164906-64-3Relevant academic research and scientific papers
COMPOUNDS USEFUL IN INHIBITING KETOHEXOKINASE AND METHODS OF MAKING AND USING THE SAME
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Page/Page column 41, (2021/08/20)
The present invention relates to compounds that can act as inhibitors of ketohexokinase (KHK) and that can be useful in the treatment of diseases and/or disorders associated with KHK. In some embodiments, the present invention relates to compounds and com
Discovery of PF-06835919: A Potent Inhibitor of Ketohexokinase (KHK) for the Treatment of Metabolic Disorders Driven by the Overconsumption of Fructose
Futatsugi, Kentaro,Smith, Aaron C.,Tu, Meihua,Raymer, Brian,Ahn, Kay,Coffey, Steven B.,Dowling, Matthew S.,Fernando, Dilinie P.,Gutierrez, Jemy A.,Huard, Kim,Jasti, Jayasankar,Kalgutkar, Amit S.,Knafels, John D.,Pandit, Jayvardhan,Parris, Kevin D.,Perez, Sylvie,Pfefferkorn, Jeffrey A.,Price, David A.,Ryder, Tim,Shavnya, Andre,Stock, Ingrid A.,Tsai, Andy S.,Tesz, Gregory J.,Thuma, Benjamin A.,Weng, Yan,Wisniewska, Hanna M.,Xing, Gang,Zhou, Jun,Magee, Thomas V.
, p. 13546 - 13560 (2021/01/01)
Increased fructose consumption and its subsequent metabolism have been implicated in metabolic disorders such as nonalcoholic fatty liver disease and steatohepatitis (NAFLD/NASH) and insulin resistance. Ketohexokinase (KHK) converts fructose to fructose-1
DISUBSTITUTED PYRAZOLE COMPOUNDS
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Paragraph 0106, (2020/12/25)
The present invention provides a compound of Formula I or a pharmaceutically acceptable salt thereof, and the use of compounds of Formula I for treating metabolic conditions, such as type 2 diabetes mellitus, heart failure, diabetic kidney disease, and no
Substituted Azetidine compounds, their preparation and use as medicaments
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Page/Page column 18, (2008/06/13)
The present invention relates to substituted Azetidine compounds of general formula (I), methods for their preparation, medicaments comprising these compounds as well as their use for the preparation of a medicament for the treatment of humans and animals
7-Azetidinylquinolones as Antibacterial Agents. 3. Synthesis, Properties and Structure-Activity Relationships of the Stereoisomers Containing a 7-(3-Amino-2-methyl-1-azetidinyl) Moiety
Frigola, Jordi,Vano, David,Torrens, Antoni,Gomez-Gomar, Angels,Ortega, Edmundo,Garcia-Granda, Santiago
, p. 1203 - 1215 (2007/10/02)
A series of stereochemically pure 7-(3-amino-2-methyl-1-azetidinyl)-1,4-dihydro-6-fluoro-4-oxoquinoline- and -1,8-naphthyridine-3-carboxylic acids, with varied substituents at the 1-, 5-, and 8-positions, was prepared to determine the effects of chirality
