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European Journal of Medicinal Chemistry|April 16, 2015
Exploring the chemical space of ureidothiophene-2-carboxylic acids as inhibitors of the quorum sensing enzyme PqsD from Pseudomonas aeruginosaJ Henning Sahner, Martin Empting, Ahmed Kamal, et al.
Journal of Enzyme Inhibition and Medicinal Chemistry|January 15, 2005
Evaluation of cell permeation of a potent 5alpha-reductase inhibitor using MALDI-TOF MSSonal Mathur, Franck Picard, Ulrich Dossou, et al.
Bioorganic & Medicinal Chemistry|September 11, 2008
CYP19 (aromatase): exploring the scaffold flexibility for novel selective inhibitorsSabrina Castellano, Giorgio Stefancich, Rino Ragno, et al.
Future Medicinal Chemistry|February 23, 2016
Design and synthesis of novel flexible ester-containing analogs of tamoxifen and their evaluation as anticancer agentsNehal H Elghazawy, Mathias Engel, Rolf W Hartmann, et al.
Journal of Medicinal Chemistry|March 4, 2016
Exploiting the Chromone Scaffold for the Development of Inhibitors of Corticosteroid BiosynthesisSilvia Gobbi, Qingzhong Hu, Christina Zimmer, et al.
Journal of Medicinal Chemistry|June 6, 2014
Novel pyridyl- or isoquinolinyl-substituted indolines and indoles as potent and selective aldosterone synthase inhibitorsLina Yin, Qingzhong Hu, Juliette Emmerich, et al.
Chembiochem : a European Journal of Chemical Biology|September 27, 2012
Mutation in elongation factor G confers resistance to the antibiotic argyrin in the opportunistic pathogen Pseudomonas aeruginosaPiotr Bielecki, Peer Lukat, Kristina Hüsecken, et al.
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