Novel small molecule inhibitors targeting the “switch region” of bacterial RNAP: structure-based optimization of a virtual screening hit
…, M Groh, M Negri, J Haupenthal, RW Hartmann
Index: Sahner, J. Henning; Groh, Matthias; Negri, Matthias; Haupenthal, Joerg; Hartmann, Rolf W. European Journal of Medicinal Chemistry, 2013 , vol. 65, p. 223 - 231
Full Text: HTML
Citation Number: 19
Abstract
Abstract Rising resistance against current antibiotics necessitates the development of antibacterial agents with alternative targets. The “switch region” of RNA polymerase (RNAP), addressed by the myxopyronins, could be such a novel target site. Based on a hit candidate discovered by virtual screening, a small library of 5-phenyl-3-ureidothiophene-2-carboxylic acids was synthesized resulting in compounds with increased RNAP inhibition. Hansch ...
Related Articles:
[Le Foulon, Francois-Xavier; Braud, Emmanuelle; Fabis, Frederic; Lancelot, Jean-Charles; Rault, Sylvain Tetrahedron, 2003 , vol. 59, # 50 p. 10051 - 10057]