. Compound 3c retained bactericidal activity under nutrient-starvation conditions and outperformed isoniazid (INH) in a dormancy model. Cytotoxicity assays in HepG2 and Vero E6 cells showed low toxicity (IC₅₀ > 100 μM). These findings identify 3c as a promising lead scaffold for anti-TB drug development.
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Paulo Fernando da Silva Santos-Júnior
Valnês S. Rodrigues-Junior
Monalisa Silva
Bioorganic & Medicinal Chemistry Letters
Universidade Federal do Rio Grande do Norte
Pontifícia Universidade Católica do Rio Grande do Sul
Universidade Federal da Paraíba
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Santos-Júnior et al. (Fri,) studied this question.
www.synapsesocial.com/papers/69fd7e42bfa21ec5bbf067df — DOI: https://doi.org/10.1016/j.bmcl.2026.130679