Mumthaj A, Umadevi M, Kesavan Mookkandi Palsamy, Ravi Lokesh, Bhaskar R
PG Research Department of Chemistry, Nehru Memorial College (Autonomous), , Puthanampatti, (Affiliated to Bharathidasan University), 626 002, Tiruchirappalli, Tamil Nadu, India.
Department of Chemistry, Hajee Karutha Rowther Howdia College (Autonomous), 625 533, Uthamapalayam, Tamil Nadu, India.
J Fluoresc. 2024 Dec 18. doi: 10.1007/s10895-024-04081-1.
The research article details the synthesis of chalcone-chromone-based scaffolds via multicomponent reactions. These compounds were characterized using conventional spectroscopic methods, including NMR (H and C), FT-IR, and HR-MS. Among the synthesized scaffolds, AZBNPy stood out, exhibiting exceptional DNA and protein targeting capabilities with superior binding parameters. Molecular docking studies indicated that AZBNPy has potential as a potent anticancer agent and a probe for cancer cell imaging. The findings showed that AZBNPy effectively inhibited cell proliferation and induced cell death by targeting HER-2, PARP-2, and HFR in MCF-7 cells. Additionally, in vitro fluorescence imaging studies confirmed AZBNPy's specificity for cancer cell receptors, displaying strong fluorescence in human breast cancer tissues. The clinical application of AZBNPy as an optical imaging agent holds significant promise in aiding surgeons with the precise identification and removal of cancerous tissues, potentially improving patient outcomes and survival rates.
该研究文章详细介绍了通过多组分反应合成查尔酮-色酮基支架。这些化合物使用常规光谱方法进行了表征,包括核磁共振(氢和碳)、傅里叶变换红外光谱以及高分辨质谱。在合成的支架中,AZBNPy表现突出,具有出色的DNA和蛋白质靶向能力以及优异的结合参数。分子对接研究表明,AZBNPy有潜力成为一种有效的抗癌剂和癌细胞成像探针。研究结果显示,AZBNPy通过靶向MCF-7细胞中的HER-2、PARP-2和HFR有效抑制细胞增殖并诱导细胞死亡。此外,体外荧光成像研究证实了AZBNPy对癌细胞受体的特异性,在人乳腺癌组织中显示出强烈的荧光。AZBNPy作为光学成像剂的临床应用在帮助外科医生精确识别和切除癌组织方面具有重大前景,有可能改善患者的治疗效果和生存率。