Title of article :
A novel Syk family kinase inhibitor: Design, synthesis, and structure–activity relationship of 1,2,4-triazolo[4,3-c]pyrimidine and 1,2,4-triazolo[1,5-c]pyrimidine derivatives Original Research Article
Author/Authors :
Akihito Hirabayashi، نويسنده , , Harunobu Mukaiyama، نويسنده , , Hiroaki Kobayashi، نويسنده , , Hiroaki Shiohara، نويسنده , , Satoko Nakayama، نويسنده , , Motoyasu Ozawa، نويسنده , , Keiji Miyazawa، نويسنده , , Keiko Misawa، نويسنده , , Hideki Ohnota، نويسنده , , Masayuki Isaji، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2008
Pages :
11
From page :
7347
To page :
7357
Abstract :
Splenic tyrosine kinase (Syk) family kinases, which are members of the protein tyrosine kinase family, play crucial roles in immune responses, with Syk participating in B-cell activation and the zeta-associated protein 70 kDa (ZAP-70) kinase being involved in T-cell activation. Therefore, Syk family kinase inhibitors are candidate therapeutic agents for the treatment of various allergic disorders and autoimmune diseases. We designed 1,2,4-triazolo[4,3-c]pyrimidine and 1,2,4-triazolo[1,5-c]pyrimidine derivatives as Syk family kinase inhibitors, based on literature reports and structure-based drug design. These derivatives showed significant Syk inhibitory activities, with ZAP-70 inhibition. Representative compounds 10d and 11 not only exhibited strong inhibition of both Syk and ZAP-70 kinase but also suppressed IL-2 production by peripheral blood mononuclear cells and whole blood.
Keywords :
Protein tyrosine kinases (PTKs) , Syk , ZAP-70 , Syk and/or ZAP-70 kinase inhibitor
Journal title :
Bioorganic and Medicinal Chemistry
Serial Year :
2008
Journal title :
Bioorganic and Medicinal Chemistry
Record number :
1306783
Link To Document :
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