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公开(公告)号:US20220370416A1
公开(公告)日:2022-11-24
申请号:US17223551
申请日:2021-04-06
Applicant: Arvinas Operations, Inc. , Yale University
Inventor: Ling Chu , Craig M. Crews , Hanqing Dong , Keith R. Hornberger , Jesus Raul Medina , Lawrence Snyder , Jing Wang
IPC: A61K31/427 , A61K47/54 , A61K45/06 , A61K31/422 , A61K31/4155
Abstract: Bifunctional compounds, which find utility as modulators of Kirsten ras sarcoma protein (KRas or KRAS), are described herein. In particular, the hetero-bifunctional compounds of the present disclosure contain on one end a moiety that binds to the Von Hippel-Lindau E3 ubiquitin ligase and on the other end a moiety which binds KRas, such that the target protein is placed in proximity to the ubiquitin ligase to effect degradation (and inhibition) of target protein. The hetero-bifunctional compounds of the present disclosure exhibit a broad range of pharmacological activities associated with degradation/inhibition of target protein. Diseases or disorders that result from aberrant regulation of the target protein are treated or prevented with compounds and compositions of the present disclosure.
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公开(公告)号:US10994015B2
公开(公告)日:2021-05-04
申请号:US15852854
申请日:2017-12-22
Applicant: Arvinas Operations, Inc. , Yale University
Inventor: Andrew P. Crew , Kurt Zimmermann , Jing Wang , Craig M. Crews , Saul Jaime-Figueroa , George Burslem
IPC: C07D471/04 , A61P35/00 , A61K31/506 , A61K47/54 , A61K47/55 , A61K31/519 , A61K31/427 , A61K31/454 , A61K31/517 , A61K31/55 , A61K31/496 , A61K31/551 , A61K45/06 , A61K38/07 , A61K31/52
Abstract: The present disclosure relates to bifunctional compounds, which find utility as modulators of receptor tyrosine kinase (RTK) proteins. In particular, the present disclosure is directed to bifunctional compounds, which contain on one end a ligand which binds to an E3 ubiquitin ligase and on the other end a moiety which binds a target protein, such that the target protein is placed in proximity to the ubiquitin ligase to effectuate ubiquitination, and therefore, degradation (and inhibition) of the target protein. The present disclosure exhibits a broad range of pharmacological activities associated with degradation/inhibition of target protein. Diseases or disorders that result from aggregation or accumulation of the target protein are treated or prevented with compounds and compositions of the present disclosure.
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公开(公告)号:US20240382599A1
公开(公告)日:2024-11-21
申请号:US18623722
申请日:2024-04-01
Applicant: Arvinas Operations, Inc. , Yale University
Inventor: Andrew P. Crew , Kurt Zimmermann , Jing Wang , Michael Berlin , Hanqing Dong , Alexey Ishchenko , Yimin Qian , Saul Jaime-Figueroa , George Burslem , Craig M. Crews
IPC: A61K47/54 , A61K31/427 , A61K31/454 , A61K31/496 , A61K31/506 , A61K31/517 , A61K31/519 , A61K31/52 , A61K31/55 , A61K31/551 , A61K38/07 , A61K45/06 , A61K47/55 , C07D471/04
Abstract: The present invention relates to bifunctional compounds, which find utility to degrade and (inhibit) TBK1. In particular, the present invention is directed to compounds, which contain on one end an E3 ubiquitin ligase binding moiety which binds to an E3 ubiquitin ligase and on the other end a moiety which binds TBK1 such that TBK1 is placed in proximity to the ubiquitin ligase to effect degradation (and inhibition) of TBK1. The present invention exhibits a broad range of pharmacological activities associated with compounds according to the present invention, consistent with the degradation/inhibition of TBK1.
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14.
公开(公告)号:US11173211B2
公开(公告)日:2021-11-16
申请号:US16563842
申请日:2019-09-07
Applicant: ARVINAS OPERATIONS, INC. , YALE UNIVERSITY
Inventor: Andrew P. Crew , Keith R. Hornberger , Jing Wang , Saul Jaime-Figueroa , Hanqing Dong
IPC: C07D401/14 , C07D471/04 , A61K31/437 , A61P35/00 , A61K47/55 , C07D519/00 , C07D417/14 , C07D413/14
Abstract: The present disclosure relates to bifunctional compounds, which find utility as modulators of Rapidly Accelerated Fibrosarcoma (RAF, such as c-RAF, A-RAF and/or B-RAF; the target protein). In particular, the present disclosure is directed to bifunctional compounds, which contain on one end a Von Hippel-Lindau, cereblon, Inhibitors of Apotosis Proteins or mouse double-minute homolog 2 ligand which binds to the respective E3 ubiquitin ligase and on the other end a moiety which binds the target protein RAF, such that the target protein is placed in proximity to the ubiquitin ligase to effect degradation (and inhibition) of target protein. The present disclosure exhibits a broad range of pharmacological activities associated with degradation/inhibition of target protein. Diseases or disorders that result from aggregation or accumulation of the target protein, or the constitutive activation of the target protein, are treated or prevented with compounds and compositions of the present disclosure.
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公开(公告)号:US12239711B2
公开(公告)日:2025-03-04
申请号:US17571018
申请日:2022-01-07
Applicant: Arvinas Operations, Inc.
Inventor: Andrew P. Crew , Craig M. Crews , Hanqing Dong , Keith R. Hornberger , Yimin Qian , Lawrence B. Snyder , Jing Wang
IPC: C07D401/04 , A61K31/437 , A61K31/496 , A61K31/497 , A61K31/501 , A61K31/506 , A61K31/551 , A61K45/06 , A61K47/54 , A61K47/55 , A61P35/00 , C07D401/14 , C07D471/04
Abstract: The description relates to cereblon E3 ligase binding compounds, including bifunctional compounds comprising the same, which find utility as modulators of targeted ubiquitination, especially inhibitors of a variety of polypeptides and other proteins which are degraded and/or otherwise inhibited by bifunctional compounds according to the present disclosure. In particular, the description provides compounds, which contain on one end a ligand which binds to the cereblon E3 ubiquitin ligase and on the other end a moiety which binds a target protein such that the target protein is placed in proximity to the ubiquitin ligase to effect degradation (and inhibition) of that protein. Compounds can be synthesized that exhibit a broad range of pharmacological activities consistent with the degradation/inhibition of targeted polypeptides of nearly any type.
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公开(公告)号:US12180193B2
公开(公告)日:2024-12-31
申请号:US17459179
申请日:2021-08-27
Applicant: Arvinas Operations, Inc.
Inventor: Keith R. Hornberger , Jing Wang
IPC: C07D403/14
Abstract: Bifunctional compounds, which find utility as modulators of Rapidly Accelerated Fibrosarcoma (Raf, such as c-Raf, A-Raf, and/or B-Raf), are described herein. In particular, the hetero-bifunctional compounds of the present disclosure contain on one end a moiety that binds to the cereblon E3 ubiquitin ligase and on the other end a moiety which binds Raf, such that the target protein is placed in proximity to the ubiquitin ligase to effect degradation (and inhibition) of target protein. The hetero-bifunctional compounds of the present disclosure exhibit a broad range of pharmacological activities associated with degradation/inhibition of target protein. Diseases or disorders that result from aberrant regulation of the target protein are treated or prevented with compounds and compositions of the present disclosure.
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17.
公开(公告)号:US12172981B2
公开(公告)日:2024-12-24
申请号:US17359424
申请日:2021-06-25
Applicant: Arvinas Operations, Inc.
Inventor: Andrew P. Crew , Hanqing Dong , Keith R. Hornberger , Yimin Qian , Jing Wang
IPC: C07D401/14 , A61K31/454 , A61K31/4545 , A61K31/4725 , A61K31/496 , A61K31/497 , A61K31/501 , A61K31/519 , A61K31/5386 , A61K31/551 , A61K38/05 , A61K38/06 , A61K45/06 , A61K47/54 , A61P15/00 , A61P35/00 , C07D401/04 , C07D471/04 , C07D471/10 , C07D487/04 , C07D487/08 , C07D487/10 , C07D498/10 , C07K5/078 , C07K5/083 , C07K5/062
Abstract: The present disclosure relates to bifunctional compounds, which find utility as modulators of estrogen receptor (target protein). In particular, the present disclosure is directed to bifunctional compounds, which contain on one end at least one of a Von Hippel-Lindau ligand, a cereblon ligand, Inhibitors of Apoptosis Proteins ligand, mouse double-minute homolog 2 ligand, or a combination thereof, which binds to the respective E3 ubiquitin ligase, and on the other end a moiety which binds the target protein, such that the target protein is placed in proximity to the ubiquitin ligase to effect degradation (and inhibition) of target protein. The present disclosure exhibits a broad range of pharmacological activities associated with degradation/inhibition of target protein. Diseases or disorders that result from aggregation or accumulation of the target protein are treated or prevented with compounds and compositions of the present disclosure.
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公开(公告)号:US11384063B2
公开(公告)日:2022-07-12
申请号:US16810764
申请日:2020-03-05
Applicant: Arvinas Operations, Inc.
Inventor: Andrew P. Crew , Hanqing Dong , Jing Wang , Yimin Qian
IPC: C07D401/14 , C07D471/04 , C07D409/12 , C07D403/06 , A61P35/00 , C07D405/14 , C07D413/14 , C07D417/12 , C07D417/14 , C07D403/14
Abstract: The present disclosure relates to bifunctional compounds, which find utility as modulators of estrogen receptor (target protein). In particular, the present disclosure is directed to bifunctional compounds, which contain on one end a cereblon, Von Hippel-Lindau ligase-binding moiety, Inhibitors of Apotosis Proteins, or mouse double-minute homolog 2 ligand, which binds to the respective E3 ubiquitin ligase, and on the other end a moiety which binds the target protein, such that the target protein is placed in proximity to the ubiquitin ligase to effect degradation (and inhibition) of target protein. The present disclosure exhibits a broad range of pharmacological activities associated with degradation/inhibition of target protein. Diseases or disorders that result from aggregation or accumulation of the target protein are treated or prevented with compounds and compositions of the present disclosure.
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19.
公开(公告)号:US20220144809A1
公开(公告)日:2022-05-12
申请号:US17512219
申请日:2021-10-27
Applicant: Arvinas Operations, Inc.
Inventor: Hanqing Dong , Lawrence B. Snyder , Jing Wang
IPC: C07D401/14 , A61K45/06
Abstract: Bifunctional compounds, which find utility as modulators of androgen receptor (AR), are described herein. In particular, the bifunctional compounds of the present disclosure contain on one end a moiety that binds to the cereblon E3 ubiquitin ligase and on the other end a moiety which binds AR, such that the target protein is placed in proximity to the ubiquitin ligase to effect degradation (and inhibition) of target protein. The bifunctional compounds of the present disclosure exhibit a broad range of pharmacological activities associated with degradation/inhibition of target protein. Diseases or disorders that result from aberrant regulation of the target protein are treated or prevented with compounds and compositions of the present disclosure.
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公开(公告)号:US20220127279A1
公开(公告)日:2022-04-28
申请号:US17570197
申请日:2022-01-06
Applicant: Arvinas Operations, Inc.
Inventor: Andrew P. Crew , Craig M. Crews , Hanqing Dong , Yimin Qian , Jing Wang
IPC: C07D495/14 , A61K45/06 , C07D417/12 , C07D401/14 , C07D207/16 , C07D401/12 , C07D405/14 , A61K31/506 , A61K47/55 , A61K31/436 , A61K31/337 , A61K31/4995 , A61K31/593 , A61K31/4545 , A61K31/4184 , A61K31/704 , A61K31/664
Abstract: The description relates to MDM2 binding compounds, including bifunctional compounds comprising the same, which find utility as modulators of targeted ubiquitination, especially inhibitors of a variety of polypeptides and other proteins which are degraded and/or otherwise inhibited by bifunctional compounds according to the present invention. In particular, the description provides compounds, which contain on one end a ligand which binds to the MDM2 E3 ubiquitin ligase and on the other end a moiety which binds a target protein such that the target protein is placed in proximity to the ubiquitin ligase to effect degradation (and inhibition) of that protein. Compounds can be synthesized that exhibit a broad range of pharmacological activities consistent with the degradation/inhibition of targeted polypeptides of nearly any type.
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