G. Brandt

Structure-based design of a novel series of azetidine inhibitors of the hepatitis C virus NS3/4A serine protease.

Catherine Caillet, S. Cappelle, M. Liuzzi, 2014, Bioorganic & medicinal chemistry letters.

The discovery of IDX21437: Design, synthesis and antiviral evaluation of 2'-α-chloro-2'-β-C-methyl branched uridine pronucleotides as potent liver-targeted HCV polymerase inhibitors.

J. Bilello, S. Cappelle, I. Serra, 2017, Bioorganic & medicinal chemistry letters.

The synthesis and SAR of 2-arylsulfanyl-phenyl piperazinyl acetic acids as glyT-1 inhibitors.

C. Christoffersen, S. Wren, A. Mørk, 2004, Bioorganic & medicinal chemistry letters.

Enantioselective high-performance liquid chromatography assay of (+)R- and (-)S-alpha-lipoic acid in human plasma.

S. Grieb, G. Niebch, H. Borbe, 1997, Chirality.

Discovery and structural diversity of the hepatitis C virus NS3/4A serine protease inhibitor series leading to clinical candidate IDX320.

Catherine Caillet, S. Cappelle, M. Liuzzi, 2015, Bioorganic & medicinal chemistry letters.

Synthesis and antiviral evaluation of a novel series of homoserine-based inhibitors of the hepatitis C virus NS3/4A serine protease.

Catherine Caillet, M. Liuzzi, C. Musiu, 2015, Bioorganic & medicinal chemistry letters.

In-vitro studies of antibiotic combinations for multiply-resistant coagulase-negative staphylococci.

J. Gullings-Handley, R. Proctor, R. Hamill, 1987, Journal of Antimicrobial Chemotherapy.

Synthesis and SAR studies of analogues of 4-(3,3-dimethyl-butyrylamino)-3,5-difluoro-N-thiazol-2-yl-benzamide (Lu AA41063) as adenosine A2A receptor ligands with improved aqueous solubility.

M. Langgård, B. Bang-Andersen, M. Kreilgaard, 2015, Bioorganic & medicinal chemistry letters.