Literature DB >> 20205617

Recent developments on JAK2 inhibitors: a patent review.

Róbert Kiss1, Peter P Sayeski, György M Keserũ.   

Abstract

IMPORTANCE OF THE FIELD: JAK2 is one of the most promising targets against neoplastic growth. A somatic mutation (V617F) resulting in enhanced JAK2 kinase activity can be frequently found in patients with serious myeloproliferative neoplasms such as polycythemia vera, essential thrombocythemia and primary myelofibrosis. Preclinical results strongly support that JAK2 inhibitors could be effectively used in these indications. Pharmaceutical companies and academic groups have developed a number of potent JAK2 inhibitors during the last decade. Tolerability and effectiveness of the most promising compounds are currently being investigated in clinical trials. AREAS COVERED IN THIS REVIEW: In this paper, we aim to give a comprehensive review of the currently available patent literature of JAK2 inhibitors. WHAT THE READER WILL GAIN: We tried to collect the published core structures possessing JAK2 inhibitory potency including compounds developed by academic and industrial research groups. We review the currently available patent literature as well as the key papers containing additional information about the described JAK2 inhibitors. Clinical status data were collected by searching the Prous Integrity and Pharmaprojects databases. TAKE HOME MESSAGE: The significant number of JAK2 inhibitors published and numerous clinical trials involving these compounds suggest that some of them might be approved in the next few years and can serve as novel drugs for the treatment of JAK2-dependent pathologies.

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Year:  2010        PMID: 20205617     DOI: 10.1517/13543771003639436

Source DB:  PubMed          Journal:  Expert Opin Ther Pat        ISSN: 1354-3776            Impact factor:   6.674


  7 in total

1.  Jak/STAT pathways in cytokine signaling and myeloproliferative disorders: approaches for targeted therapies.

Authors:  Shashidhar S Jatiani; Stacey J Baker; Lewis R Silverman; E Premkumar Reddy
Journal:  Genes Cancer       Date:  2010-10

2.  Identification of novel SAR properties of the Jak2 small molecule inhibitor G6: significance of the para-hydroxyl orientation.

Authors:  Rebekah Baskin; Meghanath Gali; Sung O Park; Zhizhuang Joe Zhao; György M Keseru; Kirpal S Bisht; Peter P Sayeski
Journal:  Bioorg Med Chem Lett       Date:  2011-12-21       Impact factor: 2.823

3.  The constitutive activation of Jak2-V617F is mediated by a π stacking mechanism involving phenylalanines 595 and 617.

Authors:  Kavitha Gnanasambandan; Andrew Magis; Peter P Sayeski
Journal:  Biochemistry       Date:  2010-10-29       Impact factor: 3.162

4.  A computationally affordable approach for accurate prediction of the binding affinity of JAK2 inhibitors.

Authors:  Nguyen Thi Mai; Ngo Thi Lan; Thien Y Vu; Nguyen Thanh Tung; Huong Thi Thu Phung
Journal:  J Mol Model       Date:  2022-05-23       Impact factor: 1.810

5.  Genetic resistance to JAK2 enzymatic inhibitors is overcome by HSP90 inhibition.

Authors:  Oliver Weigert; Andrew A Lane; Liat Bird; Nadja Kopp; Bjoern Chapuy; Diederik van Bodegom; Angela V Toms; Sachie Marubayashi; Amanda L Christie; Michael McKeown; Ronald M Paranal; James E Bradner; Akinori Yoda; Christoph Gaul; Eric Vangrevelinghe; Vincent Romanet; Masato Murakami; Ralph Tiedt; Nicolas Ebel; Emeline Evrot; Alain De Pover; Catherine H Régnier; Dirk Erdmann; Francesco Hofmann; Michael J Eck; Stephen E Sallan; Ross L Levine; Andrew L Kung; Fabienne Baffert; Thomas Radimerski; David M Weinstock
Journal:  J Exp Med       Date:  2012-01-23       Impact factor: 14.307

6.  Design, Synthesis and Docking Studies of Flavokawain B Type Chalcones and Their Cytotoxic Effects on MCF-7 and MDA-MB-231 Cell Lines.

Authors:  Addila Abu Bakar; Muhammad Nadeem Akhtar; Norlaily Mohd Ali; Swee Keong Yeap; Ching Kheng Quah; Wan-Sin Loh; Noorjahan Banu Alitheen; Seema Zareen; Zaheer Ul-Haq; Syed Adnan Ali Shah
Journal:  Molecules       Date:  2018-03-08       Impact factor: 4.411

7.  Discovery of New Apoptosis-Inducing Agents for Breast Cancer Based on Ethyl 2-Amino-4,5,6,7-Tetra Hydrobenzo[b]Thiophene-3-Carboxylate: Synthesis, In Vitro, and In Vivo Activity Evaluation.

Authors:  Emad M Gad; Mohamed S Nafie; Elsayed H Eltamany; Magdy S A G Hammad; Assem Barakat; Ahmed T A Boraei
Journal:  Molecules       Date:  2020-05-28       Impact factor: 4.411

  7 in total

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