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1.
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:EP3724216A1
公开(公告)日:2020-10-21
申请号:EP18839646.9
申请日:2018-12-14
发明人: MOURTADA, Rida , HERCE, Henry D. , WALENSKY, Loren D. , BIRD, Gregory H. , MORGAN, Ann Maurine , BRADNER, James E.
IPC分类号: C07K14/435
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3.
公开(公告)号:EP3737404A1
公开(公告)日:2020-11-18
申请号:EP18842760.3
申请日:2018-12-13
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公开(公告)号:EP2858661B1
公开(公告)日:2020-04-22
申请号:EP12861273.6
申请日:2012-12-31
IPC分类号: A61K47/60 , A61K39/12 , A61K38/00 , C07K14/005 , C12N7/00
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公开(公告)号:EP3270945A2
公开(公告)日:2018-01-24
申请号:EP16765822.8
申请日:2016-03-18
CPC分类号: C07K14/4702 , A61K38/00 , A61K38/16
摘要: Provided herein are stabilized peptides that bind Mcl-1. 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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6.
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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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8.
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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10.
公开(公告)号:EP3360892A1
公开(公告)日:2018-08-15
申请号:EP18164082.2
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 β-catenin in vitro, in cellulo, and in vivo, disrupting the BCL-9/β-catenin interaction, and thereby interfering with deregulated Wnt/β-catenin signaling for therapeutic benefit in a variety of human diseases including human cancer.
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