Department of NEUROFARBA, Pharmaceutical and Nutraceutical Section, University of Florence, Sesto Fiorentino, Florence 50019, Italy.
Department of NEUROFARBA, Section of Pharmacology and Toxicology, Laboratory of Ocular and Neuropsychopharmacology (Braeye Lab), University of Florence, Viale Pieraccini 6, Florence 50139, Italy.
J Med Chem. 2024 Sep 26;67(18):16873-16898. doi: 10.1021/acs.jmedchem.4c01866. Epub 2024 Sep 16.
This study introduces a novel multitargeting strategy that combines carbonic anhydrase (CA) activators and cholinesterase (ChE) inhibitors to enhance cognitive functions. A series of tacrine-based derivatives with amine/amino acid moieties were synthesized and evaluated for their dual activity on brain CA isoforms and ChEs (AChE and BChE). Several derivatives, notably compounds , , , and , demonstrated potent CA activation, particularly of hCA II and VII, and strong ChE inhibition with subnanomolar to low nanomolar IC values. studies using a mouse model of social recognition memory showed that these derivatives significantly improved memory consolidation at doses 10-100 times lower than the reference compounds (either alone or in combination). Molecular modeling and ADMET predictions elucidated the compound binding modes and confirmed favorable pharmacokinetic and safety profiles. The findings suggest that dual modulation of CA and ChE activities is a promising strategy for treating cognitive deficits associated with neurodegenerative and psychiatric disorders.
本研究提出了一种新的多靶点策略,将碳酸酐酶(CA)激活剂和胆碱酯酶(ChE)抑制剂结合起来,以增强认知功能。合成了一系列基于他克林的衍生物,并带有胺/氨基酸部分,对其在脑 CA 同工酶和 ChE(AChE 和 BChE)上的双重活性进行了评估。一些衍生物,特别是化合物 、 、 、和 ,表现出对 hCA II 和 VII 的强大 CA 激活作用,以及对 ChE 的强烈抑制作用,IC 值低至纳摩尔。使用社交识别记忆的小鼠模型进行的研究表明,这些衍生物在剂量低至参考化合物(单独或联合使用)10-100 倍的情况下,可显著改善记忆巩固。分子建模和 ADMET 预测阐明了化合物的结合模式,并证实了有利的药代动力学和安全性特征。研究结果表明,CA 和 ChE 活性的双重调节是治疗与神经退行性和精神疾病相关的认知缺陷的一种有前途的策略。