Quinazolinone Compounds Have Potent Antiviral Activity against Zika and Dengue Virus

被引:9
|
作者
Ashraf-Uz-Zaman, Md [1 ]
Li, Xin [1 ]
Yao, Yuan [1 ]
Mishra, Chandra Bhushan [1 ]
Moku, Bala Krishna [1 ]
Song, Yongcheng [1 ,2 ]
机构
[1] Baylor Coll Med, Dept Pharmacol & Chem Biol, Houston, TX 77030 USA
[2] Baylor Coll Med, Dan L Duncan Comprehens Canc Ctr, Houston, TX 77030 USA
基金
美国国家卫生研究院;
关键词
ALLOSTERIC INHIBITORS; INFECTION;
D O I
10.1021/acs.jmedchem.3c00924
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Dengue (DENV) and Zika (ZIKV) viruses are important human pathogens, causing similar to 100 million symptomatic infections each year. These infections carry a 20-fold increased incidence of serious neurological diseases, such as microcephaly in newborns (for ZIKV) and Guillain-Barre ' syndrome. Moreover, DENV can develop serious and possibly life-threatening dengue hemorrhagic fever in certain patients. Patients recovered from one of the four serotypes of DENV are still susceptible to other serotypes with a higher likelihood of serious disease because of antibody-dependent enhancement. Except for mosquito control, there have been no antiviral drugs to prevent and treat ZIKV/ DENV infections. Phenotypic screening found that 2,3,6-trisubstituted quinazolinone compounds are novel inhibitors of ZIKV replication. Fiftyfour analogues were synthesized, and their structure-activity relationships are discussed. Additional testing shows that compounds 22, 27, and 47 exhibited broad and potent activities against ZIKV and DENV with EC50 values as low as 86 nM with no significant cytotoxicity to mammalian cells.
引用
收藏
页码:10746 / 10760
页数:15
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