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The Journal of Steroid Biochemistry and Molecular Biology|May 12, 2009
Selective aldosterone synthase inhibitors reduce aldosterone formation in vitro and in vivoChristina Ries, Simon Lucas, Ralf Heim, et al.Chemmedchem|July 22, 2014
6-Hydroxybenzothiophene ketones: potent inhibitors of 17β-hydroxysteroid dehydrogenase type 1 (17β-HSD1) owing to favorable molecule geometry and conformational preorganizationParisa Miralinaghi, Christian Schmitt, Rolf W Hartmann, et al.The Journal of Steroid Biochemistry and Molecular Biology|July 26, 2002
Development of a test system for inhibitors of human aldosterone synthase (CYP11B2): screening in fission yeast and evaluation of selectivity in V79 cellsPeter B Ehmer, Matthias Bureik, Rita Bernhardt, et al.Angewandte Chemie (International Ed. in English)|December 17, 2013
Overcoming the unexpected functional inversion of a PqsR antagonist in Pseudomonas aeruginosa: an in vivo potent antivirulence agent targeting pqs quorum sensingCenbin Lu, Christine K Maurer, Benjamin Kirsch, et al.Archiv Der Pharmazie|April 26, 2012
Synthesis and biological evaluation of phenyl substituted 1H-1,2,4-triazoles as non-steroidal inhibitors of 17β-hydroxysteroid dehydrogenase type 2Yaseen A Al-Soud, Sandrine Marchais-Oberwinkler, Martin Frotscher, et al.Angewandte Chemie (International Ed. in English)|November 19, 2016
Metal-Free meta-Selective Alkyne Oxyarylation with Pyridine N-Oxides: Rapid Assembly of Metyrapone AnaloguesXiangyu Chen, Stefan A Ruider, Rolf W Hartmann, et al.Journal of Medicinal Chemistry|August 6, 2010
Replacement of imidazolyl by pyridyl in biphenylmethylenes results in selective CYP17 and dual CYP17/CYP11B1 inhibitors for the treatment of prostate cancerQingzhong Hu, Carsten Jagusch, Ulrike E Hille, et al.Journal of Medicinal Chemistry|March 3, 2012
Lead optimization of 17β-HSD1 inhibitors of the (hydroxyphenyl)naphthol sulfonamide type for the treatment of endometriosisClaudia Henn, Almuth Einspanier, Sandrine Marchais-Oberwinkler, et al.European Journal of Medicinal Chemistry|May 29, 2013
Novel small molecule inhibitors targeting the "switch region" of bacterial RNAP: structure-based optimization of a virtual screening hitJ Henning Sahner, Matthias Groh, Matthias Negri, et al.European Journal of Medicinal Chemistry|December 22, 2014
Heteroatom insertion into 3,4-dihydro-1H-quinolin-2-ones leads to potent and selective inhibitors of human and rat aldosterone synthaseCornelia M Grombein, Qingzhong Hu, Sabrina Rau, et al.Pageof 26