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公开(公告)号:US20230037322A1
公开(公告)日:2023-02-09
申请号:US17849949
申请日:2022-06-27
发明人: Rebecca Grange , John Allingham , Andrew Craig , P. Andrew Evans , Madhu Aeluri
IPC分类号: A61K31/45 , A61K31/221 , A61K31/25 , A61K31/341 , A61K31/397 , A61K31/4015 , A61K45/06 , A61K47/36 , C07C235/28 , C07C321/10 , C07D205/08 , C07D207/27 , C07D211/76 , C07D307/46
摘要: A class of compounds useful in pharmaceutical compositions and methods for treating or preventing cancer is described. Analogs of Mycalolide B have been prepared and tested in breast and ovarian cancer cell lines. The compounds show utility for inhibition of survival and proliferation of tumor cells. The compounds have been shown to disrupt actin.
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公开(公告)号:US11369594B2
公开(公告)日:2022-06-28
申请号:US16639207
申请日:2018-08-17
发明人: Rebecca Grange , John Allingham , Andrew Craig , P. Andrew Evans , Madhu Aeluri
IPC分类号: A61K31/45 , A61K45/06 , A61K47/36 , A61K31/221 , A61K31/25 , A61K31/341 , A61K31/4015 , A61K31/397 , C07D211/76 , C07D207/27 , C07D205/08 , C07D307/46 , C07D321/10 , C07C235/28 , C07C321/10
摘要: A class of compounds useful in pharmaceutical compositions and methods for treating or preventing cancer is described. Analogs of Mycalolide B have been prepared and tested in breast and ovarian cancer cell lines. The compounds show utility for inhibition of survival and proliferation of tumor cells. The compounds have been shown to disrupt actin.
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公开(公告)号:US20200306233A1
公开(公告)日:2020-10-01
申请号:US16639207
申请日:2018-08-17
发明人: Rebecca Grange , John Allingham , Andrew Craig , P. Andrew Evans , Madhu Aeluri
IPC分类号: A61K31/45 , A61K45/06 , A61K47/36 , A61K31/221 , A61K31/25 , A61K31/341 , A61K31/4015 , A61K31/397 , C07D211/76 , C07D207/27 , C07D205/08 , C07D307/46 , C07C321/10 , C07C235/28
摘要: A class of compounds useful in pharmaceutical compositions and methods for treating or preventing cancer is described. Analogs of Mycalolide B have been prepared and tested in breast and ovarian cancer cell lines. The compounds show utility for inhibition of survival and proliferation of tumor cells. The compounds have been shown to disrupt actin.
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