2-Oxoindolin-thiazoline hybrids as scaffold-based therapeutics for T2DM-associated cognitive impairment: design, synthesis, in vitro and in silico studies
IF 3.597 Q2 Pharmacology, Toxicology and Pharmaceutics
Wesam S. Qayed, Mostafa A. Hassan, Halil Şenol, Parham Taslimi and Tarek Aboul-Fadl
{"title":"2-Oxoindolin-thiazoline hybrids as scaffold-based therapeutics for T2DM-associated cognitive impairment: design, synthesis, in vitro and in silico studies","authors":"Wesam S. Qayed, Mostafa A. Hassan, Halil Şenol, Parham Taslimi and Tarek Aboul-Fadl","doi":"10.1039/D5MD00628G","DOIUrl":null,"url":null,"abstract":"<p >Alzheimer's disease (AD) and type 2 diabetes mellitus (T2DM) are closely linked neurodegenerative and metabolic disorders, sharing overlapping pathological mechanisms. In this study, structure-based drug design combined with molecular hybridization strategies was employed to develop dual-acting compounds targeting both conditions. A series of twenty hybrid molecules, comprising 2-oxoindolin-3-thiosemicarbazones (<strong>3a–i</strong>) and thiazolines (<strong>4a–k</strong>) were successfully synthesized and characterized using spectroscopic techniques and elemental analysis. Biological evaluations demonstrated that compounds <strong>3d</strong> and <strong>3h</strong> exhibit potent inhibitory activity against α-glucosidase (α-Glu) and α-amylase (α-Amy), surpassing the efficacy of acarbose. These findings highlight their promising antidiabetic potential and support further investigation into their therapeutic relevance for AD and T2DM comorbidity (<strong>3d</strong> (α-glucosidase <em>K</em><small><sub>i</sub></small> = 41.41 ± 2.53 nM; α-amylase IC<small><sub>50</sub></small> = 1.25 ± 0.02 nM), <strong>3h</strong> (α-glucosidase <em>K</em><small><sub>i</sub></small> = 44.19 ± 2.41 nM; α-amylase IC<small><sub>50</sub></small> = 2.87 ± 0.16 nM and <strong>acrabose</strong> (α-glucosidase <em>K</em><small><sub>i</sub></small> = 101.20 ± 7.53, α-amylase IC<small><sub>50</sub></small> 9.73 ± 0.20). Furthermore, compounds <strong>3i</strong> and <strong>4i</strong> exhibited significantly higher inhibitory activity against acetylcholinesterase (AChE) and butyrylcholinesterase (BChE) compared to the reference drug tacrine. Notably, compound <strong>4i</strong> demonstrated exceptional multi-enzyme inhibition, with kinetic parameters indicating strong binding affinity: <strong>3i</strong> (AChE <em>K</em><small><sub>i</sub></small> = 59.71 ± 2.24 nM; BChE <em>K</em><small><sub>i</sub></small> = 8.43 ± 0.97 nM), <strong>4i</strong> (AChE <em>K</em><small><sub>i</sub></small> = 53.31 ± 1.74 nM; BChE <em>K</em><small><sub>i</sub></small> = 10.72 ± 2.19 nM), and <strong>tacrine</strong> (AChE <em>K</em><small><sub>i</sub></small> = 132.35 ± 5.90 nM; BChE <em>K</em><small><sub>i</sub></small> = 137.42 ± 4.01 nM). Molecular docking and dynamics simulations corroborated these findings by revealing stable and favorable interactions within the active sites of both enzymes. Additionally, <em>in silico</em> ADME profiling indicated desirable pharmacokinetic properties, further supporting the therapeutic potential of these compounds as dual-action agents for the management of Alzheimer's disease and type 2 diabetes mellitus.</p>","PeriodicalId":88,"journal":{"name":"MedChemComm","volume":" 1","pages":" 317-342"},"PeriodicalIF":3.5970,"publicationDate":"2025-11-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"MedChemComm","FirstCategoryId":"1085","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2026/md/d5md00628g","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"Pharmacology, Toxicology and Pharmaceutics","Score":null,"Total":0}
引用次数: 0
Abstract
Alzheimer's disease (AD) and type 2 diabetes mellitus (T2DM) are closely linked neurodegenerative and metabolic disorders, sharing overlapping pathological mechanisms. In this study, structure-based drug design combined with molecular hybridization strategies was employed to develop dual-acting compounds targeting both conditions. A series of twenty hybrid molecules, comprising 2-oxoindolin-3-thiosemicarbazones (3a–i) and thiazolines (4a–k) were successfully synthesized and characterized using spectroscopic techniques and elemental analysis. Biological evaluations demonstrated that compounds 3d and 3h exhibit potent inhibitory activity against α-glucosidase (α-Glu) and α-amylase (α-Amy), surpassing the efficacy of acarbose. These findings highlight their promising antidiabetic potential and support further investigation into their therapeutic relevance for AD and T2DM comorbidity (3d (α-glucosidase Ki = 41.41 ± 2.53 nM; α-amylase IC50 = 1.25 ± 0.02 nM), 3h (α-glucosidase Ki = 44.19 ± 2.41 nM; α-amylase IC50 = 2.87 ± 0.16 nM and acrabose (α-glucosidase Ki = 101.20 ± 7.53, α-amylase IC50 9.73 ± 0.20). Furthermore, compounds 3i and 4i exhibited significantly higher inhibitory activity against acetylcholinesterase (AChE) and butyrylcholinesterase (BChE) compared to the reference drug tacrine. Notably, compound 4i demonstrated exceptional multi-enzyme inhibition, with kinetic parameters indicating strong binding affinity: 3i (AChE Ki = 59.71 ± 2.24 nM; BChE Ki = 8.43 ± 0.97 nM), 4i (AChE Ki = 53.31 ± 1.74 nM; BChE Ki = 10.72 ± 2.19 nM), and tacrine (AChE Ki = 132.35 ± 5.90 nM; BChE Ki = 137.42 ± 4.01 nM). Molecular docking and dynamics simulations corroborated these findings by revealing stable and favorable interactions within the active sites of both enzymes. Additionally, in silico ADME profiling indicated desirable pharmacokinetic properties, further supporting the therapeutic potential of these compounds as dual-action agents for the management of Alzheimer's disease and type 2 diabetes mellitus.
阿尔茨海默病(AD)和2型糖尿病(T2DM)是密切相关的神经退行性和代谢性疾病,具有重叠的病理机制。在本研究中,采用基于结构的药物设计结合分子杂交策略来开发针对这两种情况的双作用化合物。成功合成了由2-氧吲哚-3-硫代氨基脲(3a-i)和噻唑啉(4a-k)组成的20个杂化分子,并利用光谱技术和元素分析对其进行了表征。生物学评价表明,化合物3d和3h对α-葡萄糖苷酶(α-Glu)和α-淀粉酶(α-Amy)具有较强的抑制活性,优于阿卡波糖。这些发现突出了它们具有良好的降糖潜力,并支持进一步研究它们与AD和T2DM合病的治疗相关性(3d (α-葡萄糖苷酶ki = 41.41±2.53 nM; α-淀粉酶IC50 = 1.25±0.02 nM), 3h (α-葡萄糖苷酶ki = 44.19±2.41 nM; α-淀粉酶IC50 = 2.87±0.16 nM)和葡萄糖酶(α-葡萄糖苷酶ki = 101.20±7.53,α-淀粉酶IC50 = 9.73±0.20)。此外,化合物3i和4i对乙酰胆碱酯酶(AChE)和丁基胆碱酯酶(BChE)的抑制活性明显高于参比药物他林。值得注意的是,化合物4i表现出特殊的多酶抑制作用,其动力学参数表明具有较强的结合亲和力:3i (AChE K i = 59.71±2.24 nM; BChE K i = 8.43±0.97 nM)、4i (AChE K i = 53.31±1.74 nM; BChE K i = 10.72±2.19 nM)和tacrine (AChE K i = 132.35±5.90 nM; BChE K i = 137.42±4.01 nM)。分子对接和动力学模拟通过揭示两种酶活性位点内稳定和有利的相互作用证实了这些发现。此外,计算机ADME分析显示了理想的药代动力学特性,进一步支持这些化合物作为治疗阿尔茨海默病和2型糖尿病的双重作用药物的治疗潜力。
期刊介绍:
Research and review articles in medicinal chemistry and related drug discovery science; the official journal of the European Federation for Medicinal Chemistry.
In 2020, MedChemComm will change its name to RSC Medicinal Chemistry. Issue 12, 2019 will be the last issue as MedChemComm.