Literature DB >> 12643942

3,4-Diaryl-5-hydroxyfuranones: highly selective inhibitors of cyclooxygenase-2 with aqueous solubility.

W Cameron Black1, Christine Brideau, Chi Chung Chan, Stella Charleson, Wanda Cromlish, Robert Gordon, Erich L Grimm, Gregory Hughes, Serge Leger, Chun Sing Li, Denis Riendeau, Michel Thérien, Zhaoyin Wang, Li Jing Xu, Petpiboon Prasit.   

Abstract

The introduction of a hydroxyl group into the 5-position of the diaryl furanone system provides highly selective inhibitors of cyclooxygenase-2. These molecules can be converted into their sodium salts which are water soluble, facilitating intravenous formulation. These salts show excellent potency in rat models of pain, fever and inflammation.

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Year:  2003        PMID: 12643942     DOI: 10.1016/s0960-894x(03)00046-5

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


  3 in total

1.  Free energy perturbation approach to the critical assessment of selective cyclooxygenase-2 inhibitors.

Authors:  Hwangseo Park; Sangyoub Lee
Journal:  J Comput Aided Mol Des       Date:  2005-01       Impact factor: 3.686

2.  Cyclooxygenase inhibitors potentiate receptor tyrosine kinase therapies in bladder cancer cells in vitro.

Authors:  Jennifer Bourn; Maria Cekanova
Journal:  Drug Des Devel Ther       Date:  2018-06-13       Impact factor: 4.162

3.  Quinoline based furanones and their nitrogen analogues: Docking, synthesis and biological evaluation.

Authors:  Sukhbir Lal Khokra; Pawan Kaushik; M M Alam; M S Zaman; Aftab Ahmad; Shah Alam Khan; Asif Husain
Journal:  Saudi Pharm J       Date:  2015-06-11       Impact factor: 4.330

  3 in total

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