喹诺酮类
埃替拉韦
人类免疫缺陷病毒(HIV)
药品
大流行
体内
药理学
医学
病毒学
化学
生物
2019年冠状病毒病(COVID-19)
抗逆转录病毒疗法
抗生素
传染病(医学专业)
内科学
生物技术
生物化学
病毒载量
疾病
作者
Ruo Wang,Kai Xu,Weixiong Shi
标识
DOI:10.1002/ardp.201900045
摘要
Abstract Acquired immune deficiency syndrome (AIDS)/human immunodeficiency virus (HIV) is one of the largest and most devastating public health pandemics throughout the world. The global pandemic of drug‐sensitive HIV and the increasing threat from drug‐resistant HIV result in an urgent need to develop more effective anti‐HIV candidates. Quinolone represents a significant class of privileged heterocycles, and its derivatives possess promising in vitro and in vivo anti‐HIV properties. The 4‐quinolone elvitegravir has already been approved for the treatment of HIV; thus, quinolone derivatives might be promising candidates with anti‐HIV activity. This review emphasizes quinolone derivatives with potential anti‐HIV activity, covering articles published between 1992 and 2019. The structure‐activity relationship is also discussed to provide insights for further development of more active quinolone derivatives.
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