Imma Moreno

Structure-activity relationships (SAR) and structure-kinetic relationships (SKR) of bicyclic heteroaromatic acetic acids as potent CRTh2 antagonists III: the role of a hydrogen-bond acceptor in long receptor residence times.

M. Calbet, E. Gómez, R. S. Roberts, 2014, Bioorganic & medicinal chemistry letters.

Structure-activity relationships (SAR) and structure-kinetic relationships (SKR) of bicyclic heteroaromatic acetic acids as potent CRTh2 antagonists II: lead optimization.

M. Calbet, M. Zanuy, P. Eichhorn, 2014, Bioorganic & medicinal chemistry letters.

2-(1H-Pyrazol-1-yl)acetic acids as chemoattractant receptor-homologous molecule expressed on Th2 lymphocytes (CRTh2) antagonists.

M. Lehner, M. Calbet, P. Eichhorn, 2014, European journal of medicinal chemistry.

2-(1H-Pyrazol-4-yl)acetic acids as CRTh2 antagonists.

M. Lehner, M. Calbet, P. Eichhorn, 2013, Bioorganic & medicinal chemistry letters.

Discovery of a novel class of zwitterionic, potent, selective and orally active S1P₁ direct agonists.

G. Tarrasón, V. Segarra, D. Casals, 2012, Bioorganic & medicinal chemistry letters.

Biphenyl Pyridazinone Derivatives as Inhaled PDE4 Inhibitors: Structural Biology and Structure-Activity Relationships.

M. Lehner, V. Segarra, P. Eichhorn, 2016, Journal of medicinal chemistry.

Biaryl analogues of teriflunomide as potent DHODH inhibitors.

P. Pizcueta, N. Godessart, R. F. Reinoso, 2011, Bioorganic & medicinal chemistry letters.

Structure-activity relationships (SAR) and structure-kinetic relationships (SKR) of pyrrolopiperidinone acetic acids as CRTh2 antagonists.

M. Calbet, P. Eichhorn, R. S. Roberts, 2014, Bioorganic & medicinal chemistry letters.