V. Schattel

发表

Pyridinylquinoxalines and pyridinylpyridopyrazines as lead compounds for novel p38 alpha mitogen-activated protein kinase inhibitors.

S. Laufer, P. Koch, H. Jahns, 2010, Journal of medicinal chemistry.

Tri- and tetrasubstituted imidazoles as p38α mitogen-activated protein kinase inhibitors.

S. Laufer, P. Koch, C. Bracht, 2010, Bioorganic & medicinal chemistry letters.

Design, synthesis and SAR of phenylamino-substituted 5,11-dihydro-dibenzo[a,d]cyclohepten-10-ones and 11H-dibenzo[b,f]oxepin-10-ones as p38 MAP kinase inhibitors.

V. Schattel, A. Dorn, S. Laufer, 2010, Bioorganic & medicinal chemistry letters.

Role of the hydrogen bonding heteroatom-Lys53 interaction between the p38alpha mitogen-activated protein (MAP) kinase and pyridinyl-substituted 5-membered heterocyclic ring inhibitors.

S. Laufer, P. Koch, V. Schattel, 2009, Journal of medicinal chemistry.

3,4-Diaryl-isoxazoles and -imidazoles as potent dual inhibitors of p38alpha mitogen activated protein kinase and casein kinase 1delta.

Mohammed M. Abadleh, U. Knippschild, C. Peifer, 2009, Journal of medicinal chemistry.

Implications for selectivity of 3,4-diarylquinolinones as p38alphaMAP kinase inhibitors.

Mohammed M. Abadleh, O. Kohlbacher, C. Peifer, 2008, Bioorganic & medicinal chemistry letters.

Conformational effects on potency of thioimidazoles and dihydrothiazolines

D. Schollmeyer, W. Albrecht, V. Schattel, 2011 .

Biological Evaluation and Structural Determinants of p38α Mitogen‐Activated‐Protein Kinase and c‐Jun‐N‐Terminal Kinase 3 Inhibition by Flavonoids

S. Laufer, P. Koch, I. Merfort, 2010, Chembiochem : a European journal of chemical biology.

Design, synthesis, and biological evaluation of novel disubstituted dibenzosuberones as highly potent and selective inhibitors of p38 mitogen activated protein kinase.

D. Schollmeyer, Stefan A. Laufer, S. Fischer, 2012, Journal of medicinal chemistry.

A frozen analogue approach to aminopyridinylimidazoles leading to novel and promising p38 MAP kinase inhibitors.

D. Schollmeyer, W. Albrecht, V. Schattel, 2012, Journal of medicinal chemistry.

Targeting the hinge glycine flip and the activation loop: novel approach to potent p38α inhibitors.

S. Laufer, M. Goettert, D. Rauh, 2012, Journal of medicinal chemistry.

Synthesis and Biological Testing of N‐Aminoimidazole‐Based p38α MAP Kinase Inhibitors

Stefan A. Laufer, C. Bracht, W. Albrecht, 2010, ChemMedChem.

Skepinone-L is a selective p38 mitogen-activated protein kinase inhibitor.

Wolfgang Albrecht, Daniel Rauh, Oliver Werz, 2012, Nature chemical biology.

Identification of rosmarinic acid as the major active constituent in Cordia americana.

O. Werz, I. Merfort, B. Heinzmann, 2010, Journal of ethnopharmacology.

Inside Cover: Synthesis and Biological Testing of N-Aminoimidazole-Based p38α MAP Kinase Inhibitors (ChemMedChem 7/2010)

S. Laufer, C. Bracht, W. Albrecht, 2010 .

Biological Evaluation and Structural Determinants of p38α Mitogen‐Activated‐Protein Kinase and c‐Jun‐N‐Terminal Kinase 3 Inhibition by Flavonoids

S. Laufer, P. Koch, I. Merfort, 2010, Chembiochem : a European journal of chemical biology.