Hassan Mohd Zaheen, Osman Hasnah, Ali Mohamed Ashraf, Ahsan Mohamed Jawed
School of Chemical Sciences, Universiti Sains Malaysia, Minden, 11800 Penang, Malaysia; Department of Pharmaceutical Chemistry, Alwar Pharmacy College, M.I.A., Alwar, Rajasthan 301030, India.
School of Chemical Sciences, Universiti Sains Malaysia, Minden, 11800 Penang, Malaysia.
Eur J Med Chem. 2016 Nov 10;123:236-255. doi: 10.1016/j.ejmech.2016.07.056. Epub 2016 Jul 25.
Coumarins have received a considerable attention in the last three decades as a lead structures for the discovery of orally bioavailable non-peptidic antiviral agents. A lot of structurally diverse coumarins analogues were found to display remarkable array of affinity with the different molecular targets for antiviral agents and slight modifications around the central motif result in pronounced changes in its antiviral spectrum. This manuscript thoroughly reviews the design, discovery and structure-activity relationship studies of the coumarin analogues as antiviral agents focusing mainly on lead optimization and its development into clinical candidates.
在过去三十年里,香豆素作为发现口服生物可利用非肽类抗病毒药物的先导结构受到了广泛关注。许多结构多样的香豆素类似物被发现与抗病毒药物的不同分子靶点具有显著的亲和力,并且围绕中心基序的微小修饰会导致其抗病毒谱发生明显变化。本手稿全面综述了香豆素类似物作为抗病毒药物的设计、发现以及构效关系研究,主要聚焦于先导化合物优化及其发展为临床候选药物。