2-Amino-aryl-7-aryl-benzoxazoles as potent, selective and orally available JAK2 inhibitorsGERSPACHER, Marc; FURET, Pascal; CHENE, Patrick et al.Bioorganic & medicinal chemistry letters (Print). 2010, Vol 20, Num 5, pp 1724-1727, issn 0960-894X, 4 p.Article

Discovery and SAR of potent, orally available 2,8-diaryl-quinoxalines as a new class of JAK2 inhibitorsPISSOT-SOLDERMANN, Carole; GERSPACHER, Marc; TAVARES, Gisele A et al.Bioorganic & medicinal chemistry letters (Print). 2010, Vol 20, Num 8, pp 2609-2613, issn 0960-894X, 5 p.Article

Cyclic guanidines as dual 5-HT_5A/5-HT₇ receptor ligands : Structure-activity relationship elucidationPETERS, Jens-Uwe; LÜBBERS, Thomas; ALANINE, Alexander et al.Bioorganic & medicinal chemistry letters (Print). 2008, Vol 18, Num 1, pp 256-261, issn 0960-894X, 6 p.Article

Modulation of inflammation and pathology during dengue virus infection by p38 MAPK inhibitor SB203580YILONG FU; YIP, Andy; PECK GEE SEAH et al.Antiviral research. 2014, Vol 110, pp 151-157, issn 0166-3542, 7 p.Article

Cyclic guanidines as dual 5-HT_5A/5-HT₇ receptor ligands : Optimising brain penetrationPETERS, Jens-Uwe; LÜBBERS, Thomas; ALANINE, Alexander et al.Bioorganic & medicinal chemistry letters (Print). 2008, Vol 18, Num 1, pp 262-266, issn 0960-894X, 5 p.Article

Design of novel aminopyrrolidine factor Xa inhibitors from a screening hitZBINDEN, Katrin Groebke; ANSELM, Lilli; RISCH, Philippe et al.European journal of medicinal chemistry. 2009, Vol 44, Num 7, pp 2787-2795, issn 0223-5234, 9 p.Article

Discovery of the imidazo[1,5-α][1,2,4].triazolo[1,5-d][1,4]benzodiazepine scaffold as a novel, potent and selective GABA_A α5 inverse agonist seriesACHERMANN, Guido; BALLARD, Theresa M; KOBLET, Andreas et al.Bioorganic & medicinal chemistry letters (Print). 2009, Vol 19, Num 19, pp 5746-5752, issn 0960-894X, 7 p.Article