R. Schindler

发表

Highly potent, selective, and orally active phosphodiesterase 10A inhibitors.

U. Egerland, N. Hoefgen, M. Malamas, 2011, Journal of medicinal chemistry.

5-(4-Hydroxy-6-methyl-2-oxo-2H-pyran-3-yl)-7-phenyl-2,3,6,7-tetrahydro-1,4-thiazepines as compounds with high affinity at the benzodiazepine binding site on GABA(A) receptors.

U. Egerland, R. Schindler, C. Grunwald, 2011, Die Pharmazie.

Structure-activity relationships in a series of colchicine analogs.

R. Schindler, 1965, Journal of Pharmacology and Experimental Therapeutics.

Ribosidation as a means of activating 6-azauracil as an inhibitor of cell reproduction.

R. Schindler, A. D. Welch, 1957, Science.

Discovery of imidazo[1,5-a]pyrido[3,2-e]pyrazines as a new class of phosphodiesterase 10A inhibitiors.

Christian Grunwald, Ute Egerland, U. Egerland, 2010, Journal of medicinal chemistry.

Chemistry of 4-Amino-thiazoline-2-thiones. Part 2

R. Schindler, M. Gruner, K. Gewald, 1995 .

1,5‐Disubstituted Indazol‐3‐ols with Anti‐Inflammatory Activity

U. Egerland, R. Schindler, I. Szelenyi, 1998, Archiv der Pharmazie.

Novel triazines as potent and selective phosphodiesterase 10A inhibitors.

U. Egerland, N. Hoefgen, M. Malamas, 2012, Bioorganic & medicinal chemistry letters.

Novel triazines as potent and selective phosphodiesterase 10A inhibitors.

U. Egerland, N. Hoefgen, M. Malamas, 2012, Bioorganic & medicinal chemistry letters.

New Method of Synthesis of 5,6-Dihydro-4H-pyrrolo[1,2-a][1,4]benzodiazepines.

R. Schindler, G. Mokrov, R. Gewald, 2008 .