reinoso, et al.Bioorganic & Medicinal Chemistry Letters|April 18, 2006
Racemic and chiral sulfoxides as potential prodrugs of the COX-2 inhibitors Vioxx and ArcoxiaFrancisco Caturla, Mercè Amat, Raquel F Reinoso, et al.Bioorganic & Medicinal Chemistry Letters|February 3, 2005
Synthesis and structure-activity relationships of piperidinylpyrrolopyridine derivatives as potent and selective H1 antagonistsSilvia Fonquerna, Montse Miralpeix, Lluís Pagès, et al.Journal of Medicinal Chemistry|November 30, 2004
Synthesis and structure-activity relationships of novel histamine H1 antagonists: indolylpiperidinyl benzoic acid derivativesSilvia Fonquerna, Montse Miralpeix, Lluís Pagès, et al.Journal of Medicinal Chemistry|May 2, 2007
Discovery and characterization of 4'-(2-furyl)-N-pyridin-3-yl-4,5'-bipyrimidin-2'-amine (LAS38096), a potent, selective, and efficacious A2B adenosine receptor antagonistBernat Vidal, Arsenio Nueda, Cristina Esteve, et al.Pageof 1