P. von Matt

发表

Discovery of 3-(1H-indol-3-yl)-4-[2-(4-methylpiperazin-1-yl)quinazolin-4-yl]pyrrole-2,5-dione (AEB071), a potent and selective inhibitor of protein kinase C isotypes.

G. Rummel, M. Geiser, S. Cowan-Jacob, 2009, Journal of medicinal chemistry.

Indolyl-naphthyl-maleimides as potent and selective inhibitors of protein kinase C-α/β.

E. Vangrevelinghe, J. Wagner, W. Schuler, 2017, Bioorganic & medicinal chemistry letters.

Argyrins, immunosuppressive cyclic peptides from myxobacteria. I. Production, isolation, physico-chemical and biological properties.

H. Reichenbach, C. Heusser, H. Steinmetz, 2002, The Journal of antibiotics.

Argyrins, immunosuppressive cyclic peptides from myxobacteria. II. Structure elucidation and stereochemistry.

H. Steinmetz, L. Oberer, G. Rihs, 2002, The Journal of antibiotics.

STUDIES OF A CHEMICALLY MODIFIED OLIGODEOXYNUCLEOTIDE CONTAINING A 5-ATOM AMIDE BACKBONE WHICH EXHIBITS IMPROVED BINDING TO RNA

F. Natt, K. Altmann, M. Egli, 2001, Nucleosides, Nucleotides & Nucleic Acids.

RNA-Binding affinities and crystal structure of oligonucleotides containing five-atom amide-based backbone structures.

K. Altmann, M. Egli, C. Wilds, 2006, Biochemistry.

Design and synthesis of potent and selective inhibitors of integrin VLA-4.

M. Sabio, M. Weetall, D. Roche, 2001, Bioorganic & medicinal chemistry letters.

Structure-activity relationship and pharmacokinetic studies of sotrastaurin (AEB071), a promising novel medicine for prevention of graft rejection and treatment of psoriasis.

B. Faller, R. Sedrani, C. Beerli, 2011, Journal of medicinal chemistry.

X‐ray Structures and Feasibility Assessment of CLK2 Inhibitors for Phelan–McDermid Syndrome

N. Stiefl, A. Elhajouji, Ivan Galimberti, 2018, ChemMedChem.