组蛋白脱乙酰基酶
白色念珠菌
髓系白血病
白血病
氟康唑
癌症研究
化学
药理学
医学
免疫学
生物
组蛋白
微生物学
抗真菌
生物化学
基因
作者
Yahui Huang,Guoqiang Dong,Huanqiu Li,Na Liu,Wannian Zhang,Chunquan Sheng
标识
DOI:10.1021/acs.jmedchem.8b00393
摘要
Clinically, leukemia patients often suffer from the limited efficacy of chemotherapy and high risks of infection by invasive fungal pathogens. Herein, a novel therapeutic strategy was developed in which a small molecule can simultaneously treat leukemia and invasive fungal infections (IFIs). Novel Janus kinase 2 (JAK2) and histone deacetylase (HDAC) dual inhibitors were identified to possess potent anti-proliferative activity toward hematological cell lines and excellent synergistic effects with fluconazole to treat resistant Candida albicans infections. In particular, compound 20a, a highly active and selective JAK2/HDAC6 dual inhibitor, showed excellent in vivo antitumor efficacy in several acute myeloid leukemia (AML) models and synergized with fluconazole for the treatment of resistant C. albicans infections. This study highlights the therapeutic potential of JAK2/HDAC dual inhibitors in treating AML and IFIs and provides an efficient strategy for multitargeting drug discovery.
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