Literature DB >> 20144546

Replacement of pyrazol-3-yl amine hinge binder with thiazol-2-yl amine: Discovery of potent and selective JAK2 inhibitors.

Stephanos Ioannidis1, Michelle L Lamb, Lynsie Almeida, Huiping Guan, Bo Peng, Geraldine Bebernitz, Kirsten Bell, Marat Alimzhanov, Michael Zinda.   

Abstract

Thiazol-2-yl amine was identified as an isosteric replacement for pyrazol-3-yl amine during our efforts to identify potent and selective JAK2 inhibitors. The rationale, synthesis and biological evaluation of several analogs is reported, along with the in vivo evaluation of the lead compounds. Copyright 2010 Elsevier Ltd. All rights reserved.

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Year:  2010        PMID: 20144546     DOI: 10.1016/j.bmcl.2010.01.091

Source DB:  PubMed          Journal:  Bioorg Med Chem Lett        ISSN: 0960-894X            Impact factor:   2.823


  2 in total

1.  Design and mechanism of tetrahydrothiophene-based γ-aminobutyric acid aminotransferase inactivators.

Authors:  Hoang V Le; Dustin D Hawker; Rui Wu; Emma Doud; Julia Widom; Ruslan Sanishvili; Dali Liu; Neil L Kelleher; Richard B Silverman
Journal:  J Am Chem Soc       Date:  2015-03-30       Impact factor: 15.419

Review 2.  The recent medicinal chemistry development of Jak2 tyrosine kinase small molecule inhibitors.

Authors:  R Baskin; A Majumder; P P Sayeski
Journal:  Curr Med Chem       Date:  2010       Impact factor: 4.530

  2 in total

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