Literature DB >> 12540232

Hybrid-designed inhibitors of p38 MAP kinase utilizing N-arylpyridazinones.

Steven L Colletti1, Jessica L Frie, Elizabeth C Dixon, Suresh B Singh, Bernard K Choi, Giovanna Scapin, Catherine E Fitzgerald, Sanjeev Kumar, Elizabeth A Nichols, Stephen J O'Keefe, Edward A O'Neill, Gene Porter, Koppara Samuel, Dennis M Schmatz, Cheryl D Schwartz, Wesley L Shoop, Chris M Thompson, James E Thompson, Ruixiu Wang, Andrea Woods, Dennis M Zaller, James B Doherty.   

Abstract

Imidazo[1,2-a]pyridyl N-arylpyridazinones were hybridized from the classic pyridinylimidazoles and the more recent dual hydrogen bond acceptors, resulting in a new structural class of selective p38 MAP kinase inhibitors.

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Year:  2003        PMID: 12540232     DOI: 10.1021/jm025585h

Source DB:  PubMed          Journal:  J Med Chem        ISSN: 0022-2623            Impact factor:   7.446


  4 in total

1.  Metal-free, efficient hydrazination of imidazo[1,2-a]pyridine with diethyl azodicarboxylate in neutral media.

Authors:  Yuanxiang Wang; Brendan Frett; Nick McConnell; Hong-Yu Li
Journal:  Org Biomol Chem       Date:  2015-03-14       Impact factor: 3.876

2.  Efficient access to 2,3-diarylimidazo[1,2-a]pyridines via a one-pot, ligand-free, palladium-catalyzed three-component reaction under microwave irradiation.

Authors:  Yuanxiang Wang; Brendan Frett; Hong-yu Li
Journal:  Org Lett       Date:  2014-05-22       Impact factor: 6.005

3.  CuI nanoparticle-catalyzed synthesis of tetracyclic benzo[e]benzo[4,5]imidazo[1,2-c][1,3]thiazin-6-imine heterocycles by SNAr-type C-S, C-N bond formation from isothiocyanatobenzenes and benzimidazoles.

Authors:  Xiaolong Guo; Luyao Wang; Jing Hu; Mengmeng Zhang
Journal:  RSC Adv       Date:  2018-06-19       Impact factor: 4.036

Review 4.  Recyclization of Maleimides by Binucleophiles as a General Approach for Building Hydrogenated Heterocyclic Systems.

Authors:  Dmitriy Yu Vandyshev; Khidmet S Shikhaliev
Journal:  Molecules       Date:  2022-08-18       Impact factor: 4.927

  4 in total

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