de Lima Fernanda Rodrigues, de Oliveira Viana Jéssika, de Castro Aleff Cruz, Cristiano Rodrigo, Perelló Marcia Alberton, Czeczot Alexia de Matos, Bizarro Cristiano Valim, Machado Pablo, Basso Luiz Augusto, Lima-Junior Claudio Gabriel, Rodrigues-Junior Valnês da Silva, Weber Karen Cacilda
Programa de Pós-Graduação em Química, Universidade Federal da Paraíba (UFPB), João Pessoa, Brazil.
National Institute of Science and Technology on Molecular Sciences-INCT-CiMol, João Pessoa, Brazil.
Chem Biol Drug Des. 2025 Jul;106(1):e70152. doi: 10.1111/cbdd.70152.
Tuberculosis (TB) remains a major global health threat, exacerbated by multidrug-resistant Mycobacterium tuberculosis (MTB) strains. The development of new anti-TB agents is crucial. In this study, 17 isatin derivatives synthesized by our research group were evaluated for their in vitro activity against MTB strains and the two most potent compounds were assessed for cytotoxicity. Additionally, molecular docking was performed against 22 MTB protein targets to explore possible mechanisms of action, and ADMET predictions were used to determine pharmacokinetic and pharmacodynamic suitability. Also, we investigated the activity of A15, A16, and A17 against two genetically characterized multidrug-resistant clinical isolates (PT-12 and PT-20). As a result, the compounds A16 and A17 exhibited the highest anti-TB activity (MIC = 10 μM for both). Inverse molecular docking indicated the enzyme enoyl-[acyl-carrier-protein] reductase as a potential biological target. Cytotoxicity assays confirmed that A16 and A17 were non-toxic, and ADMET predictions indicated suitable drug-like properties for anti-TB therapy. Notably, A16 and A17 showed inhibitory effects against drug-resistant MTB isolates, with minimum inhibitory concentrations (MICs) ranging from 10 to 20 μM, suggesting their potential to overcome resistance mechanisms linked to mutations in katG and rpoB. These findings highlight A16 and A17 as promising candidates for anti-TB agents, particularly against multidrug-resistant strains.
结核病(TB)仍然是全球主要的健康威胁,耐多药结核分枝杆菌(MTB)菌株使其情况更加恶化。开发新型抗结核药物至关重要。在本研究中,对我们研究小组合成的17种异吲哚酮衍生物进行了体外抗MTB菌株活性评估,并对两种最有效的化合物进行了细胞毒性评估。此外,针对22个MTB蛋白靶点进行了分子对接,以探索可能的作用机制,并利用ADMET预测来确定其药代动力学和药效学适用性。我们还研究了A15、A16和A17对两种基因特征明确的耐多药临床分离株(PT-12和PT-20)的活性。结果,化合物A16和A17表现出最高的抗结核活性(两者的MIC均为10μM)。反向分子对接表明烯酰-[酰基载体蛋白]还原酶是潜在的生物学靶点。细胞毒性试验证实A16和A17无毒,ADMET预测表明它们具有适合抗结核治疗的类药物特性。值得注意的是,A16和A17对耐药MTB分离株显示出抑制作用,最低抑菌浓度(MIC)范围为10至20μM,表明它们有可能克服与katG和rpoB基因突变相关的耐药机制。这些发现突出了A16和A17作为抗结核药物的有前景的候选物,特别是针对耐多药菌株。