| Literature DB >> 30122226 |
Yan-Yan Wang1, Fang-Zhou Xu1, Yun-Ying Zhu2, Baoan Song3, Dexia Luo1, Gang Yu1, Shunhong Chen1, Wei Xue1, Jian Wu4.
Abstract
A series of pyrazolo[3,4-d]pyrimidine derivatives containing a Schiff base moiety were synthesized, characterised, and evaluated for their activity against tobacco mosaic virus (TMV). Biological assays indicated that several of the derivatives exhibited significant activity against TMV. In particularly, compounds 5y and 5aa displayed excellent inactivating activity against TMV, with half maximal effective concentration (EC50) values of 70.3 and 53.65 μg/mL, respectively, which were much better than that of ribavirin (150.45 μg/mL), and 5aa was superior to ningnanmycin (EC50 = 55.35 μg/mL). Interactions of compounds 5y and 5aa with TMV coat protein (TMV-CP) were investigated using microscale thermophoresis and molecular docking. Compounds 5y and 5aa displayed strong binding capability to TMV-CP with dissociation constant (Kd) values of 22.6 and 9.8 μM, respectively. These findings indicate that pyrazolo[3,4-d]pyrimidine derivatives containing a Schiff base may be potential antiviral agents.Entities:
Keywords: Antiviral activity; Molecular docking; Pyrazolo[3,4-d]pyrimidine; Schiff base
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Year: 2018 PMID: 30122226 DOI: 10.1016/j.bmcl.2018.06.049
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823