Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Hengxian Cui"'
Autor:
Wenbo Yin, Tianxiao Wu, Lei Liu, Hong Jiang, Yuxin Zhang, Hengxian Cui, Yin Sun, Qiaohua Qin, Yixiang Sun, Zixuan Gao, Liyu Zhao, Xin Su, Dongmei Zhao, Maosheng Cheng
Publikováno v:
Journal of medicinal chemistry. 65(7)
Invasive fungal infections are emerging as serious infectious diseases worldwide. Because of the development of antifungal drug resistance, the limited efficacy of the existing drugs has led to high mortality in patients. The use of the essential euk
Autor:
Wenbo Yin, Lei Liu, Hong Jiang, Tianxiao Wu, Hengxian Cui, Yuxin Zhang, Zixuan Gao, Yin Sun, Qiaohua Qin, Liyu Zhao, Xin Su, Dongmei Zhao, Maosheng Cheng
Publikováno v:
European journal of medicinal chemistry. 233
Invasive fungal infections (IFIs) are emerging as serious infectious diseases worldwide, and due to the lack of effective antifungal agents and serious drug resistance, the limited efficacy of existing drugs has led to high morbidity and mortality in
Autor:
Dongmei Zhao, Lei Liu, Tianxiao Wu, Hengxian Cui, Hong Jiang, Yuxin Zhang, Maosheng Cheng, Yang Zheng, Yin Sun, Xin Su, Song Li, Liyu Zhao, Wenbo Yin
Publikováno v:
European journal of medicinal chemistry. 225
A series of 5-phenylthiophene derivatives with novel structures were designed and synthesized to combat the increasing incidence of susceptible and drug-resistant fungal infections. The antifungal activity of the synthesized compounds was assessed ag
Autor:
Dongmei Zhao, Liyu Zhao, Wenbo Yin, Hengxian Cui, Xin Su, Hong Jiang, Tianxiao Wu, Lei Liu, Maosheng Cheng, Yin Sun, Yuxin Zhang
Publikováno v:
European Journal of Medicinal Chemistry. 227:113955
5-phenylthiophene derivatives exhibited excellent antifungal activity against Candida albicans, Candida tropicalis and Cryptococcus neoformans. However, optimal compound 7 was inactive against Aspergillus fumigatus and unstable in human liver microso
Autor:
Dongmei Zhao, Ruifeng Wang, Xiangxin Zhao, Maosheng Cheng, Hengxian Cui, Chenzhou Hao, Tianxiao Wu, Yixuan Chen, Sijia Yu
Publikováno v:
Bioorganic Chemistry. 102:104092
Focal adhesion kinase (FAK) is an intracellular non-receptor tyrosine kinase responsible for development of various tumor types. Aiming to explore new potent inhibitors, two series of 2,4-disubstituted-7H-pyrrolo[2,3-d]pyrimidine derivatives were des