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During the course of our investigations in the field of azole antimicrobial agents, we have identified
BM212 a pyrrole derivative with good
in vitro activity against
mycobacteria and
candidae. These findings prompted us to prepare new pyrrole derivatives
2–6 in the hope of increasing the activity. The microbiological data showed intersting
in vitro activity against
Mycobacterium tuberculosis and atypical mycobacteria.
New pyrrole derivatives, analogs of
BM212, were synthesized and tested against
M. tuberculosis and atypical mycobacteria. They showed an intersting activity.
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