发明申请
US20100168417A1 2-Indolyl Imidazo [4,5-d] Phenanthroline Derivatives and Their Use in the Treatment for Cancer
有权
2-吲哚咪唑并[4,5-d]菲咯啉衍生物及其在癌症治疗中的应用
- 专利标题: 2-Indolyl Imidazo [4,5-d] Phenanthroline Derivatives and Their Use in the Treatment for Cancer
- 专利标题(中): 2-吲哚咪唑并[4,5-d]菲咯啉衍生物及其在癌症治疗中的应用
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申请号: US11915257申请日: 2006-05-25
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公开(公告)号: US20100168417A1公开(公告)日: 2010-07-01
- 发明人: Mario Huesca , Aiping H. Young , Yoon Lee , Aye Aye Khine , Jim A. Wright , Lisa Lock , Raed Al-Qawasmeh
- 申请人: Mario Huesca , Aiping H. Young , Yoon Lee , Aye Aye Khine , Jim A. Wright , Lisa Lock , Raed Al-Qawasmeh
- 国际申请: PCT/IB2006/051675 WO 20060525
- 主分类号: C07D401/14
- IPC分类号: C07D401/14 ; C07D471/16 ; C07D413/14
摘要:
2-indolyl imidazo[4,5-d]phenanthroline compounds of Formula I that are capable of intracellular chelation of transition metals and of exerting antiproliferative effects in cancer cells, that are cytostatic and/or cytotoxic, are provided. Compounds of Formula I can also induce apoptosis in cancer cells and are thus capable of exerting a cytotoxic effect on cancer cells. The compounds of Formula I are also capable of selectively inhibiting the proliferation of one or more of prostate cancer cells, colon cancer cells, non-small lung cancer cells and leukemia cells. The compounds of Formula I are also capable of increasing the expression of the zinc-regulated tumour suppressor, KLF4 and thus are useful in inhibiting the proliferation of cancer cells in which KLF4 functions as a tumour-suppressor, including, but not limited to, bladder cancer, cancers of the gastrointestinal tract and various leukemias.
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