Literature DB >> 25686006

Progress toward JAK1-selective inhibitors.

Christel J Menet1, Oscar Mammoliti, Miriam López-Ramos.   

Abstract

The discovery of the JAK-STAT pathway was a landmark in cell biology. The identification of these pathways has changed the landscape of treatment of rheumatoid arthritis and other autoimmune diseases. The two first (unselective) JAK inhibitors have recently been approved by the US FDA for the treatment of myelofibrosis and rheumatoid arthritis and many other JAK inhibitors are currently in clinical development or at the discovery stage. Research groups have demonstrated the different roles of JAK member and the therapeutic potential of targeting them selectively. JAK1 plays a critical and potentially dominant role in the transduction of γc cytokine (γc = common γ chain) and in IL-6 signaling. In this review, we will discuss the state-of-the-art research that evokes JAK1 selective inhibition.

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Year:  2015        PMID: 25686006     DOI: 10.4155/fmc.14.149

Source DB:  PubMed          Journal:  Future Med Chem        ISSN: 1756-8919            Impact factor:   3.808


  6 in total

Review 1.  The role of the JAK/STAT signal pathway in rheumatoid arthritis.

Authors:  Charles J Malemud
Journal:  Ther Adv Musculoskelet Dis       Date:  2018-05-19       Impact factor: 5.346

2.  Janus-Associated Kinase 1 (JAK1) Inhibitors as Potential Treatment for Immune Disorders.

Authors:  Ahmed F Abdel-Magid
Journal:  ACS Med Chem Lett       Date:  2017-05-31       Impact factor: 4.345

3.  An Unbiased High-Throughput Screen to Identify Novel Effectors That Impact on Cardiomyocyte Aggregate Levels.

Authors:  Patrick M McLendon; Gregory Davis; James Gulick; Sonia R Singh; Na Xu; Nathan Salomonis; Jeffery D Molkentin; Jeffrey Robbins
Journal:  Circ Res       Date:  2017-06-27       Impact factor: 17.367

4.  Identification of imidazo[1,2-b]pyridazine TYK2 pseudokinase ligands as potent and selective allosteric inhibitors of TYK2 signalling.

Authors:  R Moslin; D Gardner; J Santella; Y Zhang; J V Duncia; C Liu; J Lin; J S Tokarski; J Strnad; D Pedicord; J Chen; Y Blat; A Zupa-Fernandez; L Cheng; H Sun; C Chaudhry; C Huang; C D'Arienzo; J S Sack; J K Muckelbauer; C Chang; J Tredup; D Xie; N Aranibar; J R Burke; P H Carter; D S Weinstein
Journal:  Medchemcomm       Date:  2016-12-15       Impact factor: 3.597

5.  Design, synthesis and evaluation of (R)-3-(7-(methyl(7H-pyrrolo[2,3-d]pyrimidin-4-yl)amino)-5-azaspiro[2.4]heptan-5-yl)-3-oxopropanenitrile as a JAK1-selective inhibitor.

Authors:  Chieyeon Chough; Sunmin Lee; Misuk Joung; Jaemin Lee; Jong Hoon Kim; B Moon Kim
Journal:  Medchemcomm       Date:  2018-01-15       Impact factor: 3.597

6.  Identification of Potent and Selective JAK1 Lead Compounds Through Ligand-Based Drug Design Approaches.

Authors:  Sathya Babu; Santhosh Kumar Nagarajan; Sruthy Sathish; Vir Singh Negi; Honglae Sohn; Thirumurthy Madhavan
Journal:  Front Pharmacol       Date:  2022-04-21       Impact factor: 5.988

  6 in total

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