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Regioselective One-Pot Synthesis, Biological Activity and Molecular Docking Studies of Novel Conjugates N-(p-Aryltriazolyl)-1,5-benzodiazepin-2-ones as Potent Antibacterial and Antifungal Agents.


ABSTRACT: Novel 1,2,3-triazolo-linked-1,5-benzodiazepinones were designed and synthesized via a Cu(I)-catalyzed 1,3-dipolar alkyne-azide coupling reaction (CuAAC). The chemical structures of these compounds were confirmed by 1H NMR, 13C NMR, HMBC, HRMS, and elemental analysis. The compounds were screened for their in vitro antibacterial and antifungal activities. Several compounds exhibited good to moderate activities compared to those of established standard drugs. Furthermore, the binding interactions of these active analogs were confirmed through molecular docking.

SUBMITTER: Nsira A 

PROVIDER: S-EPMC9268147 | biostudies-literature | 2022 Jun

REPOSITORIES: biostudies-literature

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Regioselective One-Pot Synthesis, Biological Activity and Molecular Docking Studies of Novel Conjugates <i>N</i>-(p-Aryltriazolyl)-1,5-benzodiazepin-2-ones as Potent Antibacterial and Antifungal Agents.

Nsira Asma A   Mtiraoui Hasan H   Chniti Sami S   Al-Ghulikah Hanan H   Gharbi Rafik R   Msaddek Moncef M  

Molecules (Basel, Switzerland) 20220622 13


Novel 1,2,3-triazolo-linked-1,5-benzodiazepinones were designed and synthesized via a Cu(I)-catalyzed 1,3-dipolar alkyne-azide coupling reaction (CuAAC). The chemical structures of these compounds were confirmed by <sup>1</sup>H NMR, <sup>13</sup>C NMR, HMBC, HRMS, and elemental analysis. The compounds were screened for their in vitro antibacterial and antifungal activities. Several compounds exhibited good to moderate activities compared to those of established standard drugs. Furthermore, the  ...[more]

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