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Urease Inhibition Studies of New Benzimidazoles Containing Triazole Ring

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Abstract

A new series of benzimidazoles including triazole and thiosemicarbazide moieties was synthesized and their urease inhibition studies were evaluated according to the method of Van Slyke and Archibald. Especially triazole derivatives have effective inhibition activities between 0.04±0.026 and 0.26±0.042 µM IC50 values. The best antiurease activities with IC50 0.04±0.026 and 0.06±0.033 µM belongs to 5-[(5,6-dichloro-1H-benzimidazol-1-yl)methyl]-4-nitrophenyl-4H-1,2,4-triazole-3-thiol and 2-[(2-benzyl-5,6-dichloro-1H-benzimidazol-1-yl)acetyl]-N-(4-nitrophenyl)hydrazinecarbothioamide, respectively.

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Authors and Affiliations

  1. Department of Chemistry, Faculty of Arts and Sciences, Recep Tayyip Erdogan University, 53950, Rize, Turkey

    G. Akyüz & E. Menteşe

  2. Department of Nutrition and Dietetics, Faculty of Health Sciences, Karadeniz Technical University, 61000, Trabzon, Turkey

    B. Kahveci

Authors
  1. G. Akyüz
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  2. E. Menteşe
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  3. B. Kahveci
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Correspondence to G. Akyüz.

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Akyüz, G., Menteşe, E. & Kahveci, B. Urease Inhibition Studies of New Benzimidazoles Containing Triazole Ring. Russ J Gen Chem 93, 449–454 (2023). https://doi.org/10.1134/S1070363223020287

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  • DOI: https://doi.org/10.1134/S1070363223020287

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