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Journal Abstract Search

234 related items for PubMed ID: 22796043

  • 1. Indole based cyclooxygenase inhibitors: synthesis, biological evaluation, docking and NMR screening.
    Estevão MS, Carvalho LC, Freitas M, Gomes A, Viegas A, Manso J, Erhardt S, Fernandes E, Cabrita EJ, Marques MM.
    Eur J Med Chem; 2012 Aug; 54():823-33. PubMed ID: 22796043
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  • 2. N-1 and C-3 substituted indole Schiff bases as selective COX-2 inhibitors: synthesis and biological evaluation.
    Kaur J, Bhardwaj A, Huang Z, Knaus EE.
    Bioorg Med Chem Lett; 2012 Mar 15; 22(6):2154-9. PubMed ID: 22361134
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  • 3. Synthesis, anti-inflammatory activity and COX-1/COX-2 inhibition of novel substituted cyclic imides. Part 1: Molecular docking study.
    Abdel-Aziz AA, ElTahir KE, Asiri YA.
    Eur J Med Chem; 2011 May 15; 46(5):1648-55. PubMed ID: 21388719
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  • 4. Novel N-substituted indole Schiff bases as dual inhibitors of cyclooxygenase-2 and 5-lipoxygenase enzymes: Synthesis, biological activities in vitro and docking study.
    Lamie PF, Ali WAM, Bazgier V, Rárová L.
    Eur J Med Chem; 2016 Nov 10; 123():803-813. PubMed ID: 27541263
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  • 5. 3-methyl-2-phenyl-1-substituted-indole derivatives as indomethacin analogs: design, synthesis and biological evaluation as potential anti-inflammatory and analgesic agents.
    Abdellatif KR, Lamie PF, Omar HA.
    J Enzyme Inhib Med Chem; 2016 Nov 10; 31(2):318-24. PubMed ID: 25798690
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  • 7. Synthesis and evaluation of dithiolethiones as novel cyclooxygenase inhibitors.
    Zanatta SD, Manallack DT, Jarrott B, Williams SJ.
    Bioorg Med Chem Lett; 2009 Jan 15; 19(2):459-61. PubMed ID: 19056264
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  • 8. Design, synthesis, biological evaluation and docking study of novel indole-2-amide as anti-inflammatory agents with dual inhibition of COX and 5-LOX.
    Huang Y, Zhang B, Li J, Liu H, Zhang Y, Yang Z, Liu W.
    Eur J Med Chem; 2019 Oct 15; 180():41-50. PubMed ID: 31299586
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  • 10. Analogue-based design, synthesis and docking of non-steroidal anti-inflammatory agents. Part 2: methyl sulfanyl/methyl sulfonyl substituted 2,3-diaryl-2,3-dihydro-1H-quinazolin-4-ones.
    Manivannan E, Chaturvedi SC.
    Bioorg Med Chem; 2012 Dec 15; 20(24):7119-27. PubMed ID: 23146282
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  • 15. Isoxazole-Based-Scaffold Inhibitors Targeting Cyclooxygenases (COXs).
    Perrone MG, Vitale P, Panella A, Ferorelli S, Contino M, Lavecchia A, Scilimati A.
    ChemMedChem; 2016 Jun 06; 11(11):1172-87. PubMed ID: 27136372
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  • 18. Synthesis and structure-activity relationship studies of 1,3-diarylprop-2-yn-1-ones: dual inhibitors of cyclooxygenases and lipoxygenases.
    Rao PN, Chen QH, Knaus EE.
    J Med Chem; 2006 Mar 09; 49(5):1668-83. PubMed ID: 16509583
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  • 20. Synthesis and cyclooxygenase inhibitory activities of some N-acylhydrazone derivatives of isoxazolo[4,5-d]pyridazin-4(5H)-ones.
    Unsal-Tan O, Ozden K, Rauk A, Balkan A.
    Eur J Med Chem; 2010 Jun 09; 45(6):2345-52. PubMed ID: 20207453
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