Reference : Synthesis and biological activity of diaryl ether inhibitors of malarial enoyl acyl c...
Scientific journals : Article
Life sciences : Biochemistry, biophysics & molecular biology
http://hdl.handle.net/10993/16788
Synthesis and biological activity of diaryl ether inhibitors of malarial enoyl acyl carrier protein reductase. Part 2: 2'-substituted triclosan derivatives.
English
Freundlich, Joel S. [> >]
Yu, Min [> >]
Lucumi Moreno, Edinson mailto [University of Luxembourg > Luxembourg Centre for Systems Biomedicine (LCSB) >]
Kuo, Mack [> >]
Tsai, Han-Chun [> >]
Valderramos, Juan-Carlos [> >]
Karagyozov, Luchezar [> >]
Jacobs, William R. Jr [> >]
Schiehser, Guy A. [> >]
Fidock, David A. [> >]
Jacobus, David P. [> >]
Sacchettini, James C. [> >]
2006
Bioorganic & Medicinal Chemistry Letters
16
8
2163-9
Yes
0960-894X
England
[en] Animals ; Antimalarials/chemical synthesis/pharmacology ; Crystallography, X-Ray ; Drug Resistance, Microbial ; Enoyl-(Acyl-Carrier-Protein) Reductase (NADH)/antagonists & inhibitors ; Ethers/antagonists & inhibitors ; Plasmodium falciparum/drug effects ; Structure-Activity Relationship ; Triclosan/analogs & derivatives/chemistry
[en] 2'-Substituted analogs of triclosan have been synthesized to target inhibition of the key malarial enzyme Plasmodium falciparum enoyl acyl carrier protein reductase (PfENR). Many of these compounds exhibit good potency (EC50<500 nM) against in vitro cultures of drug-resistant and drug-sensitive strains of the P. falciparum parasite and modest (IC50=1-20 microM) potency against purified PfENR enzyme. Compared to triclosan, this survey of 2'-substituted derivatives has afforded gains in excess of 20- and 30-fold versus the 3D7 and Dd2 strains of parasite, respectively.
Researchers ; Professionals ; Students
http://hdl.handle.net/10993/16788

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