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公开(公告)号:US20210187108A1
公开(公告)日:2021-06-24
申请号:US16912329
申请日:2020-06-25
Applicant: Arvinas Operations, Inc. , Yale University
Inventor: Yimin Qian , Hanqing Dong , Jing Wang , Michael Berlin , Andrew P. Crew , Craig M. Crews
IPC: A61K45/06 , C07D519/00 , C07D417/14 , C07D495/14 , A61K47/55
Abstract: The present invention relates to bifunctional compounds, 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 present invention is directed to compounds, which contain on one end a VHL ligand which binds to the 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. The present invention exhibits a broad range of pharmacological activities associated with compounds according to the present invention, consistent with the degradation/inhibition of targeted polypeptides.
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公开(公告)号:US20210171470A1
公开(公告)日:2021-06-10
申请号:US16888484
申请日:2020-05-29
Applicant: Arvinas Operations, Inc.
Inventor: Andrew P. Crew , Keith R. Hornberger , Lawrence B. Snyder , Kurt Zimmermann , Jing Wang , Michael Berlin , Craig M. Crews , Hanqing Dong
IPC: C07D233/42 , A61K31/166 , C07D211/76 , C07D241/04 , C07D231/12 , C07D213/72 , C07D205/04 , C07D237/08 , C07D239/24 , C07D221/20 , A61K31/277 , A61K47/10 , A61K31/02 , A61K31/497 , C07D209/48 , C07D401/14 , A61K45/06
Abstract: The present disclosure relates to bifunctional compounds, which find utility to degrade and (inhibit) Androgen Receptor. In particular, the present disclosure is directed to compounds, which contain on one end a cereblon ligand which binds to the E3 ubiquitin ligase and on the other end a moiety which binds Androgen Receptor, such that Androgen Receptor is placed in proximity to the ubiquitin ligase to effect degradation (and inhibition) of Androgen Receptor. The present disclosure exhibits a broad range of pharmacological activities associated with compounds according to the present disclosure, consistent with the degradation/inhibition of Androgen Receptor.
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公开(公告)号:US20210040044A1
公开(公告)日:2021-02-11
申请号:US17006193
申请日:2020-08-28
Applicant: Arvinas Operations, Inc.
Inventor: Andrew P. Crew , Keith R. Hornberger , Lawrence B. Snyder , Kurt Zimmermann , Jing Wang , Michael Berlin , Hanqing Dong
IPC: C07D233/42 , C07D221/20 , C07D211/76 , C07D205/04 , C07D239/24 , A61K45/06 , C07D209/48 , C07D237/08 , C07D213/72 , A61K31/02 , C07D401/14 , A61K31/166 , A61K31/277 , C07D231/12 , C07D241/04 , A61K31/497 , A61K47/10
Abstract: The present disclosure relates to bifunctional compounds, which find utility to degrade and (inhibit) Androgen Receptor. In particular, the present disclosure is directed to compounds, which contain on one end a cereblon ligand which binds to the E3 ubiquitin ligase and on the other end a moiety which binds Androgen Receptor, such that Androgen Receptor is placed in proximity to the ubiquitin ligase to effect degradation (and inhibition) of Androgen Receptor. The present disclosure exhibits a broad range of pharmacological activities associated with compounds according to the present disclosure, consistent with the degradation/inhibition of Androgen Receptor.
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44.
公开(公告)号:US10899742B1
公开(公告)日:2021-01-26
申请号:US16744414
申请日:2020-01-16
Applicant: Arvinas Operations, Inc.
Inventor: Andrew P. Crew , Yimin Qian , Hanqing Dong , Jing Wang
IPC: A61K31/496 , C07D401/14 , A61K47/54 , A61P15/00 , A61P35/00 , A61K31/454 , A61K31/4545 , A61K31/4725 , A61K31/497 , A61K31/501 , A61K31/519 , A61K31/5386 , A61K31/551 , A61K38/05 , A61K38/06 , A61K45/06 , 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: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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公开(公告)号:US11952347B2
公开(公告)日:2024-04-09
申请号:US17539679
申请日:2021-12-01
Applicant: Arvinas Operations, Inc.
Inventor: Andrew P. Crew , Lawrence B. Snyder , Jing Wang
IPC: C07D401/14 , A61K31/02 , A61K31/166 , A61K31/277 , A61K31/496 , A61K31/497 , A61K31/501 , A61K31/506 , A61K45/06 , A61K47/10 , C07D205/04 , C07D209/48 , C07D211/76 , C07D213/72 , C07D221/20 , C07D231/12 , C07D233/42 , C07D237/08 , C07D239/24 , C07D241/04 , C07D401/04
CPC classification number: C07D233/42 , A61K31/02 , A61K31/166 , A61K31/277 , A61K31/496 , A61K31/497 , A61K31/501 , A61K31/506 , A61K45/06 , A61K47/10 , C07D205/04 , C07D209/48 , C07D211/76 , C07D213/72 , C07D221/20 , C07D231/12 , C07D237/08 , C07D239/24 , C07D241/04 , C07D401/04 , C07D401/14
Abstract: The present disclosure relates to bifunctional compounds, which find utility to degrade (and inhibit) Androgen Receptor. In particular, the present disclosure is directed to compounds, which contain on one end a cereblon ligand which binds to the E3 ubiquitin ligase and on the other end a moiety which binds Androgen Receptor, such that Androgen Receptor is placed in proximity to the ubiquitin ligase to effect degradation (and inhibition) of Androgen Receptor. The present disclosure exhibits a broad range of pharmacological activities associated with compounds according to the present disclosure, consistent with the degradation/inhibition of Androgen Receptor.
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公开(公告)号:US20240076295A1
公开(公告)日:2024-03-07
申请号:US18108045
申请日:2023-02-10
Applicant: Arvinas Operations, Inc. , Genentech, Inc.
Inventor: Andrew P. Crew , Jing Wang , Michael Berlin , Peter Dragovich , Huifen Chen , Leanna Staben
IPC: C07D417/14 , A61K47/10 , A61K47/18 , A61K47/22 , A61K47/54 , A61P35/00 , C07D413/14
CPC classification number: C07D417/14 , A61K47/10 , A61K47/18 , A61K47/22 , A61K47/545 , A61P35/00 , C07D413/14
Abstract: The present disclosure relates to bifunctional compounds, which find utility as modulators of SMARCA2 or BRM (target protein). In particular, the present disclosure is directed to bifunctional compounds, which contain on one end a ligand that binds to the Von Hippel-Lindau 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:US20230086457A1
公开(公告)日:2023-03-23
申请号:US17724987
申请日:2022-04-20
Applicant: ARVINAS OPERATIONS, INC.
Inventor: Michael Berlin , Andrew P. Crew , Hanqing Dong , John J. Flanagan
IPC: A61K31/4166 , A61K31/381 , A61K31/495 , C07D401/04 , C07D401/14 , C07D417/14
Abstract: The present disclosure relates to bifunctional compounds, which find utility as modulators of tau protein. In particular, the present disclosure is directed to bifunctional compounds, which contain on one end a VHL or cereblon ligand which binds to the E3 ubiquitin ligase and on the other end a moiety which binds tau protein, such that tau protein is placed in proximity to the ubiquitin ligase to effect degradation (and inhibition) of tau. The present disclosure exhibits a broad range of pharmacological activities associated with degradation/inhibition of tau protein. Diseases or disorders that result from aggregation or accumulation of tau protein are treated or prevented with compounds and compositions of the present disclosure.
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公开(公告)号:US20220315575A1
公开(公告)日:2022-10-06
申请号:US16932590
申请日:2020-07-17
Applicant: Arvinas Operations, Inc.
Inventor: Andrew P. Crew , Michael Berlin , Hanqing Dong , Alexey Ishchenko , Angela M. Cacace , Julian T. Chandler
IPC: C07D417/14 , A61K47/54 , C07D401/04 , C07D487/04
Abstract: The present disclosure relates to bifunctional compounds, which find utility as modulators of tau protein. In particular, the present disclosure is directed to bifunctional compounds, which contain on one end a VHL or cereblon ligand which binds to the E3 ubiquitin ligase and on the other end a moiety which binds tau protein, such that tau protein is placed in proximity to the ubiquitin ligase to effect degradation (and inhibition) of tau. The present disclosure exhibits a broad range of pharmacological activities associated with degradation/inhibition of tau protein. Diseases or disorders that result from aggregation or accumulation of tau protein are treated or prevented with compounds and compositions of the present disclosure.
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公开(公告)号:US11427548B2
公开(公告)日:2022-08-30
申请号:US16656526
申请日:2019-10-17
Applicant: Arvinas Operations, Inc.
Inventor: Andrew P. Crew , Hanqing Dong , Jing Wang , Xin Chen , Yimin Qian , Kurt Zimmermann , Michael Berlin , Lawrence Snyder
IPC: C07D233/86 , C07D417/14 , C07D413/12 , C07D417/12 , A61K45/06 , C07D491/107 , C07D471/10 , C07D235/02 , C07D401/04 , C07D401/08 , C07C255/54 , C07D237/24 , C07C271/24 , C07D241/28 , C07D239/42 , C07D231/14 , C07D213/82 , A61K31/4166 , A61K47/54 , A61K31/4439 , A61K31/4188 , A61K31/435 , A61K31/454 , A61K31/4184 , A61K31/277 , C07D413/14
Abstract: The present disclosure relates to bifunctional compounds, which find utility to degrade (and inhibit) Androgen Receptor. In particular, the present invention is directed to compounds, which contain on one end a VHL ligand which binds to the ubiquitin ligase and on the other end a moiety which binds Androgen Receptor such that Androgen Receptor is placed in proximity to the ubiquitin ligase to effect degradation (and inhibition) of Androgen Receptor. The present invention exhibits a broad range of pharmacological activities associated with compounds according to the present invention, consistent with the degradation/inhibition of Androgen Receptor.
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