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公开(公告)号:US11111253B2
公开(公告)日:2021-09-07
申请号:US16846089
申请日:2020-04-10
发明人: Donna M. Huryn , Peter Wipf , Jennifer Rubin Grandis , Matthew G. LaPorte , Paul A. Johnston , Mark E. Schurdak , Raffaele Colombo
IPC分类号: C07D513/04 , A61P35/00
摘要: Compounds that selectivity inhibit the STAT3 pathway and not the STAT1 pathway and exhibit anti-proliferative activity are disclosed. Also disclosed are methods of treatment of cancers that are characterized by overexpression of STAT3, which are safer that other therapies.
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公开(公告)号:US20200339602A1
公开(公告)日:2020-10-29
申请号:US16846089
申请日:2020-04-10
发明人: Donna M. Huryn , Peter Wipf , Jennifer Rubin Grandis , Matthew G. LaPorte , Paul A. Johnston , Mark E. Schurdak , Raffaele Colombo
IPC分类号: C07D513/04 , A61P35/00
摘要: Compounds that selectivity inhibit the STAT3 pathway and not the STAT1 pathway and exhibit anti-proliferative activity are disclosed. Also disclosed are methods of treatment of cancers that are characterized by overexpression of STAT3, which are safer that other therapies.
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公开(公告)号:US20200216410A1
公开(公告)日:2020-07-09
申请号:US16612342
申请日:2018-05-10
发明人: Donna M. Huryn , Peter Wipf , Matthew G. LaPorte
IPC分类号: C07D401/04 , C07D401/14
摘要: The present technology is directed to methods of inhibiting or modulating p97 and compounds and compositions useful in such methods Diseases and conditions that can be treated with the compounds and compositions of the present technology include, but are not limited to, antibacterial infection, antiviral infection, cancer and neurodegenerative disorders susceptible to treatment by inhibition or modulation of p97.
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公开(公告)号:US20190100535A1
公开(公告)日:2019-04-04
申请号:US15543573
申请日:2016-01-15
发明人: Donna M. Huryn , Peter Wipf , Jennifer Rubin Grandis , Matthew G. LaPorte , Paul A. Johnston , Mark E. Schurdak , Raffaele Colombo
IPC分类号: C07D513/04 , A61P35/00
摘要: Compounds that selectivity inhibit the STAT3 pathway and not the STAT1 pathway and exhibit anti-proliferative activity are disclosed. Also disclosed are methods of treatment of cancers that are characterized by overexpression of STAT3, which are safer that other therapies.
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