Literature DB >> 12630292

Protein kinase inhibitors from the urea class.

Jacques Dumas1.   

Abstract

Protein kinase inhibitors hold great potential as novel therapies for cancer and inflammatory disorders. While bis-aryl ureas have been reported as kinase inhibitors as early as 1996, a number of publications and patent applications appeared in the literature during the past two years. Three urea-based kinase inhibitors are currently undergoing clinical trials. The present review summarizes available data, and provides an overview of the structure-activity relationships against a variety of kinase targets, including p38, Raf-1 and cyclin-dependent kinases.

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Year:  2002        PMID: 12630292

Source DB:  PubMed          Journal:  Curr Opin Drug Discov Devel        ISSN: 1367-6733


  8 in total

1.  A new synthesis of imidazolidin-2-ones via Pd-catalyzed carboamination of N-allylureas.

Authors:  Jonathan A Fritz; Josephine S Nakhla; John P Wolfe
Journal:  Org Lett       Date:  2006-06-08       Impact factor: 6.005

2.  Palladium-Catalyzed Carboetherification and Carboamination Reactions of γ-Hydroxy- and γ-Aminoalkenes for the Synthesis of Tetrahydrofurans and Pyrrolidines.

Authors:  John P Wolfe
Journal:  European J Org Chem       Date:  2007-02

3.  Synthesis of enantiomerically enriched imidazolidin-2-ones through asymmetric palladium-catalyzed alkene carboamination reactions.

Authors:  Brett A Hopkins; John P Wolfe
Journal:  Angew Chem Int Ed Engl       Date:  2012-08-31       Impact factor: 15.336

Review 4.  Melanoma genetics and the development of rational therapeutics.

Authors:  Yakov Chudnovsky; Paul A Khavari; Amy E Adams
Journal:  J Clin Invest       Date:  2005-04       Impact factor: 14.808

5.  Synthetic studies toward aryl-(4-aryl-4H-[1,2,4]triazole-3-yl)-amine from 1,3-diarylthiourea as urea mimetics.

Authors:  Amarnath Natarajan; Yuhong Guo; Haribabu Arthanari; Gerhard Wagner; Jose A Halperin; Michael Chorev
Journal:  J Org Chem       Date:  2005-08-05       Impact factor: 4.354

6.  Antileukemic Effects of Novel First- and Second-Generation FLT3 Inhibitors: Structure-Affinity Comparison.

Authors:  Ellen Weisberg; Johannes Roesel; Pascal Furet; Guido Bold; Patricia Imbach; Andreas Flörsheimer; Georgio Caravatti; Jingrui Jiang; Paul Manley; Arghya Ray; James D Griffin
Journal:  Genes Cancer       Date:  2010-10

7.  Applying ligands profiling using multiple extended electron distribution based field templates and feature trees similarity searching in the discovery of new generation of urea-based antineoplastic kinase inhibitors.

Authors:  Eman M Dokla; Amr H Mahmoud; Mohamed S A Elsayed; Ahmed H El-Khatib; Michael W Linscheid; Khaled A Abouzid
Journal:  PLoS One       Date:  2012-11-20       Impact factor: 3.240

8.  Synthesis and In Vitro Antiproliferative Activity of New 1-Phenyl-3-(4-(pyridin-3-yl)phenyl)urea Scaffold-Based Compounds.

Authors:  Mohammad M Al-Sanea; Mohammed Safwan Ali Khan; Ahmed Z Abdelazem; So Ha Lee; Pooi Ling Mok; Mohammed Gamal; Mohamed E Shaker; Muhammad Afzal; Bahaa G M Youssif; Nesreen Nabil Omar
Journal:  Molecules       Date:  2018-01-31       Impact factor: 4.411

  8 in total

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