Department of Pharmacology, Yale University School of Medicine, 333 Cedar Street, New Haven, CT 06520, USA.
Antimicrob Agents Chemother. 2010 Jan;54(1):197-206. doi: 10.1128/AAC.01206-09. Epub 2009 Nov 9.
Recent years have seen the rapid advancement of new therapeutic agents against hepatitis C virus (HCV) in response to the need for treatment that is unmet by interferon (IFN)-based therapies. Most antiviral drugs discovered to date are small molecules that modulate viral enzyme activities. In the search for highly selective protein-binding molecules capable of disrupting the viral life cycle, we have identified a class of anionic tetraphenylporphyrins as potent and specific inhibitors of the HCV replicons. Based on the structure-activity relationship studies reported herein, meso-tetrakis-(3,5-dicarboxy-4,4'-biphenyl) porphyrin was found to be the most potent inhibitor of HCV genotype 1b (Con1) replicon systems but was less effective against the genotype 2a (JFH-1) replicon. This compound induced a reduction of viral RNA and protein levels when acting in the low nanomolar range. Moreover, the compound could suppress replicon rebound in drug-treated cells and exhibited additive to synergistic effects when combined with protease inhibitor BILN 2061 or with IFN-alpha-2a. Our results demonstrate the potential use of tetracarboxyphenylporphyrins as potent anti-HCV agents.
近年来,针对干扰素(IFN)为基础的治疗方法无法满足的治疗需求,出现了许多针对丙型肝炎病毒(HCV)的新型治疗药物。迄今为止发现的大多数抗病毒药物都是小分子,可调节病毒酶的活性。为了寻找能够破坏病毒生命周期的高选择性蛋白结合分子,我们发现了一类阴离子四苯基卟啉类化合物,它们是 HCV 复制子的有效且特异性抑制剂。基于本文报道的构效关系研究,发现间四-(3,5-二羧基-4,4'-联苯)卟啉对 HCV 基因型 1b (Con1) 复制子系统的抑制作用最强,但对基因型 2a (JFH-1) 复制子的作用较弱。该化合物在低纳摩尔范围内作用时,可降低病毒 RNA 和蛋白水平。此外,该化合物可抑制药物处理细胞中的复制子反弹,并与蛋白酶抑制剂 BILN 2061 或 IFN-α-2a 联合使用时具有相加至协同作用。我们的研究结果表明,四羧基苯基卟啉类化合物具有作为有效抗 HCV 药物的潜力。