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Synthesis, structure and investigations of tuberculosis inhibition activities of new 4‐methyl‐1‐substituted‐1<i>H</i>‐1,2,4‐triazole‐5(4<i>H</i>)‐thione
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Citations
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References
2008
Year
Organic ChemistryAntimicrobial ChemotherapyChemistryBacterial PathogensPharmaceutical ChemistryMedicinal ChemistryAntimicrobial ResistanceAntimicrobial Drug DiscoveryTuberculosis Inhibition ActivitiesNew 4‐Methyl‐1‐substituted‐1TuberculosisAntibacterial AgentAntimicrobial CompoundFood PreservativesPharmacologyMycobacterium SmegmatisAntimicrobial SusceptibilityAntibioticsNatural SciencesReaction AminomethylationMycobacterium PhleiMicrobiologyMedicineSynthetic ChemistryDrug Discovery
Abstract magnified image By the reaction aminomethylation, chloromethylation and acylation of 4‐methyl‐4 H ‐1,2,4‐triazole‐3‐thiol, 4‐methyl‐1‐substituted‐1 H ‐1,2,4‐triazole‐5(4 H )‐thione 1‐8 were obtained. Molecular structure of the obtained compounds was confirmed by an elemental analysis, IR, 1 H NMR and 13 C NMR spectra and additionally by X‐ray analysis for 2. Six new compounds 1,2,4‐7 were tested for antibacterial activity against Mycobacterium smegmatis, Mycobacterium phlei and avirulent strain Mycobacterium H 37 Ra .
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