Zhang Jie, Xu Wenfang
Department of Medicinal Chemistry, School of Pharmaceutical Sciences, ShanDong University, 44, West Culture Road, 250012, Ji'nan, ShanDong, P.R. China.
Mini Rev Med Chem. 2006 Apr;6(4):429-48. doi: 10.2174/138955706776361475.
Neuraminidase (NA) is the major surface glycoprotein of the influenza virus. It has been considered a suitable target for designing agents against influenza viruses. Rational drug design of NA inhibitors is now in the clinic and is effective for the treatment of influenza. Recently, research of structure-based NA inhibitors is becoming an interesting field, leading to a breakthrough in the control of influenza. Here we review a series of neuraminidase inhibitors and the recent progress in this field.
神经氨酸酶(NA)是流感病毒的主要表面糖蛋白。它一直被认为是设计抗流感病毒药物的合适靶点。目前,NA抑制剂的合理药物设计已进入临床阶段,对流感治疗有效。最近,基于结构的NA抑制剂研究正成为一个有趣的领域,并在流感防控方面取得了突破。在此,我们综述了一系列神经氨酸酶抑制剂以及该领域的最新进展。