Expanding the structural diversity of Bcr-Abl inhibitors: Dibenzoylpiperazin incorporated with 1H-indazol-3-amine.
Expanding the structural diversity of Bcr-Abl inhibitors: Dibenzoylpiperazin incorporated with 1H-indazol-3-amine.
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扩大 Bcr-Abl 抑制剂的结构多样性:二苯甲酰哌嗪与 1H-吲唑-3-胺结合。
DOI:
10.1016/j.ejmech.2015.09.034
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发表时间:
2015-11
影响因子:
6.7
通讯作者:
Wang Maoyi
中科院分区:
文献类型:
--
作者:
Shan Yuanyuan;Dong Jinyun;Pan Xiaoyan;Zhang Lin;Zhang Jie;Dong Yalin;Wang Maoyi
A series ofN,N'-dibenzoylpiperazine derivatives incorporated with 1H-indazol-3-amine have been designed, synthesized and evaluated as novel Bcr-Abl inhibitors. Several title compounds exhibited potent inhibitory activity against Bcr-Abl wild type as well as T315I mutant. Two compounds,11aand12c, strongly suppressed the activity of native and mutant Bcr-Abl. In particular,11aexhibited comparable potency with that of Imatinib. It potently inhibited both Bcr-AblWTand Bcr-AblT315Iwith IC50values of 0.014 μM and 0.45 μM, respectively. Furthermore, compound11aalso inhibited the proliferation of K562 leukemia cancer cells. Therefore, it could serve as promising lead compound for further optimization of Bcr-AblWTand Bcr-AblT315Iinhibitors.
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DOI:
10.1039/c3md00192j
发表时间:
2013-10
期刊:
Medicine Chemical Communications
影响因子:
--
作者:
Wang Cheng;Dong Jinyun;Zhang Yanmin;Wang Fang;Gao Hongping;Li Pengfei;Wang Sicen;Zhang Jie
通讯作者:
Zhang Jie
DOI:
10.1016/j.critrevonc.2011.04.002
发表时间:
2012-05
期刊:
Critical reviews in oncology/hematology
影响因子:
--
作者:
G. Rosti;F. Castagnetti;G. Gugliotta;F. Palandri;M. Baccarani
通讯作者:
G. Rosti;F. Castagnetti;G. Gugliotta;F. Palandri;M. Baccarani
影响因子:
6.7
作者:
H. M. Revankar;M. Kulkarni;S. Joshi;U. A. More
通讯作者:
H. M. Revankar;M. Kulkarni;S. Joshi;U. A. More
影响因子:
7.3
作者:
Radi, Marco;Tintori, Cristina;Botta, Maurizio
通讯作者:
Botta, Maurizio
影响因子:
4.6
作者:
Shengqian Ma;Daofeng Sun;P. Forster;Daqiang Yuan;Wenjuan Zhuang;Yu‐Sheng Chen;J. Parise;Hongcai Zhou
通讯作者:
Shengqian Ma;Daofeng Sun;P. Forster;Daqiang Yuan;Wenjuan Zhuang;Yu‐Sheng Chen;J. Parise;Hongcai Zhou