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公开(公告)号:US20220213074A1
公开(公告)日:2022-07-07
申请号:US17610662
申请日:2020-05-13
Applicant: H. Lundbeck A/S
Inventor: Cheryl A. GRICE , Jeanne V. MOODY , Daniel J. BUZARD , Justin S. CISAR
IPC: C07D405/14 , C07D213/75
Abstract: Provided herein are compounds and compositions useful as modulators of ABHD12. Furthermore, the subject compounds and compositions are useful as immunotherapies in treating, for instance, cancer or infectious diseases.
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公开(公告)号:US20240018120A1
公开(公告)日:2024-01-18
申请号:US18252611
申请日:2021-11-12
Applicant: H. LUNDBECK A/S
Inventor: John J.M. WIENER , Cheryl A. GRICE , Daniel J. BUZARD , Justin S. CISAR , Olivia Delene WEBER , Amy ALLAN , Nicholas RAFFAELE , Jeanne V. MOODY , Michael B. SHAGHAFI
IPC: C07D401/12 , C07D405/12 , C07D413/12 , C07D401/14 , C07D487/04 , C07D471/04 , C07D221/20 , C07D417/12 , A61P29/00 , A61P25/08
CPC classification number: C07D401/12 , C07D405/12 , C07D413/12 , C07D401/14 , C07D487/04 , C07D471/04 , C07D221/20 , C07D417/12 , A61P29/00 , A61P25/08
Abstract: Provided herein are substituted 1,1,1,3,3,3-hexafluoropropan-2-yl 6-azaspiro[2.5]octane-6-carboxylate compounds and pharmaceutical compositions comprising said compounds. The compounds and compositions provided herein are useful as inhibitors of MAGL. Furthermore, the compounds and compositions as provided herein are useful for the treatment of diseases and disorders benefiting from the inhibition of MAGL.
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公开(公告)号:US20230357190A1
公开(公告)日:2023-11-09
申请号:US18311759
申请日:2023-05-03
Applicant: H. LUNDBECK A/S
Inventor: Thomas VETTER , John J.M. WIENER , Cheryl A. GRICE , Daniel J. BUZARD , Justin S. CISAR , Olivia Delene WEBER , Amy ALLAN , Nicholas RAFFAELE , Jeanne V. MOODY , Michael B. SHAGHAFI
IPC: C07D401/12
CPC classification number: C07D401/12 , C07B2200/13
Abstract: Described herein is new crystalline forms of the MAGL inhibitor 1,1,1,3,3,3-Hexafluoropropan-2-yl (S)-1-(pyridazin-3-ylcarbamoyl)-6-azaspiro[2.5]octane-6-carboxylate.
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公开(公告)号:US20230312499A1
公开(公告)日:2023-10-05
申请号:US18053582
申请日:2022-11-08
Applicant: H. Lundbeck A/S , THE SCRIPPS RESEARCH INSTITUTE
Inventor: Justin S. CISAR , Cheryl A. GRICE , Todd K. JONES , Micah J. NIPHAKIS , Jae Won CHANG , Kenneth M. LUM , Benjamin F. CRAVATT
IPC: C07D295/205 , C07C271/12 , C07D317/46 , C07D317/58 , C07D231/12 , C07D231/16 , C07D231/56 , C07D241/04 , C07D471/04 , C07D471/10 , C07D261/08 , C07D487/04 , C07D263/32 , C07D205/04 , C07D491/107 , C07D207/14 , C07D271/06 , C07D307/79 , C07D405/14 , C07D215/42 , C07D213/40 , A61P25/22 , C07D295/26 , C07D213/55 , C07D401/04 , C07D407/06 , C07D413/06 , C07C271/10 , C07D207/09 , C07D213/38 , C07D215/46 , C07D401/10 , C07D403/10 , C07D413/10
CPC classification number: C07D295/205 , C07C271/12 , C07D317/46 , C07D317/58 , C07D231/12 , C07D231/16 , C07D231/56 , C07D241/04 , C07D471/04 , C07D471/10 , C07D261/08 , C07D487/04 , C07D263/32 , C07D205/04 , C07D491/107 , C07D207/14 , C07D271/06 , C07D307/79 , C07D405/14 , C07D215/42 , C07D213/40 , A61P25/22 , C07D295/26 , C07D213/55 , C07D401/04 , C07D407/06 , C07D413/06 , C07C271/10 , C07D207/09 , C07D213/38 , C07D215/46 , C07D401/10 , C07D403/10 , C07D413/10
Abstract: This disclosure provides compounds and compositions which may be modulators of MAGL and/or ABHD6 and their use as medicinal agents, processes for their preparation, and pharmaceutical compositions that include disclosed compounds as at least one active agent. The disclosure also provides for method of treating a patient in need thereof, where the patient is suffering from post-traumatic stress disorder comprising administering a disclosed compound or composition.
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公开(公告)号:US20220153721A1
公开(公告)日:2022-05-19
申请号:US17524632
申请日:2021-11-11
Applicant: H. LUNDBECK A/S
Inventor: John J.M. WIENER , Cheryl A. GRICE , Daniel J. BUZARD , Justin S. CISAR , Olivia Delene WEBER , Amy ALLAN , Nicholas RAFFAELE , Jeanne MOODY , Michael B. SHAGHAFI
IPC: C07D401/12 , C07D405/12 , C07D413/12 , C07F9/6558 , C07D401/14 , C07D221/20 , C07D487/04 , C07D471/04 , C07D417/12 , A61P25/08 , A61P25/04
Abstract: Provided herein are substituted 1,1,1,3,3,3-hexafluoropropan-2-yl 6-azaspiro[2.5]octane-6-carboxylate compounds and pharmaceutical compositions comprising said compounds. The compounds and compositions provided herein are useful as inhibitors of MAGL. Furthermore, the compounds and compositions as provided herein are useful for the treatment of diseases and disorders benefiting from the inhibition of MAGL.
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