4.5 Article

Identification of a novel inhibitor of JAK2 tyrosine kinase by structure-based virtual screening

期刊

BIOORGANIC & MEDICINAL CHEMISTRY LETTERS
卷 19, 期 13, 页码 3598-3601

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.bmcl.2009.04.138

关键词

Janus kinase 2; Virtual screening; Inhibitor; Pharmacological evaluation

资金

  1. NHLBI NIH HHS [T32 HL083810, T32 HL083810-03] Funding Source: Medline

向作者/读者索取更多资源

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. (C) 2009 Elsevier Ltd. All rights reserved.

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