European Journal of Chemistry

Synthesis, Type II diabetes inhibitory activity, antimicrobial evaluation, and docking studies of N'-arylidene-2-((7-methylbenzo[4,5]thiazolo[2,3-c] [1,2,4]triazol-3-yl)thio)acetohydrazides

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Published: Dec 31, 2022
DOI: https://doi.org/10.5155/eurjchem.13.4.426-434.2315
Keywords:
α-Amylase, Hydrazones, Benzothiazole, Docking studies, Acetohydrazide, Antimicrobial activity
Section
Research Article
Issue
Vol. 13 No. 4 (2022): December 2022
Dates
Received 2022-07-25
Accepted 2022-09-09
Published 2022-12-31
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Satbir Mor
Department of Chemistry, Guru Jambheshwar University of Science and Technology, Hisar-125001, Haryana, India
https://orcid.org/0000-0003-2114-0611
Suchita Sindhu
Department of Chemistry, Guru Jambheshwar University of Science and Technology, Hisar-125001, Haryana, India
https://orcid.org/0000-0002-3447-0831
Mohini Khatri
Department of Chemistry, Guru Jambheshwar University of Science and Technology, Hisar-125001, Haryana, India
https://orcid.org/0000-0002-8283-7167
Ravinder Punia
Department of Chemistry, Guru Jambheshwar University of Science and Technology, Hisar-125001, Haryana, India
https://orcid.org/0000-0001-5085-3376
Komal Jakhar
Department of Chemistry, Maharishi Dayanand University, Rohtak-124001, Haryana, India
https://orcid.org/0000-0003-3063-0655

Abstract

N'-Arylidene-2-((7-methylbenzo[4, 5]thiazolo[2,3-c][1, 2, 4]triazol-3-yl)thio)acetohydrazides (6a-j) were prepared by condensation of 2-((7-methylbenzo[4,5]thiazolo[2,3-c][1,2,4] triazol-3-yl)thio)acetohydrazide with appropriately substituted benzaldehydes in dry methanol and a catalytic amount of glacial acetic acid. The prepared compounds tested for in vitro Type II diabetes inhibition and antimicrobial (antibacterial and antifungal) activities employing α-amylase inhibition assay and the serial dilution method, respectively. Type II diabetes inhibitory assay results of all the tested derivatives revealed that precursor 3 (IC50 = 0.16 μM) and acetohydrazide 6i (IC50 = 0.38 μM) showed comparable activity with standard drug acarbose (IC50 = 0.15 μM). The derivatives 6i against B. subtilis and E. coli with MIC values of 0.0300 μmol/mL, compound 6c against S. aureus (MIC = 0.0312 μmol/mL) and compound 6e against P. aeruginosa (MIC = 0.0316 μmol/mL) exhibited remarkable antibacterial activity, however, compound 6b was found to be more active against the fungal strain C. albicans with MIC value of 0.0135 μmol/mL. All acetohydrazides (6a-j) showed greater potency against all strains tested than their precursors 1-4, which is also supported by the results of molecular docking analysis. Furthermore, no general trend for structure activity relationships was established for Type II diabetes inhibitory activity, nor antimicrobial activities of the tested hydrazones (6a-j).


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Mor, S.; Sindhu, S.; Khatri, M.; Punia, R.; Jakhar, K. Synthesis, Type II Diabetes Inhibitory Activity, Antimicrobial Evaluation, and Docking Studies of N’-Arylidene-2-(7-methylbenzo[4,5]thiazolo[2,3-C] [1,2,4]triazol-3-yl)thio)acetohydrazides. Eur. J. Chem. 2022, 13, 426-434.

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Supporting Agencies

Council of Scientific and Industrial Research (CSIR), CSIR No. 09/752(0060)/2016-EMR-I, New Delhi, India.
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