Design and in silico screening of novel isoniazid-based Schiff base derivatives followed by synthesis and biological evaluation of the lead compound against Mycobacterium tuberculosis H37Rv
The findings suggest that isoniazid-based Schiff base derivatives represent a promising scaffold for the development of new antitubercular agents, with SLB-5 emerging as a promising candidate for further investigation.
Abstract
The development of new antitubercular agents is critically needed due to the rising incidence of drug-resistant Mycobacterium tuberculosis. In the present study, a series of isoniazid-based Schiff base derivatives was designed and evaluated using an integrated in silico approach. A virtual library comprising 30 compounds was designed and systematically screened. Based on an integrated computational screening strategy involving drug-likeness evaluation, absorption, distribution, metabolism, excretion, and toxicity (ADMET) profiling, Prediction of Activity Spectra for Substances (PASS) analysis, and molecular docking, the highest-ranked lead compound (SLB-5) was selected for synthesis, structural characterization, and biological evaluation. Molecular docking was performed against enoyl-acyl carrier protein reductase (InhA) of M. tuberculosis (PDB ID: 6EP8), identifying compounds with favorable predicted binding affinities ranging from − 8.7 to − 9.5 kcal/mol, which were more favorable than the docking score of isoniazid (− 5.8 kcal/mol). The selected lead compound, SLB-5, was synthesized via Schiff base condensation and characterized using Fourier-transform infrared spectroscopy (FT-IR), proton nuclear magnetic resonance (¹H NMR), and high-resolution mass spectrometry (HRMS), confirming the formation of the azomethine (–C=N–) linkage. The antitubercular activity of SLB-5 was evaluated against M. tuberculosis H37Rv using the Alamar Blue assay, demonstrating concentration-dependent growth inhibition. Overall, the findings suggest that isoniazid-based Schiff base derivatives represent a promising scaffold for the development of new antitubercular agents. The study demonstrates the utility of an integrated computational screening workflow for prioritizing lead compounds for synthesis and biological evaluation, with SLB-5 emerging as a promising candidate for further investigation.
Findings highlight the potential of benzisothiazole‐based hydrazide derivatives as promising scaffolds for the development of new antitubercular agents and suggest InhA as a potential molecular target.
V. Sharma, Arun Sharma, Ruchi Poria et al.· Chemical Biology and Drug De...· 0 citations
Tuberculosis remains a major global health burden, highlighting the urgent need for new therapeutic agents with improved efficacy and safety. In this study, a series of vanillin-derived biphenyl ether analogues inspired by the nimesulide scaffold was designed and synthesized as multifunctional candidates targeting tube...
S. R., V. B. Hacholli, Ł. Szeleszczuk et al.· Indonesian Journal of Chemis...· 0 citations
The designed compounds implied Lipinski's Rule of Five and exhibited acceptable pharmacokinetic characteristics, according to ADME prediction studies conducted using ADMET Lab 3.0 web server, the tailored compounds were synthesized and characterised by spectral methods.
Kanala Somasekhar Reddy· Natural Resources for Human...· 0 citations
The combination of virtual screening, ADME studies, and MD simulations enabled the identification of phytochemicals with promising interactions toward InhA, an established anti-TB target, and should be interpreted as preliminary evidence of target engagement rather than confirmed inhibitory activity or therapeutic effi...
D. Kumar, Bhoomika, Alka Khichi et al.· Current Computer - Aided Dru...· 0 citations
In vitro findings identified compounds 6a, 6m, and 6n as potent leads, exhibiting significant antimicrobial activity with minimum inhibitory concentration values ranging from 15 to 500 µg/mL and antioxidant activity with DPPH IC50 values of 6.35 ± 0.51 μM, respectively.
Preetesh Kumar Panda, S. Paidesetty, Alaka Sahoo et al.· Future Medicinal Chemistry· 0 citations
Benzothiazole and isatin scaffolds possess considerable biological importance and their molecular hybridization may provide a promising approach for enhancing anticonvulsant activity. The present study focused on the design, synthesis and evaluation of a novel series of 6-substituted-N'-(5-substituted-2-oxoindolin-3-yl...
Bhavana Dubey, Kuldeep Singh, Arun Kumar et al.· Asian Journal of Chemistry· 0 citations
We use cookies to run the site and, with your consent, for analytics and to show ads.
See our Cookie Policy.