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针对 COX-2/15-LOX 双重抑制的新型喹啉杂合体:设计、合成、SAR 和组织病理学研究。

Tailored quinoline hybrids as promising COX-2/15-LOX dual inhibitors endowed with diverse safety profile: Design, synthesis, SAR, and histopathological study.

机构信息

Department of Pharmaceutical Organic Chemistry, Faculty of Pharmacy, Al-Azhar University, Assiut 71524, Egypt.

Department of Pharmaceutical Organic Chemistry, Faculty of Pharmacy, Al-Azhar University, Assiut 71524, Egypt; Department of Basic Medical and Dental Sciences, Faculty of Dentistry, Zarqa University, Zarqa 13110, Jordan.

出版信息

Bioorg Chem. 2024 Apr;145:107244. doi: 10.1016/j.bioorg.2024.107244. Epub 2024 Feb 27.

Abstract

Complications of the worldwide use of non-steroidal anti-inflammatory drugs (NSAIDs) sparked scientists to design novel harmless alternatives as an urgent need. So, a unique hybridization tactic of quinoline/pyrazole/thioamide (4a-c) has been rationalized and synthesized as potential COX-2/15-LOX dual inhibitors, utilizing relevant reported studies on these pharmacophores. Moreover, we extended these preceding hybrids into more varied functionality, bearing crucial thiazole scaffolds(5a-l). All the synthesized hybrids were evaluatedin vitroas COX-2/15-LOX dual inhibitors. Initially, series4a-cexhibited significant potency towards 15-LOX inhibition (IC = 5.454-4.509 μM) compared to meclofenamate sodium (IC = 3.837 μM). Moreover, they revealed reasonable inhibitory activities against the COX-2 enzyme in comparison to celecoxib.Otherwise, conjugates 5a-ldisclosed marked inhibitory activity against 15-LOX and strong inhibitory to COX-2. In particular, hybrids5d(IC = 0.239 μM, SI = 8.95), 5h(IC = 0.234 μM, SI = 20.35) and 5l (IC = 0.201 μM, SI = 14.42) revealed more potency and selectivity outperforming celecoxib (IC = 0.512 μM, SI = 4.28). In addition, the most potentcompounds, 4a, 5d, 5h, and 5l have been elected for further in vivoevaluation and displayed potent inhibition of edema in the carrageenan-induced rat paw edema test that surpassed indomethacin. Further, compounds5d, 5h, and 5l decreased serum inflammatory markers including oxidative biomarkersiNO, and pro-inflammatory mediators cytokines like TNF-α, IL-6, and PGE. Ulcerogenic liability for tested compounds demonstrated obvious gastric mucosal safety. Furthermore, a histopathological study for compound 5l suggested a confirmatory comprehensive safety profile for stomach, kidney, and heart tissues. Docking and drug-likeness studies offered a good convention with the obtained biological investigation.

摘要

非甾体抗炎药(NSAIDs)在全球范围内使用所产生的并发症促使科学家们迫切需要设计新型无害替代品。因此,利用相关文献报道的这些药效团,我们合理化并合成了具有潜在 COX-2/15-LOX 双重抑制作用的独特喹啉/吡唑/硫代酰胺(4a-c)杂化策略。此外,我们将这些前体杂化物扩展为更具多样性的功能,带有关键的噻唑支架(5a-l)。所有合成的杂化物均在体外作为 COX-2/15-LOX 双重抑制剂进行评估。最初,与甲氯芬那酸(IC=3.837μM)相比,系列 4a-c 对 15-LOX 抑制具有显著的效力(IC=5.454-4.509μM)。此外,与塞来昔布相比,它们对 COX-2 酶也表现出合理的抑制活性。另一方面,5a-l 类化合物对 15-LOX 具有显著的抑制活性,并对 COX-2 具有强抑制作用。特别是,杂化物 5d(IC=0.239μM,SI=8.95)、5h(IC=0.234μM,SI=20.35)和 5l(IC=0.201μM,SI=14.42)显示出更强的效力和选择性,优于塞来昔布(IC=0.512μM,SI=4.28)。此外,选择最有效的化合物 4a、5d、5h 和 5l 进行进一步的体内评估,并在角叉菜胶诱导的大鼠足肿胀试验中显示出强大的抑制水肿作用,超过了吲哚美辛。此外,化合物 5d、5h 和 5l 降低了血清炎症标志物,包括氧化生物标志物 iNO 和促炎介质细胞因子 TNF-α、IL-6 和 PGE。测试化合物的致溃疡性表明对胃黏膜具有明显的安全性。此外,化合物 5l 的组织病理学研究表明,它对胃、肾和心脏组织具有全面的安全性。对接和药物相似性研究与获得的生物学研究结果相符。

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