Nesaragi Aravind R, Kamat Vinuta, Chapi Sharanappa, Guddappa Halligudra, T M Sharanakumar, Chandu Ala, Al-Zaqri Nabil, Palem Ramasubba Reddy, Murugesan Sankaranarayanan, Kumbar Vijay M
Department of Chemistry, Dayananda Sagar College of Engineering, Bangalore, India.
Department of Physics, B.M.S. College of Engineering, Bengaluru, Karnataka, India.
Arch Pharm (Weinheim). 2025 Apr;358(4):e202500055. doi: 10.1002/ardp.202500055.
Malononitrile, modified hydrazine, and quinoline aldehyde were combined in a one-pot reaction under microwave irradiation to create the medicinally significant family of heterocyclic scaffolds, quinoline, coumarin, thiazole, and pyrazole 4-carbonitrile derivatives with the help of green solvent as water. WELPSA (water extract of lemon peel-soaked ash) is used to speed up the reaction in a solvent-free environment, according to more environmentally friendly reaction protocols. This methodology offers several advantages like short reaction duration, green solvent synthesis, high yield, no need for chromatographic techniques, catalyst recyclability of up to five cycles, and so on. Synthesized derivatives were evaluated for anticancer potential against lung (A549) and breast cancer cell lines. Among the tested compounds, 4i and 4j exhibited remarkable anticancer activities. Further investigations using Annexin V staining and flow cytometry revealed that both compounds effectively induced apoptosis in A549 cancer cells. Compound 4i was subjected to molecular docking and dynamic studies to understand the molecular basis of their activity, which demonstrated a strong interaction with the target protein 1m17, providing insights into its mechanism of action. These findings highlight the potential of compounds 4i and 4j as promising candidates for anticancer drug development.
在微波辐射下,将丙二腈、改性肼和喹啉醛在水作为绿色溶剂的帮助下进行一锅法反应,以制备具有重要药用价值的杂环骨架家族,即喹啉、香豆素、噻唑和吡唑4-腈衍生物。根据更环保的反应方案,在无溶剂环境中使用柠檬皮浸泡灰分的水提取物(WELPSA)来加速反应。该方法具有几个优点,如反应时间短、绿色溶剂合成、产率高、无需色谱技术、催化剂可循环使用多达五个循环等。对合成的衍生物进行了针对肺癌(A549)和乳腺癌细胞系的抗癌潜力评估。在测试的化合物中,4i和4j表现出显著的抗癌活性。使用膜联蛋白V染色和流式细胞术的进一步研究表明,这两种化合物均能有效诱导A549癌细胞凋亡。对化合物4i进行了分子对接和动力学研究,以了解其活性的分子基础,结果表明它与靶蛋白1m17有强烈相互作用,从而深入了解其作用机制。这些发现突出了化合物4i和4j作为抗癌药物开发有前景候选物的潜力。