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公开(公告)号:US20250042915A1
公开(公告)日:2025-02-06
申请号:US18743475
申请日:2024-06-14
Applicant: Gilead Sciences, Inc.
Inventor: Stephen E. Ammann , Xinpei Cai , Eda Y. Canales , Weng K. Chang , Gregory F. Chin , Henok H. Kinfe , Scott E. Lazerwith , Jessica L. McKinley , Michael R. Mish , Devan Naduthambi , Jason K. Perry , Kevin X. Rodriguez , Scott D. Schroeder , Christopher J. Swank , Joshua J. Van Veldhuizen
IPC: C07D495/04 , A61P31/14 , C07D401/04 , C07D401/14 , C07D405/14 , C07D409/14 , C07D413/14 , C07D417/14 , C07D471/04 , C07D487/04 , C07D487/10 , C07D491/107 , C07D491/113 , C07D498/04 , C07D513/04 , C07D519/00
Abstract: The present disclosure relates to compounds of Formula I: and pharmaceutically acceptable salts thereof, pharmaceutical compositions thereof, useful in the treatment of treating viral infections, for example, coronaviridae infections.
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公开(公告)号:US20240294539A1
公开(公告)日:2024-09-05
申请号:US18626788
申请日:2024-04-04
Applicant: Bayer Aktiengesellschaft
Inventor: Thomas HIMMLER , Peter BRUECHNER , Werner LINDNER , Julia Johanna HAHN , Wahed Ahmed MORADI , Reiner FISCHER , Michael DOCKNER
IPC: C07D491/113 , C07C229/48 , C07C233/52 , C07D209/54
CPC classification number: C07D491/113 , C07C229/48 , C07C233/52 , C07D209/54 , C07C2601/14 , C07C2601/16
Abstract: The present invention relates to a novel process for preparing substituted cyclohexane amino acid esters and spiroketal-substituted cyclic keto-enols, and to novel intermediates or starting compounds that are passed through or used in the process according to the invention.
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公开(公告)号:US12076306B2
公开(公告)日:2024-09-03
申请号:US18144890
申请日:2023-05-09
Applicant: Alkermes Pharma Ireland Limited
Inventor: Tarek A. Zeidan , Scott Duncan , Christopher P. Hencken , Thomas Andrew Wynn , Carlos N. Sanrame
IPC: C07C235/88 , A61K31/225 , C07C219/08 , C07C229/16 , C07C233/18 , C07C233/91 , C07C317/18 , C07C317/28 , C07D207/06 , C07D207/40 , C07D209/52 , C07D211/06 , C07D211/38 , C07D295/088 , C07D491/113
CPC classification number: A61K31/225 , C07C219/08 , C07C229/16 , C07C233/18 , C07C233/91 , C07C235/88 , C07C317/18 , C07C317/28 , C07D207/06 , C07D207/40 , C07D209/52 , C07D211/06 , C07D211/38 , C07D295/088 , C07D491/113
Abstract: The present invention provides compounds of formula (I), and pharmaceutical compositions thereof.
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公开(公告)号:US20240246910A1
公开(公告)日:2024-07-25
申请号:US18405058
申请日:2024-01-05
Applicant: Sensorium Therapeutics, Inc.
Inventor: Jacob M. Hooker , Michael S. Placzek
IPC: C07D209/12 , C07D401/12 , C07D405/12 , C07D409/12 , C07D475/04 , C07D491/113 , C07D491/20 , C07D495/04 , C07D495/10 , C07D497/10 , C07D498/10 , C07D519/00 , C07F7/18
CPC classification number: C07D209/12 , C07D401/12 , C07D405/12 , C07D409/12 , C07D475/04 , C07D491/113 , C07D491/20 , C07D495/04 , C07D495/10 , C07D497/10 , C07D498/10 , C07D519/00 , C07F7/1804
Abstract: Disclosed are prodrug compounds that can be converted to mesembrine under biologically relevant conditions, such as hydrolysis in vivo; and related methods of preparing and using these compounds. Stable preparations of isolated mesembrine stereoisomers are also provided.
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公开(公告)号:US12042541B2
公开(公告)日:2024-07-23
申请号:US18194540
申请日:2023-03-31
Applicant: ARBUTUS BIOPHARMA CORPORATION
Inventor: Muthiah Manoharan , Muthusamy Jayaraman , Kallanthottathil G. Rajeev , Laxman Eltepu , Steven Ansell , Jianxin Chen
IPC: A61K47/44 , A61K9/127 , A61K31/7088 , A61K31/713 , A61K39/00 , A61K39/39 , A61K47/10 , A61K47/18 , A61K47/20 , A61K47/28 , C07C229/08 , C07C229/30 , C07C237/16 , C07C251/38 , C07C251/78 , C07C271/12 , C07C271/20 , C07C323/25 , C07D203/10 , C07D317/28 , C07D317/44 , C07D317/46 , C07D317/72 , C07D319/06 , C07D405/12 , C07D491/056 , C07D491/113 , C12N15/11 , C12N15/113
CPC classification number: A61K47/44 , A61K9/1272 , A61K31/7088 , A61K31/713 , A61K39/00 , A61K39/39 , A61K47/10 , A61K47/18 , A61K47/20 , A61K47/28 , C07C229/08 , C07C229/30 , C07C237/16 , C07C251/38 , C07C251/78 , C07C271/12 , C07C271/20 , C07C323/25 , C07D203/10 , C07D317/28 , C07D317/44 , C07D317/46 , C07D317/72 , C07D319/06 , C07D405/12 , C07D491/056 , C07D491/113 , C12N15/111 , C12N15/113 , A61K2039/55555 , A61K2039/55561 , C12N2310/14 , C12N2310/3515 , C12N2320/32 , Y02A50/30
Abstract: The present invention provides lipids that are advantageously used in lipid particles for the in vivo delivery of therapeutic agents to cells. In particular, the invention provides lipids having the following structure
wherein:
R1 and R2 are each independently for each occurrence optionally substituted C10-C30 alkyl, optionally substituted C10-C30 alkenyl, optionally substituted C10-C30 alkynyl, optionally substituted C10-C30 acyl, or -linker-ligand; R3 is H, optionally substituted C1-C10 alkyl, optionally substituted C2-C10 alkenyl, optionally substituted C2-C10 alkynyl, alkylhetrocycle, alkylphosphate, alkylphosphorothioate, alkylphosphorodithioate, alkylphosphonates, alkylamines, hydroxyalkyls, ω-aminoalkyls, ω-(substituted)aminoalkyls, ω-phosphoalkyls, ω-thiophosphoalkyls, optionally substituted polyethylene glycol (PEG, mw 100-40K), optionally substituted mPEG (mw 120-40K), heteroaryl, heterocycle, or linker-ligand; and E is C(O)O or OC(O).-
公开(公告)号:US20240116897A1
公开(公告)日:2024-04-11
申请号:US18274864
申请日:2022-01-21
Inventor: Kwang Rok KIM , Kwan Young JEONG , Hee Jung JUNG , Doyoun KIM , Junmi LEE , Sang Dal RHEE , Kyu Myung LEE
IPC: C07D403/12 , A61P35/00 , C07D235/32 , C07D417/04 , C07D417/12 , C07D417/14 , C07D471/10 , C07D487/08 , C07D491/113 , C07D513/04
CPC classification number: C07D403/12 , A61P35/00 , C07D235/32 , C07D417/04 , C07D417/12 , C07D417/14 , C07D471/10 , C07D487/08 , C07D491/113 , C07D513/04
Abstract: The present invention relates to a benzothiazole or benzimidazole derivative, a pharmaceutically acceptable salt thereof, and a pharmaceutical composition comprising same as an active ingredient for prevention or treatment of SIRTUIN 7 protein-related diseases. With excellent inhibitory activity against SIRTUIN 7 protein the derivative can be used for preventing or treating SIRTUIN 7 protein-related diseases.
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公开(公告)号:US20240101549A1
公开(公告)日:2024-03-28
申请号:US18257123
申请日:2021-12-16
Applicant: AstraZeneca AB
Inventor: Jonas BRÅNALT , Björn HOLM , Maria JOHANSSON , Olle KARLSSON , Daniel Laurent KNERR , Anneli NORDQVIST , Robert John SHEPPARD , Marianne SWANSON , Anna TOMBERG
IPC: C07D417/14 , C07D493/10 , C07D487/04 , C07D491/107 , C07D491/113 , C07D487/10 , C07D498/08 , C07D495/10 , A61P1/16
CPC classification number: C07D417/14 , C07D493/10 , C07D487/04 , C07D491/107 , C07D491/113 , C07D487/10 , C07D498/08 , C07D495/10 , A61P1/16
Abstract: Compounds having the structure of Formula (I): and pharmaceutically acceptable salts thereof, wherein X1, R1, R2, R3, R4, R5 and R6 are as defined in the specification; pharmaceutical compositions comprising such compounds and salts; use of such compounds and salts to treat or prevent Prolyl endopeptidase fibroblast activation protein (FAP)-mediated conditions; kits comprising such compounds and salts; and methods for manufacturing such compounds and salts.
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公开(公告)号:US20230150993A1
公开(公告)日:2023-05-18
申请号:US17930352
申请日:2022-09-07
Applicant: Merck Patent GmbH , Vertex Pharmaceuticals Incorporated
Inventor: Henry YU , Michael Clark , Guy Bemis , Micheal Boyd , Kishan Chandupatla , Philip Collier , Hongbo Deng , Huijun Dong , Warren Dorsch , Russell R. Hoover , Mac Arthur Johnson, JR. , Shashank Kulkarni , Marina Penney , Steven Ronkin , Darin Takemoto , Qing Tang , Nathan D. Waal , Tiansheng Wang , David J. Lauffer , Pan Li
IPC: C07D413/14 , A61P35/00 , C07D417/14 , C07D491/107 , C07D401/14 , C07D413/04 , C07D491/113 , C07D403/04
CPC classification number: C07D413/14 , A61P35/00 , C07D417/14 , C07D491/107 , C07D401/14 , C07D413/04 , C07D491/113 , C07D403/04
Abstract: The present invention provides compounds of Formula I′, or pharmaceutically acceptable salts thereof, pharmaceutical compositions thereof, and methods of use thereof for treating cellular proliferative disorders (e.g., cancer).
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公开(公告)号:US11555012B2
公开(公告)日:2023-01-17
申请号:US16677768
申请日:2019-11-08
Applicant: Nimbus Artemis, Inc.
Inventor: Silvana Marcel Leit de Moradei , Eric Therrien
IPC: C07C311/29 , C07C311/21 , C07D491/113 , C07D295/135 , C07D333/20 , C07D257/04 , C07D295/10 , C07D205/04 , C07D277/34 , C07D209/80 , C07D231/38 , C07D263/32 , C07D401/12 , C07D413/06 , C07D401/04 , C07D409/12 , C07D213/04
Abstract: The present invention provides compounds useful as inhibitors of ATP citrate lyase (ACLY), compositions thereof, and methods of using the same.
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公开(公告)号:US20230002393A1
公开(公告)日:2023-01-05
申请号:US17620346
申请日:2020-05-20
Applicant: BEIJING BENICALL BIOTECH CO., LTD.
Inventor: Zhengying Pan , Rui Zhang , Zude Qi
IPC: C07D487/04 , C07D519/00 , C07D491/107 , C07D491/113
Abstract: Disclosed in the present application are a compound of general formula (I) capable of being used as a CDK kinase (in particular, CDK4/6 kinase) inhibitor, and a salt thereof, wherein all variates are defined as the present text. The compound can be used for treating or preventing diseases such as cancer. The present application further relates to a pharmaceutical composition comprising the compound of formula (I).
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