Adam Abdel Majid A, Saad Hosam A, Refat Moamen S, Hegab Mohamed S
Department of Chemistry, College of Science, Taif University, P.O. Box 11099, Taif 21944, Saudi Arabia.
Deanship of Supportive Studies (D.S.S.), Taif University, P.O. Box 11099, Taif 21944, Saudi Arabia.
J Mol Liq. 2022 Jul 1;357:119092. doi: 10.1016/j.molliq.2022.119092. Epub 2022 Apr 8.
COVID-19 is the disease caused by a novel coronavirus (CoV) named the severe acute respiratory syndrome coronavirus 2 (termed SARS coronavirus 2 or SARS-CoV-2). Since the first case reported in December 2019, infections caused by this novel virus have led to a continuous global pandemic that has placed an unprecedented burden on health, economic, and social systems worldwide. In response, multiple therapeutic options have been developed to stop this pandemic. One of these options is based on traditional corticosteroids, however, chemical modifications to enhance their efficacy remain largely unexplored. Obtaining additional insight into the chemical and physical properties of pharmacologically effective drugs used to combat COVID-19 will help physicians and researchers alike to improve current treatments and vaccines (i.e., Pfizer-BioNTech, AstraZeneca, Moderna, Janssen). Herein, we examined the charge-transfer properties of two corticosteroids used as adjunctive therapies in the treatment of COVID-19, hydrocortisone and dexamethasone, as donors with 2,3-dichloro-5,6-dicyano--benzoquinone as an acceptor in various solvents. We found that the examined donors reacted strongly with the acceptor in CHCl and CHCl solvents to create stable compounds with novel clinical potential.
新型冠状病毒肺炎(COVID-19)是由一种名为严重急性呼吸综合征冠状病毒2(简称SARS冠状病毒2或SARS-CoV-2)的新型冠状病毒引起的疾病。自2019年12月报告首例病例以来,这种新型病毒引起的感染已导致全球持续大流行,给全球的卫生、经济和社会系统带来了前所未有的负担。作为应对措施,已开发出多种治疗方案来阻止这场大流行。其中一种方案基于传统的皮质类固醇,然而,对其进行化学修饰以提高疗效在很大程度上仍未得到探索。深入了解用于对抗COVID-19的药理有效药物的化学和物理性质,将有助于医生和研究人员改进当前的治疗方法和疫苗(即辉瑞-生物科技公司、阿斯利康、莫德纳、杨森公司的疫苗)。在此,我们研究了在COVID-19治疗中用作辅助疗法的两种皮质类固醇——氢化可的松和地塞米松作为供体,与作为受体的2,3-二氯-5,6-二氰基-1,4-苯醌在各种溶剂中的电荷转移性质。我们发现,所研究的供体在氯仿和二氯甲烷溶剂中与受体发生强烈反应,生成具有新临床潜力的稳定化合物。