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公开(公告)号:US12226420B2
公开(公告)日:2025-02-18
申请号:US18433881
申请日:2024-02-06
Applicant: HMI MEDICAL INNOVATIONS, LLC
Inventor: Gerard M. Housey
IPC: A61K31/5377 , A61K31/166 , A61K31/175 , A61K31/195 , A61K31/27 , A61K31/415 , A61K31/4196 , A61K31/44 , A61K31/4436 , A61K31/444 , A61K31/47 , A61K31/4709 , A61K31/495 , A61K31/505 , A61K31/506 , A61K31/517 , A61K31/53 , C07C243/38 , C07D213/77 , C07D213/81 , C07D213/86 , C07D213/87 , C07D215/38 , C07D215/50 , C07D231/14 , C07D239/42 , C07D239/48 , C07D239/84 , C07D253/065 , C07D253/075 , C07D401/12 , C07D403/12 , C07D405/12 , C07D409/12 , G01N33/50 , G01N33/573 , G01N33/574
Abstract: This invention relates to agents that are inhibitors or activators of variant forms of endogenous proteins and novel methods of identifying such variants. Of particular interest are inhibitors and activators of endogenous protein variants, encoded by genes which have mutated, which variants often arise or are at least first identified as having arisen following exposure to a chemical agent which is known to be an inhibitor or activator of the corresponding unmutated endogenous protein.
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公开(公告)号:US12195413B2
公开(公告)日:2025-01-14
申请号:US17338643
申请日:2021-06-03
Applicant: Hoffmann-La Roche Inc.
Inventor: Georg Jaeschke , Lothar Lindemann , Antonio Ricci , Eric Vieira
IPC: C07C11/22 , A61K31/4166 , A61K31/4184 , A61K31/44 , A61K31/4439 , A61P1/00 , A61P1/04 , A61P25/00 , A61P25/04 , A61P25/16 , A61P25/18 , A61P25/22 , A61P25/24 , A61P25/28 , A61P29/00 , A61P43/00 , C07D213/81 , C07D401/04 , C07D403/04
Abstract: The present invention relates to ethynyl derivatives of formula I with variables as defined herein, or to a pharmaceutically acceptable acid addition salt thereof Compounds of formula I are metabotropic glutamate receptor antagonists (negative allosteric modulators) for use in the treatment of, e.g., anxiety and pain, depression, Fragile-X syndrome, autism spectrum disorders, Parkinson's disease, and gastroesophageal reflux disease (GERD).
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公开(公告)号:US12180175B2
公开(公告)日:2024-12-31
申请号:US17475486
申请日:2021-09-15
Applicant: Xi'an Easy Peptide Biotechnology Co., Ltd.
Inventor: Junfeng Zhao , Tao Liu
IPC: C07D317/28 , C07C67/03 , C07C67/08 , C07C201/12 , C07C231/02 , C07C269/06 , C07C327/22 , C07C327/26 , C07C329/04 , C07D213/81 , C07D213/83 , C07D215/48 , C07D295/185 , C07D333/70 , C07J1/00 , C07K5/06
Abstract: The present disclosure discloses a water-soluble ynamide coupling reagent and a method for using the water-soluble ynamide coupling reagent in the synthesis of amide, polypeptide, ester and thioester compound. The ynamide coupling reagent has the structure represented by the following formula (I): and in the formula (I), R is one selected from the group consisting of methylsulfonyl, benzenesulfonyl, p-toluenesulfonyl, trifluoroacetyl and other electron withdrawing groups.
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公开(公告)号:US12180163B2
公开(公告)日:2024-12-31
申请号:US17483232
申请日:2021-09-23
Applicant: CORTEVA AGRISCIENCE LLC
Inventor: Brian A. Loy , Nicolaas Vermeulen , Brannon Sam , Kevin G. Meyer , Chenglin Yao , Nicholas R. Babij , Jeff Petkus
IPC: C07D213/81 , A01N37/02 , A01N43/10 , A01N43/40 , A01N43/84 , A01N47/18 , C07B53/00 , C07C229/28 , C07C271/18 , C07D213/83 , C07D333/08 , C07D409/12 , C07D498/04
Abstract: This disclosure relates to picolinamides of Formula I and their use as fungicides.
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公开(公告)号:US20240409580A1
公开(公告)日:2024-12-12
申请号:US18809625
申请日:2024-08-20
Applicant: Siemens Medical Solutions USA, Inc.
Inventor: Eric Wang , Hartmuth C. Kolb , Anna Katrin Szardenings , Changhui Liu , Joseph C. Walsh , Gang Chen , Anjana Sinha , Dhanalakshmi Kasi , Chul Yu , Umesh B. Gangadharmath , Wei Zhang , Tieming Zhao , Vani P. Mocharla
IPC: C07K5/02 , A61K38/00 , A61K51/04 , A61K51/08 , C07D207/16 , C07D209/48 , C07D213/81 , C07D213/82 , C07D233/78 , C07D233/96 , C07D239/60 , C07D249/04 , C07D249/06 , C07D251/30 , C07D263/34 , C07D277/56 , C07D401/12 , C07D403/06 , C07D403/12 , C07D405/12 , C07K5/062 , C07K5/072
Abstract: Compounds for targeting and agents for imaging, prostate-specific membrane antigen (PSMA) are disclosed. Methods of synthesizing compounds and imaging agents, as well as methods for imaging PSMA are also disclosed. The imaging agents disclosed are suitable for PET and SPECT imaging.
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公开(公告)号:US20240336568A1
公开(公告)日:2024-10-10
申请号:US18742052
申请日:2024-06-13
Applicant: Akebia Therapeutics, Inc.
Inventor: Thomas P. BLAISDELL , Paul E. FLEMING
IPC: C07D213/81 , A61K31/4418 , A61K31/4436 , A61K31/4439 , A61K31/444 , A61K31/4545 , A61K31/4709 , A61K31/4725 , A61K31/498 , A61K31/502 , A61K31/5377 , C07D213/84 , C07D401/04 , C07D401/10 , C07D401/12 , C07D401/14 , C07D417/04 , C07D471/04 , C07D495/04
CPC classification number: C07D213/81 , A61K31/4418 , A61K31/4436 , A61K31/4439 , A61K31/444 , A61K31/4545 , A61K31/4709 , A61K31/4725 , A61K31/498 , A61K31/502 , A61K31/5377 , C07D213/84 , C07D401/04 , C07D401/10 , C07D401/12 , C07D401/14 , C07D417/04 , C07D471/04 , C07D495/04
Abstract: The present invention provides, in part, compounds and methods for treating diseases mediated by PHD1 activity (e.g., ischemia reperfusion injury (including but not limited to stroke, myocardial infarction, and acute kidney injury) inflammatory bowel disease, cancer (including colorectal cancer) and liver disease) comprising administering to a subject to a subject a compound of Formula (I), and sub-formulas thereof:
or a pharmaceutically acceptable salt thereof.-
公开(公告)号:US20240325361A1
公开(公告)日:2024-10-03
申请号:US18500471
申请日:2023-11-02
Applicant: Akebia Therapeutics, Inc.
Inventor: Alexander Smith , Gurudatt Ajay Chandorkar , Ene Ikpong Ette , Bradley John Maroni , Charlotte Suzanne Hartman , Ramin Farzaneh-Far , Jula Kern Inrig
IPC: A61K31/4418 , A61K9/20 , A61K9/28 , A61K31/16 , C07D213/81
CPC classification number: A61K31/4418 , A61K9/2009 , A61K9/2013 , A61K9/2054 , A61K9/2059 , A61K9/2866 , A61K31/16 , C07D213/81
Abstract: Provided herein are specific doses of, and dosing regimens for, using a HIF prolyl hydroxylase inhibitor in treating or preventing anemia, such as anemia secondary to or associated with chronic kidney disease, anemia secondary to or associated with non-dialysis dependent chronic kidney disease anemia associated with or resulting from chemotherapy, or anemia associated with AIDS.
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公开(公告)号:US20240317732A1
公开(公告)日:2024-09-26
申请号:US18262941
申请日:2022-01-28
Applicant: THE UNITED STATES OF AMERICA AS REPRESENTED BY THE SECRETARY, DEPARTMENT OF HEALTH AND HUMAN SERVICE
Inventor: Kylie J. Walters , Xiuxiu LU , Nadya I. Tarasova , Eric Rolf SWENSON , Venkatareddy SABBASANI , Beverly Ann MOCK , Snehal GAIKWAD , Deborah CITRIN , Monika CHANDRAVANSHI
IPC: C07D417/14 , C07C255/44 , C07C311/46 , C07D213/81 , C07D401/14 , C07D403/12 , C07D417/12
CPC classification number: C07D417/14 , C07C255/44 , C07C311/46 , C07D213/81 , C07D401/14 , C07D403/12 , C07D417/12
Abstract: In accordance with the purpose(s) of the present disclosure, as embodied and broadly described herein, the disclosure, in one aspect, relates to scaffold molecules having anti-hRPN13 activity, proteolysis targeting chimeras (PROTACs) incorporating the same, methods of making same, pharmaceutical compositions comprising same, and methods of treating cancers involving aberrant hRpn13 activity and/or the presence of hRpn13-Pru/hRpn13 or variants thereof using the same.
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公开(公告)号:US20240246908A1
公开(公告)日:2024-07-25
申请号:US18555291
申请日:2022-04-14
Applicant: ORION CORPORATION
Inventor: Marko AHLMARK , David DIN BELLE , Dimitris NOUTSIAS , Pekka PIETIKÄINEN , Petteri RUMMAKKO , Julius SIPILÄ , Gerd WOHLFAHRT
IPC: C07D207/277 , A61K31/197 , A61K31/381 , A61K31/382 , A61K31/397 , A61K31/40 , A61K31/4015 , A61K31/4025 , A61K31/407 , A61K31/41 , A61K31/4155 , A61K31/4166 , A61K31/421 , A61K31/4245 , A61K31/425 , A61K31/427 , A61K31/429 , A61K31/4412 , A61K31/4439 , A61K31/45 , A61K31/4525 , A61K31/453 , A61K31/4545 , A61K31/4709 , A61K31/495 , A61K31/496 , C07C237/04 , C07D205/04 , C07D205/08 , C07D207/16 , C07D207/24 , C07D207/263 , C07D211/78 , C07D213/81 , C07D233/32 , C07D257/04 , C07D263/24 , C07D275/03 , C07D285/00 , C07D333/48 , C07D335/02 , C07D401/12 , C07D401/14 , C07D403/04 , C07D403/06 , C07D403/12 , C07D405/04 , C07D405/12 , C07D405/14 , C07D413/12 , C07D487/04 , C07D513/04
CPC classification number: C07D207/277 , A61K31/197 , A61K31/381 , A61K31/382 , A61K31/397 , A61K31/40 , A61K31/4015 , A61K31/4025 , A61K31/407 , A61K31/41 , A61K31/4155 , A61K31/4166 , A61K31/421 , A61K31/4245 , A61K31/425 , A61K31/427 , A61K31/429 , A61K31/4412 , A61K31/4439 , A61K31/45 , A61K31/4525 , A61K31/453 , A61K31/4545 , A61K31/4709 , A61K31/495 , A61K31/496 , C07C237/04 , C07D205/04 , C07D205/08 , C07D207/16 , C07D207/24 , C07D207/263 , C07D211/78 , C07D213/81 , C07D233/32 , C07D257/04 , C07D263/24 , C07D275/03 , C07D285/00 , C07D333/48 , C07D335/02 , C07D401/12 , C07D401/14 , C07D403/04 , C07D403/06 , C07D403/12 , C07D405/04 , C07D405/12 , C07D405/14 , C07D413/12 , C07D487/04 , C07D513/04
Abstract: The present invention relates to a compound of formula (I)
wherein A, Z, L, R1, R2, R3, R4, R5 and R33 are as defined in claim 1, or a pharmaceutically acceptable salt thereof. The compounds of formula (I) possess utility as inhibitors of TEAD. The compounds are useful as medicaments in the treatment of diseases or conditions wherein inhibition of TEAD is desired, such as cancer and chronic pain.-
公开(公告)号:US20240180916A1
公开(公告)日:2024-06-06
申请号:US18433881
申请日:2024-02-06
Applicant: HMI MEDICAL INNOVATIONS, LLC
Inventor: Gerard M. HOUSEY
IPC: A61K31/5377 , A61K31/166 , A61K31/175 , A61K31/195 , A61K31/27 , A61K31/415 , A61K31/4196 , A61K31/44 , A61K31/4436 , A61K31/444 , A61K31/47 , A61K31/4709 , A61K31/495 , A61K31/505 , A61K31/506 , A61K31/517 , A61K31/53 , C07C243/38 , C07D213/77 , C07D213/81 , C07D213/86 , C07D213/87 , C07D215/38 , C07D215/50 , C07D231/14 , C07D239/42 , C07D239/48 , C07D239/84 , C07D253/065 , C07D253/075 , C07D401/12 , C07D403/12 , C07D405/12 , C07D409/12 , G01N33/50 , G01N33/573 , G01N33/574
CPC classification number: A61K31/5377 , A61K31/166 , A61K31/175 , A61K31/195 , A61K31/27 , A61K31/415 , A61K31/4196 , A61K31/44 , A61K31/4436 , A61K31/444 , A61K31/47 , A61K31/4709 , A61K31/495 , A61K31/505 , A61K31/506 , A61K31/517 , A61K31/53 , C07C243/38 , C07D213/77 , C07D213/81 , C07D213/86 , C07D213/87 , C07D215/38 , C07D215/50 , C07D231/14 , C07D239/42 , C07D239/48 , C07D239/84 , C07D253/065 , C07D253/075 , C07D401/12 , C07D403/12 , C07D405/12 , C07D409/12 , G01N33/5011 , G01N33/502 , G01N33/5041 , G01N33/573 , G01N33/574 , G01N2500/00 , G01N2500/10
Abstract: This invention relates to agents that are inhibitors or activators of variant forms of endogenous proteins and novel methods of identifying such variants. Of particular interest are inhibitors and activators of endogenous protein variants, encoded by genes which have mutated, which variants often arise or are at least first identified as having arisen following exposure to a chemical agent which is known to be an inhibitor or activator of the corresponding unmutated endogenous protein.
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