During the search of novel antitubercular drugs related to BM212, new diarylpyrroles were designed and synthesized on the basis of a structure–activity relationship analysis of many pyrroles previously described by us. Among them, 1-(4-fluorophenyl)-2-ethyl-3-(thiomorpholin-4-yl)methyl-5-(4-methyl-phenyl)-1H pyrrole(2b) proved to be particularly active, with a minimum inhibitory concentration (MIC, expressed as mg/mL) and a protection index (PI) better than or comparable to those of reference compounds. Also the remaining compounds were very active, although their MIC and PI were in general lower than those of their parent 2-methyl analogues.

1,5-Diaryl-2-ethyl pyrrole derivatives as antimycobacterial agents: design, synthesis, and microbiological evaluation.

DE ROSSI, EDDA;
2009

Abstract

During the search of novel antitubercular drugs related to BM212, new diarylpyrroles were designed and synthesized on the basis of a structure–activity relationship analysis of many pyrroles previously described by us. Among them, 1-(4-fluorophenyl)-2-ethyl-3-(thiomorpholin-4-yl)methyl-5-(4-methyl-phenyl)-1H pyrrole(2b) proved to be particularly active, with a minimum inhibitory concentration (MIC, expressed as mg/mL) and a protection index (PI) better than or comparable to those of reference compounds. Also the remaining compounds were very active, although their MIC and PI were in general lower than those of their parent 2-methyl analogues.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11571/202595
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