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公开(公告)号:US20210323991A1
公开(公告)日:2021-10-21
申请号:US17251964
申请日:2019-06-13
Applicant: BRISTOL-MYERS SQUIBB COMPANY
Inventor: Richard A. Hartz , Li Xu , David S. Yoon , Alicia Regueiro-Ren , Prasada Rao Jalagam , Manoranjan Panda , Satheesh Kesavan Nair
Abstract: The present disclosure relates to compounds of Formula (1), which inhibit Gal-3, and include pharmaceutically acceptable salts, compositions comprising such compounds, and methods making and using such compounds and compositions.
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公开(公告)号:US20210147408A1
公开(公告)日:2021-05-20
申请号:US16650403
申请日:2018-09-27
Applicant: BRISTOL-MYERS SQUIBB COMPANY
Inventor: Prasada Rao Jalagam , Satheesh Kesavan Nair , Manoranjan Panda , Ramakanth SARABU , Jacob SWIDORSKI , Brett R. BENO , Alicia Regueiro-Ren
IPC: C07D417/14 , C07D405/14
Abstract: The present disclosure relates to compounds of formula I, which inhibit Gal-3, and include pharmaceutically acceptable salts, compositions comprising such compounds, and methods using and making such compounds and compositions.
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公开(公告)号:US20200339550A1
公开(公告)日:2020-10-29
申请号:US16928079
申请日:2020-07-14
Applicant: BRISTOL-MYERS SQUIBB COMPANY
Inventor: Navnath Dnyanoba Yadav , Rajeev S. Bhide , Rajesh Onkardas Bora , Prashantha Gunaga , Manoranjan Panda , Eldon Scott Priestley , Jeremy Richter
IPC: C07D405/14 , C07D413/14 , C07D417/14 , C07D487/04
Abstract: Disclosed are compounds of Formula (I) or a salt thereof, wherein R1 is: each W is independently NR1b or O; Z is a bond or CHR1d; and R1, R2, Rd, R3a, R3b, L1, B, V, Y, and n are defined herein. Also disclosed are methods of using such compounds as inhibitors of ROMK, and pharmaceutical compositions comprising such compounds. These compounds are useful in treating cardiovascular diseases.
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公开(公告)号:US20190127380A1
公开(公告)日:2019-05-02
申请号:US16094288
申请日:2017-04-19
Applicant: BRISTOL-MYERS SQUIBB COMPANY
Inventor: Prashantha Gunaga , Jeremy Richter , Navnath Dnyanoba Yadav , Manoranjan Panda , Sreenivasulu Godesi
IPC: C07D487/04 , C07D407/04 , C07D471/04 , C07D407/06 , C07D413/14 , C07D519/00
Abstract: Disclosed are compounds of Formula (I), or a salt thereof, wherein: X is CR4 or N; Y is CR4 or N, provided that Y is N only if X is N; R1 is Formulae (A) or (B); each W is independently NR1b or O; Z is a bond or CHR1d; and R1, R2, R3, R4, L1, R1a, R1b, R1c, and n are defined herein. Also disclosed are methods of using such compounds as inhibitors of ROMK, and pharmaceutical compositions comprising such compounds. These compounds are useful in treating cardiovascular diseases.
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公开(公告)号:US11970511B2
公开(公告)日:2024-04-30
申请号:US17251964
申请日:2019-06-13
Applicant: BRISTOL-MYERS SQUIBB COMPANY
Inventor: Richard A. Hartz , Li Xu , David S. Yoon , Alicia Regueiro-Ren , Prasada Rao Jalagam , Manoranjan Panda , Satheesh Kesavan Nair
Abstract: The present disclosure relates to compounds of Formula (1), which inhibit Gal-3, and include pharmaceutically acceptable salts, compositions comprising such compounds, and methods making and using such compounds and compositions.
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公开(公告)号:USRE49700E1
公开(公告)日:2023-10-17
申请号:US17183286
申请日:2021-02-23
Applicant: Bristol-Myers Squibb Company
Inventor: Navnath Dnyanoba Yadav , Rajeev S. Bhide , Rajesh Onkardas Bora , Prashantha Gunaga , Manoranjan Panda , Eldon Scott Priestley , Jeremy Richter
IPC: C07D405/14 , C07D413/14 , C07D417/14 , C07D487/04
CPC classification number: C07D405/14 , C07D413/14 , C07D417/14 , C07D487/04
Abstract: Disclosed are compounds of Formula (I)
or a salt thereof,
wherein R1 is:
each W is independently NR1b or O; Z is a bond or CHR1d; and R1, R2, Rd, R3a, R3b, L1, B, V, Y, and n are defined herein. Also disclosed are methods of using such compounds as inhibitors of ROMK, and pharmaceutical compositions comprising such compounds. These compounds are useful in treating cardiovascular diseases.-
公开(公告)号:US20230167131A1
公开(公告)日:2023-06-01
申请号:US17799028
申请日:2021-02-11
Applicant: BRISTOL-MYERS SQUIBB COMPANY
Inventor: Kumaravel Selvakumar , Venkatram Paidi , Srinivasan Thangathirupathy , Vijaya Kumar Cm , Tirupathi Rao Alajangi , Mallikarjun Reddy Sura , Krishna Mahadevu , Ramesh Kumar Sistla , Piyush Agarwal , Arul Mozhi Subbiah Karuppiah , Jalathi S. Nair , Ooha Morampudi , Manoranjan Panda , Joseph A. Tino , Robert J. Cherney , John V. Duncia , Daniel S. Gardner , T. G. Murali Dhar , Audrey Graham Ross , Paul E. Gormisky , Xiao Zhu , Boris M. Seletsky , Alyssa H. Antropow , Deqiang Niu , Zhengdong Zhu , Guobin Miao , Julio Herman Cuervo
IPC: C07D519/00 , C07D471/04 , C07D487/04 , C07D409/14 , C07D405/14 , C07D413/14
CPC classification number: C07D519/00 , C07D471/04 , C07D487/04 , C07D409/14 , C07D405/14 , C07D413/14
Abstract: The disclosure generally relates to substituted heterocyclic compounds of Formula (Ia), which are inhibitors of PAD4, method for preparing these compounds, pharmaceutical compositions comprising these compounds and use of these compounds in the treatment of a disease or a disorder associated with PAD4 enzyme activity.
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公开(公告)号:US11072626B2
公开(公告)日:2021-07-27
申请号:US16754381
申请日:2018-10-10
Applicant: BRISTOL-MYERS SQUIBB COMPANY
Inventor: Prasada Rao Jalagam , Satheesh Kesavan Nair , Manoranjan Panda , Alicia Regueiro-Ren
IPC: C07H19/056 , C07H19/052 , C07H19/24
Abstract: The present disclosure relates to compounds of formula I, which inhibit Gal-3, and include pharmaceutically acceptable salts, compositions comprising such compounds, and methods using and making such compounds and compositions.
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19.
公开(公告)号:US11014922B2
公开(公告)日:2021-05-25
申请号:US16347849
申请日:2017-11-07
Applicant: BRISTOL-MYERS SQUIBB COMPANY
Inventor: Pratik Devasthale , Fang Moore , Guohua Zhao , Susan Nicole Pieniazek , Kumaravel Selvakumar , Suresh Dhanusu , Manoranjan Panda , Lawrence R. Marcin
IPC: C07D471/04 , A61K31/4375 , A61P1/16 , A61P13/12 , A61P11/00 , A61P35/00
Abstract: The present invention provides compounds of Formula (I): or stereoisomers, tautomers, or pharmaceutically acceptable salts or solvates thereof, wherein all the variables are as defined herein. These compounds are antagonists to αv-containing integrins. This invention also relates to pharmaceutical compositions comprising these compounds and methods of treating a disease, disorder, or condition associated with dysregulation of av-containing integrins, such as pathological fibrosis, transplant rejection, cancer, osteoporosis, and inflammatory disorders, by using the compounds and pharmaceutical compositions.
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公开(公告)号:US10829501B2
公开(公告)日:2020-11-10
申请号:US16739363
申请日:2020-01-10
Applicant: BRISTOL-MYERS SQUIBB COMPANY
Inventor: Leon M. Smith, II , Vladimir Ladziata , Indawati DeLucca , Donald J. P. Pinto , Michael J. Orwat , Andrew K. Dilger , Kumar Balashanmuga Pabbisetty , Wu Yang , Scott A. Shaw , Peter W. Glunz , Manoranjan Panda
IPC: C07D513/04 , C07D213/64 , C07D231/18 , C07D471/04 , C07D471/12 , C07D413/12 , C07D401/12 , C07D231/54 , C07D401/14 , C07D231/12 , A61P15/10 , A61P9/10 , C07D239/06
Abstract: The present invention provides compounds of Formula (I): or stereoisomers, tautomers, or pharmaceutically-acceptable salts thereof, wherein all the variables are as defined herein. These compounds are selective ROCK inhibitors. This invention also relates to pharmaceutical compositions comprising these compounds and methods of treating cardiovascular, smooth muscle, oncologic, neuropathologic, autoimmune, fibrotic, and/or inflammatory disorders using the same.
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