College of Pharmacy, Chonnam National University, Gwangju 61186, Republic of Korea.
Infectious Diseases Therapeutic Research Center, Korea Research Institute of Chemical Technology (KRICT), Daejeon 34114, Republic of Korea.
Drug Discov Today. 2022 Jul;27(7):1895-1912. doi: 10.1016/j.drudis.2022.05.016. Epub 2022 May 21.
Cyclophilin A (CypA) is linked to diverse human diseases including viral infections. With the worldwide emergence of severe acute respiratory coronavirus 2 (SARS-CoV-2), drug repurposing has been highlighted as a strategy with the potential to speed up antiviral development. Because CypA acts as a proviral component in hepatitis C virus, coronavirus and HIV, its inhibitors have been suggested as potential treatments for these infections. Here, we review the structure of cyclosporin A and sanglifehrin A analogs as well as synthetic micromolecules inhibiting CypA; and we discuss their broad-spectrum antiviral efficacy in the context of the virus lifecycle.
亲环素 A(CypA)与多种人类疾病有关,包括病毒感染。随着严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)在全球范围内的出现,药物再利用已成为一种具有加速抗病毒药物开发潜力的策略。由于 CypA 作为丙型肝炎病毒、冠状病毒和 HIV 的促病毒成分,其抑制剂已被提议作为这些感染的潜在治疗方法。在这里,我们回顾了环孢菌素 A 和桑福来林 A 类似物以及抑制 CypA 的合成小分子的结构;并讨论了它们在病毒生命周期背景下的广谱抗病毒功效。