Cátedra de Química Medicinal, Universidad de Buenos Aires, Argentina.
Curr Med Chem. 2010;17(26):2933-55. doi: 10.2174/092986710792065036.
Viruses belonging to the Flaviviridae family cause clinically significant diseases in humans and animals. This family includes three genera: Pestivirus [including bovine viral diarrhea virus (BVDV)], Flavivirus [including yellow fever virus (YFV), dengue virus, and West Nile virus (WNV)], and Hepacivirus [including hepatitis C virus (HCV)]. BVDV is responsible for major losses in cattle, causing a range of clinical manifestations, and is also a problematic contaminant in the laboratory. Noncytopathic BVDV infection can remain unnoticed and infect laboratory cell lines through its presence in contaminated bovine serum used in cell culture. BVDV is considered to be a valuable surrogate virus model for identifying and characterizing antiviral agents to be used against HCV. In some aspects of viral replication, BVDV is more advantageous than the currently used HCV replicon systems. In this review, we report the design, synthesis, and activity against BVDV of a series of compounds assayed until now.
属于黄病毒科的病毒会导致人和动物的临床显著疾病。该科包括三个属:瘟病毒(包括牛病毒性腹泻病毒(BVDV))、黄病毒(包括黄热病病毒(YFV)、登革热病毒和西尼罗河病毒(WNV))和肝病毒(包括丙型肝炎病毒(HCV))。BVDV 是导致牛群重大损失的原因,引起多种临床表现,也是实验室中的一个有问题的污染物。非细胞病变性 BVDV 感染可能未被注意到,并通过存在于用于细胞培养的污染牛血清中感染实验室细胞系。BVDV 被认为是一种有价值的替代病毒模型,可用于鉴定和表征用于治疗 HCV 的抗病毒药物。在病毒复制的某些方面,BVDV 比目前使用的 HCV 复制子系统更有利。在这篇综述中,我们报告了迄今为止测定的一系列化合物的设计、合成和对 BVDV 的活性。