| Literature DB >> 19447617 |
Róbert Kiss1, Tímea Polgár, Annet Kirabo, Jacqueline Sayyah, Nicholas C Figueroa, Alan F List, Lubomir Sokol, Kenneth S Zuckerman, Meghanath Gali, Kirpal S Bisht, Peter P Sayeski, György M Keseru.
Abstract
Janus kinase 2 (JAK2) plays a crucial role in the pathomechanism of myeloproliferative disorders and hematologic malignancies. A somatic mutation of JAK2 (Val617Phe) was previously shown to occur in 98% of patients with polycythemia vera and 50% of patients with essential thrombocythemia and primary myelofibrosis. Thus, effective JAK2 kinase inhibitors may be of significant therapeutic importance. Here, we applied a structure-based virtual screen to identify novel JAK2 inhibitors. One JAK2 inhibitor in particular, G6, demonstrated remarkable potency as well as specificity, which makes it as a potential lead candidate against diseases related to elevated JAK2 tyrosine kinase activity.Entities:
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Year: 2009 PMID: 19447617 PMCID: PMC2812898 DOI: 10.1016/j.bmcl.2009.04.138
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823