Synthesis of Competitive and Noncompetitive Inhibitors of Alpha‐Glucosidase and Anticancer Agents
Imidazoles and phenylthiazoles are an important class of heterocycles that demonstrate a wide range of biological activities against various types of cancers, diabetes mellitus and pathogenic microorganisms. The heterocyclic structure having oxothiazolidine moiety is an important scaffold present in...
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Veröffentlicht in: | Chemistry & biodiversity 2024-05, Vol.21 (5), p.e202301399-n/a |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Imidazoles and phenylthiazoles are an important class of heterocycles that demonstrate a wide range of biological activities against various types of cancers, diabetes mellitus and pathogenic microorganisms. The heterocyclic structure having oxothiazolidine moiety is an important scaffold present in various drugs, with potential for enzyme inhibition. In an effort to discover new heterocyclic compounds, we synthesized 26 new 4,5‐diphenyl‐1H‐imidazole, phenylthiazole, and oxothiazolidine heterocyclic analogues that demonstrated potent α‐glucosidase inhibition and anticancer activities. Majority of the compounds noncompetitively inhibited α‐glucosidase except for two that exhibited competitive inhibition of the enzyme. Docking results suggested that the noncompetitive inhibitors bind to an apparent allosteric site on the enzyme located in the vicinity of the active site. Additionally, the analogues also exhibited significant activity against various types of cancers including non‐small lung cancer. Since tubulin protein plays an important role in the pathogenesis of non‐small lung cancer, molecular docking with one of the target compounds provided important clues to its binding mode. The current work on imidazoles and phenylthiazole derivatives bears importance for designing of new antidiabetic and anticancer drugs. |
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ISSN: | 1612-1872 1612-1880 |
DOI: | 10.1002/cbdv.202301399 |