Discovery of FDA-Approved Drugs as Inhibitors of Fatty Acid Binding Protein 4 Using Molecular Docking Screening

被引:36
|
作者
Wang, Yan [1 ]
Law, Wai-Kit [1 ]
Hu, Jian-Shu [1 ]
Lin, Huang-Quan [2 ,3 ]
Ip, Tsz-Ming [1 ]
Wan, David Chi-Cheong [1 ]
机构
[1] Chinese Univ Hong Kong, Fac Med, Sch Biomed Sci, Shatin, Hong Kong, Peoples R China
[2] Hong Kong Univ Sci & Technol, Div Life Sci, Hong Kong, Hong Kong, Peoples R China
[3] Hong Kong Univ Sci & Technol, Ctr Chinese Med, Hong Kong, Hong Kong, Peoples R China
关键词
PPAR-GAMMA; LEVOFLOXACIN; HYPOGLYCEMIA; ATHEROSCLEROSIS; METABOLISM; EFFICACY; TARGETS; OBESITY; FUTURE;
D O I
10.1021/ci500503b
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
We first identified fluorescein, ketazolam, antrafenine, darifenacin, fosaprepitant, paliperidone, risperidone, pimozide, trovafloxacin, and levofloxacin as inhibitors of fatty acid binding protein 4 using molecular docking screening from FDA-approved drugs. Subsequently, the biochemical characterizations showed that levofloxacin directly inhibited FABP4 activity in both the in vitro ligand displacement assay and cell-based function assay. Furthermore, levofloxacin did not induce adipogenesis in adipocytes, which is the major adverse effect of FABP4 inhibitors.
引用
收藏
页码:3046 / 3050
页数:5
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