Department of Biophysics and Neurobiology, Wroclaw Medical University, 50-368 Wrocław, Poland.
Molecules. 2021 Aug 29;26(17):5242. doi: 10.3390/molecules26175242.
Phenothiazines are known as synthetic antipsychotic drugs that exhibit a wide range of biological effects. Their properties result from the structure and variability of substituents in the heterocyclic system. It is known that different quantum chemical properties have a significant impact on drug behavior in the biological systems. Thus, due to the diversity in the chemical structure of phenothiazines as well as other drugs containing heterocyclic systems, quantum chemical calculations provide valuable methods in predicting their activity. In our study, DFT computations were applied to show some thermochemical parameters (bond dissociation enthalpy-BDE, ionization potential-IP, proton dissociation enthalpy-PDE, proton affinity-PA, and electrontransfer enthalpy-ETE) describing the process of releasing the hydrogen/proton from the hydroxyl group in the side chain of four 2-(trifluoromethyl)phenothiazine (TFMP) derivatives and fluphenazine (FLU). Additional theoretical analysis was carried out based on QTAIM theory. The results allowed theoretical determination of the ability of compounds to scavenge free radicals. In addition, the intramolecular hydrogen bond (H-bond) between the H-atom of the hydroxyl group and the N-atom located in the side chain of the investigated compounds has been identified and characterized.
吩噻嗪类药物是一类已知的合成抗精神病药物,具有广泛的生物学效应。它们的性质源于杂环系统中取代基的结构和可变性。已知不同的量子化学性质对药物在生物系统中的行为有重大影响。因此,由于吩噻嗪类药物以及其他含有杂环系统的药物的化学结构多样性,量子化学计算为预测其活性提供了有价值的方法。在我们的研究中,应用密度泛函理论(DFT)计算来展示一些描述从侧链中释放氢/质子的过程的热化学参数(键离解焓-BDE、电离势-IP、质子离解焓-PDE、质子亲合势-PA 和电子转移焓-ETE),在四个 2-(三氟甲基)吩噻嗪(TFMP)衍生物和氟奋乃静(FLU)。基于 QTAIM 理论进行了额外的理论分析。结果允许从理论上确定化合物清除自由基的能力。此外,还确定并表征了研究化合物中侧链上的羟基 H 原子与 N 原子之间的分子内氢键(H 键)。