550377-89-4Relevant academic research and scientific papers
OPIOID RECEPTOR MODULATORS AND PRODUCTS AND METHODS RELATED THERETO
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Page/Page column 215, (2019/10/29)
Compounds are provided having the structure of Formula (I): or a pharmaceutically acceptable isomer, racemate, hydrate, solvate, isotope, or salt thereof, wherein A, B, L, R3, R4, R5, R6, R8, m and n are as defined herein. Such compounds modulate the opioid receptor, particulare the mu-opioid receptor (MOR) and/or the kappa-opioid receptor (KOR), and/or the delta-opioid receptor (DOR). Products containing such compounds, as well as methods for their use and preparation, are also provided.
Novel heterocyclic scaffolds of GW4064 as farnesoid X receptor agonists
Smalley, Terrence L.,Boggs, Sharon,Caravella, Justin A.,Chen, Lihong,Creech, Katrina L.,Deaton, David N.,Kaldor, Istvan,Parks, Derek J.
, p. 280 - 284 (2015/02/19)
The farnesoid X receptor (FXR) may play a crucial role in a number of metabolic diseases and, as such, could potentially serve as a target for the development of therapeutics as a treatment for those diseases. Previous work has described GW4064 as an FXR
NOVEL FXR (NR1H4 ) BINDING AND ACTIVITY MODULATING COMPOUNDS
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, (2011/04/13)
The present invention relates to compounds which bind to the NR1 H4 receptor (FXR) and act as agonists of the NR1 H4 receptor (FXR). The invention further relates to the use of the compounds for the preparation of a medicament for the treatment of diseases and/or conditions through binding of said nuclear receptor by said compounds, and to a process for the synthesis of said compounds.
Novel FXR (NR1H4) binding and activity modulating compounds
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, (2011/04/14)
The present invention relates to compounds which bind to the NR1H4 receptor (FXR) and act as agonists of the NR1H4 receptor (FXR). The invention further relates to the use of the compounds for the preparation of a medicament for the treatment of diseases and/or conditions through binding of said nuclear receptor by said compounds, and to a process for the synthesis of said compounds.
Novel method for synthesizing spiro[4.5]cyclohexadienones through a Pd-catalyzed intramolecular ipso-Friedel-Crafts allylic alkylation of phenols
Nemoto, Tetsuhiro,Ishige, Yuta,Yoshida, Mariko,Kohno, Yuta,Kanematsu, Mutsumi,Hamada, Yasumasa
supporting information; experimental part, p. 5020 - 5023 (2010/12/25)
The first successful Pd-catalyzed intramolecular ipso-Friedel-Crafts allylic alkylation of phenols, which provided a new access to spiro[4.5]cyclohexadienones, is described. The present method could be applied to catalytic enantioselective construction of
FORMAMIDE DERIVATIVES USEFUL AS ADRENOCEPTOR
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Page/Page column 88-89, (2008/06/13)
The invention relates to compounds of formula (1) and to processes for the preparation of, intermediates used in the preparation of, compositions containing and the uses of, such derivatives. The compounds according to the present invention are useful in numerous diseases, disorders and conditions, in particular inflammatory, allergic and respiratory diseases, disorders and conditions.
Sulfonamide derivatives for the treatment of diseases
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Page/Page column 37, (2008/06/13)
The invention relates to compounds of formula (1) and to processes for the preparation of, intermediates used in the preparation of, compositions containing and the uses of, such derivatives. The compounds according to the present invention are useful in
