857653-96-4Relevant academic research and scientific papers
IRAK DEGRADERS AND USES THEREOF
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Paragraph 00962; 003285; 003288-003289, (2020/06/19)
The present invention provides compounds, compositions thereof, and methods of using the same.
IRAK DEGRADERS AND USES THEREOF
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Paragraph 00794; 001022; 001025-001026, (2021/01/23)
The present invention provides compounds, compositions thereof, and methods of using the same. The compounds include an IRAK binding moiety and a degradation inducing moiety (DIM). The DIM could be DTM a ligase binding moiety (LBM) or lysine mimetic. The compounds could be useful as IRAK protein kinase inhibitors and applied to IRAK mediated disorders.
GPCR AGONISTS
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Page/Page column 24, (2008/06/13)
Compounds of formula (I): or pharmaceutically acceptable salts thereof, are GPCR agonists and are useful as for the treatment of obesity and diabetes.
GPCR AGONISTS
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Page/Page column 24, (2010/11/25)
Compounds of formula (I): or pharmaceutically acceptable salts thereof, are GPCR agonists and are useful as for the treatment of obesity and diabetes.
G-PROTEIN COUPLED RECEPTOR AGONISTS
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Page/Page column 21-22, (2008/06/13)
Compounds of Formula (I) or pharmaceutically acceptable salts or N-oxides thereof, are agonists of GPR116 and are useful for the treatment of obesity, and for the treatment of diabetes.
HETEROCYCLIC DERIVATIVES AS GPCR RECEPTOR AGONISTS
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Page/Page column 27, (2008/06/13)
Compounds of Formula (I), R1-A-V-B-R2; or pharmaceutically acceptable salts thereof, are agonists of GPR116 and are useful as regulators of satiety, e.g. for the treatment of obesity, and for the treatment of diabetes.
