| Literature DB >> 15050641 |
Johann Leban1, Stefano Pegoraro, Matthias Dormeyer, Michael Lanzer, Andrea Aschenbrenner, Bernd Kramer.
Abstract
The high throughput in silico screening of a virtual library into the structure of the P. falciparum lactate dehydrogenase (LDH) with the 4SCan technology yielded a series of biphenyl urea compounds. These were chemically optimized to a new structural class of potent antimalarial agents. The compounds did not inhibit plasmodium LDH enough to fully explain their potency. Therefore we conclude that an unknown mode of action may be the cause of the antimalarial activity.Entities:
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Year: 2004 PMID: 15050641 DOI: 10.1016/j.bmcl.2004.01.083
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823