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Bioorg Med Chem Lett ; 25(8): 1799-1803, 2015 Apr 15.
Article in English | MEDLINE | ID: mdl-25736994

ABSTRACT

The worldwide threat from tuberculosis (TB) has resulted in great demand for new drugs, particularly those that can treat multidrug-resistant TB. We synthesized novel pleuromutilin derivatives with N-benzylamine side chain substituted at the C14 position and evaluated their activity in vitro against a virulent strain of Mycobacterium tuberculosis (H37Rv). The primary assay results showed that five compounds inhibited the H37Rv at 20µM, with a MIC of one of the analogues as low as 7.2µM.


Subject(s)
Antitubercular Agents/chemical synthesis , Antitubercular Agents/chemistry , Antitubercular Agents/pharmacology , Diterpenes/chemical synthesis , Diterpenes/chemistry , Diterpenes/pharmacology , Drug Design , Drug Resistance, Microbial , Microbial Sensitivity Tests , Mycobacterium tuberculosis/drug effects , Polycyclic Compounds , Structure-Activity Relationship , Pleuromutilins
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