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
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