BetterScholar BetterScholar
9
Role
Title
Level Year L/R
๐Ÿœ 17ฮฒ-Hydroxysteroid dehydrogenases (17ฮฒ-HSDs) as therapeutic targets: Protein structures, functions, and recent progress in inhibitor development
13 auth. S. Marchais-Oberwinkler, C. Henn, G. Mรถller, T. Klein, M. Negri, Alexander Oster, A. Spadaro, R. Werth, M. Wetzel, Kuiying Xu, ... Martin Frotscher, R. Hartmann, J. Adamski
7 2011
7
๐Ÿœ
๐Ÿœ Design, synthesis, biological evaluation and pharmacokinetics of bis(hydroxyphenyl) substituted azoles, thiophenes, benzenes, and aza-benzenes as potent and selective nonsteroidal inhibitors of 17beta-hydroxysteroid dehydrogenase type 1 (17beta-HSD1).
10 auth. Emmanuel Bey, S. Marchais-Oberwinkler, R. Werth, M. Negri, Yaseen A. Al-Soud, Patricia Kruchten, ... Alexander Oster, Martin Frotscher, B. Birk, R. Hartmann
6 2008
6
๐Ÿœ
๐Ÿœ Synthesis, biological evaluation and molecular modelling studies of methyleneimidazole substituted biaryls as inhibitors of human 17alpha-hydroxylase-17,20-lyase (CYP17). Part I: Heterocyclic modifications of the core structure.
14 auth. Carsten Jagusch, M. Negri, Ulrike E. Hille, Qingzhong Hu, M. Bartels, Kerstin Jahn-Hoffmann, Mariano A E Pinto-Bazurco Mendieta, Barbara Rodenwaldt, U. Mรผllerโ€Vieira, D. Schmidt, ... Thomas Lauterbach, M. Recanatini, A. Cavalli, R. Hartmann
6 2008
6
๐Ÿœ
๐Ÿœ New insights into the SAR and binding modes of bis(hydroxyphenyl)thiophenes and -benzenes: influence of additional substituents on 17beta-hydroxysteroid dehydrogenase type 1 (17beta-HSD1) inhibitory activity and selectivity.
11 auth. Emmanuel Bey, S. Marchais-Oberwinkler, M. Negri, Patricia Kruchten, Alexander Oster, T. Klein, ... A. Spadaro, R. Werth, Martin Frotscher, B. Birk, R. Hartmann
6 2009
6
๐Ÿœ
๐Ÿœ Novel aldosterone synthase inhibitors with extended carbocyclic skeleton by a combined ligand-based and structure-based drug design approach.
9 auth. S. Lucas, Ralf Heim, M. Negri, I. Antes, C. Ries, K. Schewe, ... A. Bisi, S. Gobbi, R. Hartmann
6 2008
6
๐Ÿœ
๐Ÿœ Imidazolylmethylbenzophenones as highly potent aromatase inhibitors.
9 auth. S. Gobbi, A. Cavalli, M. Negri, K. Schewe, F. Belluti, Lorna Piazzi, ... R. Hartmann, M. Recanatini, A. Bisi
6 2007
6
๐Ÿœ
๐Ÿœ Novel CYP17 inhibitors: synthesis, biological evaluation, structure-activity relationships and modelling of methoxy- and hydroxy-substituted methyleneimidazolyl biphenyls.
8 auth. Ulrike E. Hille, Qingzhong Hu, Carsten A. Vock, M. Negri, M. Bartels, U. Mรผllerโ€Vieira, ... Thomas Lauterbach, R. Hartmann
6 2009
6
๐Ÿœ
๐Ÿฌ Synthesis, biological evaluation, and molecular modeling of abiraterone analogues: novel CYP17 inhibitors for the treatment of prostate cancer.
Mariano A E Pinto-Bazurco Mendieta, M. Negri, Carsten Jagusch, U. Mรผllerโ€Vieira, Thomas Lauterbach, R. Hartmann
5 2008
5
๐Ÿฌ
๐Ÿฌ Fine-tuning the selectivity of aldosterone synthase inhibitors: structure-activity and structure-selectivity insights from studies of heteroaryl substituted 1,2,5,6-tetrahydropyrrolo[3,2,1-ij]quinolin-4-one derivatives.
S. Lucas, M. Negri, Ralf Heim, Christina Zimmer, R. Hartmann
5 2011
5
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