288252-38-0Relevant academic research and scientific papers
AMIDOPYRIDINE DERIVATIVE, AND USE THEREOF
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Paragraph 0496; 0497; 0501; 0592, (2016/10/08)
The present invention relates to novel amidopyridine derivatives. More specifically, the present invention provides a medicinal agent which is useful as a prophylactic or therapeutic agent for diseases based on the production of cytokines from T cells, comprising as the active ingredient an amidopyridine derivative or a pharmacologically acceptable salt thereof. Provided are an amidopyridine derivative of the following general formula (I): wherein each symbol has the same meaning as defined in the description, or a pharmacologically acceptable salt thereof.
PYRAZOLE COMPOUNDS AS CCR1 ANTAGONISTS
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Page/Page column 61, (2010/01/29)
Disclosed are compounds of the formula I which block the interaction of CCR1 and its ligands and are thus useful for treating a variety of diseases and disorders that are mediated or sustained through the activity of CCR1 including autoimmune diseases, such as rheumatoid arthritis and multiple sclerosis. Also disclosed are pharmaceutical compositions comprising these compounds, methods of using these compounds in the treatment of various diseases and disorders, processes for preparing these compounds and intermediates useful in these processes.
Pyrazole-amides and sulfonamides as sodium channel modulators
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Page/Page column 15, (2010/02/10)
Compounds of the present invention modulate PN3 in mammals and are useful in treating pain in mammals.
Pyrazole-amides and sulfonamides as sodium channel modulators
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, (2010/02/09)
Compounds of the present invention modulate PN3 in mammals and are useful in treating pain in mammals.
AMIDE COMPOUNDS AND MEDICINAL USE THEREOF
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, (2010/01/31)
The present invention relates to a compound of the formula wherein R1 is substituted aryl, heteroaryl and the like, R2 and R3 are hydrogen, alkyl, halogen, hydroxyl group and the like, Q is N, CH and the like, W is hydrogen, alkyl, hydroxycarbonylalkyl and the like, X is halogen, cyano, nitro, amino and the like, X' is hydrogen, halogen, cyano, nitro, and Y is alkyl, hydroxyl group, alkoxy, mercapto and the like and a salt thereof, and a medicine containing the said compound. The compound of the present invention shows a superior inhibitory effect on activated lymphocytes proliferation and is useful as an agent for the prophylaxis or treatment of various autoimmune diseases.
