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公开(公告)号:US12077509B2
公开(公告)日:2024-09-03
申请号:US18213055
申请日:2023-06-22
Applicant: Arvinas Operations, Inc.
Inventor: Hanqing Dong , Keith R. Hornberger , Lawrence B. Snyder
IPC: A61K31/166 , A61K31/02 , 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 , C07D401/14
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:US11964945B2
公开(公告)日:2024-04-23
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 , Hanqing Dong
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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33.
公开(公告)号:US11857519B2
公开(公告)日:2024-01-02
申请号:US17354941
申请日:2021-06-22
Applicant: Arvinas Operations, Inc.
Inventor: Andrew P. Crew , Lawrence B. Snyder , Jing Wang , Hanqing Dong , Yimin Qian , Michael Berlin
IPC: A61K31/166 , A61K31/405 , A61K47/54 , A61P35/00 , A61K38/45 , C12N9/10 , A61K31/351 , C07D471/04 , C07D401/14 , C07D405/14 , C07D405/12 , C07D417/14 , C07D409/14 , A61K47/55
CPC classification number: A61K31/166 , A61K31/351 , A61K31/405 , A61K38/45 , A61K47/545 , A61K47/55 , A61K47/555 , A61P35/00 , C07D401/14 , C07D405/12 , C07D405/14 , C07D409/14 , C07D417/14 , C07D471/04 , C12N9/1007 , C12Y201/01043
Abstract: The present disclosure relates to bifunctional compounds, which find utility as modulators of enhancer of zeste homolog 2 (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, 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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34.
公开(公告)号:US20230084249A1
公开(公告)日:2023-03-16
申请号:US17506324
申请日:2021-10-20
Applicant: Arvinas Operations, Inc.
Inventor: Michael Berlin , Andrew P. Crew , Hanqing Dong , Keith R. Hornberger , Lawrence B. Snyder , Jing Wang , Kurt Zimmermann
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:US20220402907A1
公开(公告)日:2022-12-22
申请号:US17360699
申请日:2021-06-28
Applicant: Arvinas Operations, Inc.
Inventor: Andrew P. Crew , Keith R. Hornberger , Jing Wang , Hanqing Dong
IPC: C07D417/14 , A61P35/00 , C07D401/14 , C07D413/14 , C07D471/04
Abstract: The present disclosure relates to bifunctional compounds, which find utility as modulators of Kirsten rat sarcoma protein (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, 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, accumulation, and/or overactivation 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:US20220395576A1
公开(公告)日:2022-12-15
申请号:US17721916
申请日:2022-04-15
Applicant: Arvinas Operations, Inc.
Inventor: Michael Berlin , Hanqing Dong , Dan Sherman , Lawrence B. Snyder , Jing Wang , Wei Zhang
Abstract: Bifunctional compounds, which find utility as modulators of B-cell lymphoma 6 protein (BCL6; target protein), are described herein. In particular, the bifunctional compounds of the present disclosure contain on one end a cereblon ligand that 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 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 aggregation or accumulation of the target protein are treated or prevented with compounds and compositions of the present disclosure.
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37.
公开(公告)号:US20220388984A1
公开(公告)日:2022-12-08
申请号:US17359424
申请日:2021-06-25
Applicant: Arvinas Operations, Inc.
Inventor: Andrew P. Crew , Hanqing Dong , Keith R. Hornberger , Yimin Quian , Jing Wang
IPC: C07D401/14 , A61K47/54 , A61P15/00 , A61P35/00 , A61K31/454 , A61K31/4545 , A61K31/4725 , A61K31/496 , 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
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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38.
公开(公告)号:US20220378726A1
公开(公告)日:2022-12-01
申请号:US17354941
申请日:2021-06-22
Applicant: Arvinas Operations, Inc.
Inventor: Andrew P. Crew , Lawrence B. Snyder , Jing Wang , Hanqing Dong , Yimin Qian , Michael Berlin
IPC: A61K31/166 , A61K31/405 , A61K47/54 , A61P35/00 , A61K38/45 , C12N9/10 , A61K31/351 , C07D471/04 , C07D401/14 , C07D405/14 , C07D405/12 , C07D417/14 , C07D409/14 , A61K47/55
Abstract: The present disclosure relates to bifunctional compounds, which find utility as modulators of enhancer of zeste homolog 2 (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, 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: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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