Abstract:
Introduction: Tuberculosis still remains the major danger for people’s health in most of the countries. The treatment of this illness hasn’t had the expected results.Jt’s the best way to stop the spread of
the infection. The main reason of this defficiency is drug resistance and often multidrug resistance of
Mycobacterium tuberculosis to anti-tuberculosis drugs used in therapy. The study of new substances
with anti-tuberculosis activity and elaboration of new effective remedies could increaese the range of
anti-tuberculosis medicines.
Aims: The synthesized compounds to benzoic acid thioureides are of great scientific and practical
interest to elaborate the new effective drugs. The aim of this study was to determine the anti-tuberculosis
activity of synthesized to benzoic acid thioureides compounds.
Methods and results: Using the reference strain H37R of M.tuberculosis isolated from TB patients
there was made a study of invitro antituberculosis activity of N- (2-fenetilbenzoil) -N- (3.5diclorfenil)
- thioureiaina number of substances of class thioureidesacid2 -(2’-fenetil)- benzoic acid by determining
the minimum inhibitory concentration (MIC). Activity above the minimum inhibitory substance was
studied in the liquid medium (Middlebrook 7H9) and solid (Lowenstein-Jensen). To study the MIC of the
substance were used 0.2 ml suspensions H37R and wild strains of a turbidity 5CFU at each concentration
of the substance: 200 mg/ml, 50 mg/ml, 30mg/ml, lOmg/ml, 7mg/mland 4mg/ml. The MICof of the
substance synthesized N-(2-fenetilbenzoil)-N-(3.5diclorfenil)-thioureia was established on lOmg/ml.
