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1.
公开(公告)号:EP3503924A2
公开(公告)日:2019-07-03
申请号:EP17771914.3
申请日:2017-08-25
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2.
公开(公告)号:EP2118123B1
公开(公告)日:2015-10-14
申请号:EP08728649.8
申请日:2008-01-31
CPC分类号: C07K14/4746 , A61K38/00 , C07K1/113
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公开(公告)号:EP2118123A1
公开(公告)日:2009-11-18
申请号:EP08728649.8
申请日:2008-01-31
IPC分类号: C07K7/54
CPC分类号: C07K14/4746 , A61K38/00 , C07K1/113
摘要: Cross-linked peptides related to human p53 and bind to HMD2 or a family member of HDM2 useful for promoting apoptosis, e.g., in the treatment of and identifying therapeutic agents that binding to HMD2 or a family member of HDM2.
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4.
公开(公告)号:EP4399220A1
公开(公告)日:2024-07-17
申请号:EP22785887.5
申请日:2022-09-08
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公开(公告)号:EP2970418A2
公开(公告)日:2016-01-20
申请号:EP14767620.9
申请日:2014-03-13
发明人: WALENSKY, Loren D.
CPC分类号: C12N9/96 , A61K38/00 , C07K14/47 , C12N9/1007 , C12Y201/01043
摘要: Provided herein are polypeptides containing stabilized therapeutic peptides related to enhancer of zeste homolog 2 (EZH2), histone lysine N-methyltransferase. Also provided are compositions containing these polypeptides and methods of using such peptides in the treatment of cancer that include administering to a subject one of the polypeptides.
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公开(公告)号:EP2766355A2
公开(公告)日:2014-08-20
申请号:EP12840731.9
申请日:2012-10-11
发明人: WALENSKY, Loren D.
IPC分类号: C07D403/04 , C07D417/04 , A61K31/415 , A61P35/00
CPC分类号: C07D417/04 , A61K31/4155 , A61K31/4178 , A61K31/427 , A61K31/497 , C07D403/04 , C07D403/14 , C07D413/04 , C07D417/14
摘要: This application features pyrazol-3-one compounds that activate pro-apoptotic BAX. Also featured are methods of using such compounds, e.g., for the treatment or prevention of diseases, disorders, and conditions associated with deregulated apoptosis of cells (e.g., insufficient apoptosis of diseased or damaged cells or essentially the absence of apoptosis of diseased or damaged cells).
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7.
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公开(公告)号:EP3715366A1
公开(公告)日:2020-09-30
申请号:EP20172306.1
申请日:2012-04-16
摘要: The invention provides structurally-constrained peptides by hydrocarbon stapling of a BCL9 HD2 helix for use as a therapeutic agent. The invention further provides methods and kits for use of the structurally-constrained peptide of the instant invention. The invention is based, at least in part, on the results provided herein demonstrating that hydrocarbon stapled helical peptides display excellent proteolytic, acid, and thermal stability, restore the native helical structure of the peptide, possess superior pharmacokinetic properties compared to the corresponding unmodified peptides, and are highly effective in binding to ß-catenin in vitro, in cellulo, and in vivo, disrupting the BCL-9/ß-catenin interaction, and thereby interfering with deregulated Wnt/ß-catenin signaling for therapeutic benefit in a variety of human diseases including human cancer.
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公开(公告)号:EP4228699A1
公开(公告)日:2023-08-23
申请号:EP21811174.8
申请日:2021-10-14
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