Synthesis, Insilico and Antibacterial Activity Studies of Substituted Dihydro-1, 2-Oxazole Benzopyran-2-One Hybrids

Alphonsus D’souza

Department of Chemistry, St. Philomena’s College (Autonomous) Mysuru-560001, Karnataka, India.

Pankaj Kumar *

Department of Pharmaceutical Chemistry, Nitte (Deemed to be University), NGSM Institute of Pharmaceutical Sciences, Deralakatte, Mangaluru-575018, India.

Abhishek Kumar

Department of Pharmaceutical Chemistry, Nitte (Deemed to be University), NGSM Institute of Pharmaceutical Sciences, Deralakatte, Mangaluru-575018, India.

Soundarya M. Rai

Department of Pharmaceutical Chemistry, Nitte (Deemed to be University), NGSM Institute of Pharmaceutical Sciences, Deralakatte, Mangaluru-575018, India.

Prashant Nayak

Department of Pharmaceutics, Nitte (Deemed to be University), NGSM Institute of Pharmaceutical Sciences, Deralakatte, Mangaluru-575018, India.

*Author to whom correspondence should be addressed.


Abstract

A series of substituted dihydro-1, 2-oxazole benzopyran-2-one (SR1-SR6) were synthesized through the intermediate substituted benzopyran-2-one chalcones and were characterized using spectral analysis.   Compounds were docked with receptor DNA Gyrase B (PDB code: 5L3J) to know its interaction and binding energy; ranges -3.38 to -2.15 kcal/mol. Further these compounds were tested for antibacterial activity using tube dilution method and MIC values were observed; ranges 3.12 to 25 µg/ml. Compound 3-(5-(m-tolyl)-4,5-dihydroisoxazol-3-yl)-2H-chromen-2-one (SR3) showed the best interaction with binding energy -3.38 kcal/mol and antimicrobial activity having MIC 3.12 µg/ml.

GRAPHICAL ABSTRACT

Capture6.PNG

Keywords: Benzopyran-2-one, chalcones, DNA Gyrase B, antibacterial activity


How to Cite

D’souza, Alphonsus, Pankaj Kumar, Abhishek Kumar, Soundarya M. Rai, and Prashant Nayak. 2021. “Synthesis, Insilico and Antibacterial Activity Studies of Substituted Dihydro-1, 2-Oxazole Benzopyran-2-One Hybrids”. Journal of Pharmaceutical Research International 33 (35A):134-44. https://doi.org/10.9734/jpri/2021/v33i35A31882.

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