225385-05-7Relevant articles and documents
Heterocyclic compound and preparation method thereof
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Paragraph 0099; 0114; 0115; 0116, (2018/11/03)
The invention discloses a compound shown in the formula (A), or a stereisomer thereof, or medically acceptable salt thereof, or a solvate thereof. The new compound shown in the formula (A) is good inURAT1 inhibitory activity and provides new medical possibilities for clinical treatment of diseases related to abnormal URAT1 activity.
ANTI-INFLAMMATORY COMPOUND HAVING INHIBITORY ACTIVITY AGAINST MULTIPLE TYROSINE KINASES AND PHARMACEUTICAL COMPOSITION CONTAINING SAME
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Paragraph 0281; 0288; 0289, (2013/03/28)
The present invention is for the anti-inflammatory compounds that have an inhibitory activity against protein tyrosine kinases and their pharmaceutical composition(s) containing the compound as the active ingredient. Since the compounds of the present invention can inhibit multiple protein kinases associated with inflammatory diseases and immune disorders, they are useful for their prevention or treatment.
Inhibitors of VEGF receptor and HGF receptor signaling
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Page/Page column 77-78, (2010/11/25)
The invention relates to the inhibition of VEGF receptor signaling and HGF receptor signaling. The invention provides compounds and methods for inhibiting VEGF receptor signaling and HGF receptor signaling. The invention also provides compositions and methods for treating cell proliferative diseases and conditions
INHIBITORS OF VEGF RECEPTOR AND HGF RECEPTOR SIGNALING
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Page/Page column 81, (2010/02/15)
The invention relates to the inhibition of vascular endothelial growth factor (VEGF) receptor signaling and hepatocyte growth factor (HGF) receptor signaling. The invention provides compounds and methods for inhibiting VEGF receptor signaling and HGF receptor signaling. The invention also provides compositions and methods for treating cell proliferative diseases and conditions
Thienopyrimidine and thienopyridine derivatives useful as anticancer agents
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, (2008/06/13)
The invention relates to compounds of the formulas 1 and 2 and to pharmaceutically acceptable salts and hydrates thereof, wherein X1, R1, R2and R11are as defined herein. The invention also relates to pharmaceutical compositions containing the compounds of formulas 1 and 2 and to methods of treating hyperproliferative disorders in a mammal by administering the compounds of formulas 1 and 2.