Department of Pharmacy, Faculty of Health Sciences, University of Brasília, Brasília 70910-900, DF, Brazil.
Computational Chemistry Laboratory, Institute of Chemistry, University of Brasília, Brasília 70910-900, DF, Brazil.
Molecules. 2024 Sep 8;29(17):4254. doi: 10.3390/molecules29174254.
Four afatinib derivatives were designed and modeled. These derivatives were compared to the known tyrosine-kinase inhibitors in treating Chronic Myeloid Leukemia, i.e., imatinib and ponatinib. The molecules were evaluated through computational methods, including docking studies, the non-covalent interaction index, Electron Localization and Fukui Functions, in silico ADMET analysis, QTAIM, and Heat Map analysis. The AFA(IV) candidate significantly increases the score value compared to afatinib. Furthermore, AFA(IV) was shown to be relatively similar to the ponatinib profile when evaluating a range of molecular descriptors. The addition of a methylpiperazine ring seems to be well distributed in the structure of afatinib when targeting the BCR-ABL enzyme, providing an important hydrogen bond interaction with the Asp381 residue of the DFG-switch of BCR-ABL active site residue and the AFA(IV) new chemical entities. Finally, in silico toxicity predictions show a favorable index, with some molecules presenting the loss of the irritant properties associated with afatinib in theoretical predictions.
设计并构建了四种阿法替尼衍生物。将这些衍生物与已知的酪氨酸激酶抑制剂伊马替尼和泊那替尼进行了比较,以治疗慢性髓性白血病。通过计算方法对分子进行了评估,包括对接研究、非共价相互作用指数、电子定域和 Fukui 函数、虚拟 ADMET 分析、QTAIM 和热图分析。与阿法替尼相比,AFA(IV)候选物的评分值显著增加。此外,在评估一系列分子描述符时,AFA(IV)的表现与泊那替尼相似。当靶向 BCR-ABL 酶时,添加一个甲基哌嗪环似乎可以很好地分布在阿法替尼的结构中,为 DFG 开关的 Asp381 残基和 BCR-ABL 活性位点残基提供重要的氢键相互作用。最后,虚拟毒性预测显示出有利的指数,一些分子在理论预测中表现出失去了与阿法替尼相关的刺激性特性。