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Journal Abstract Search

375 related items for PubMed ID: 23146282

  • 1. 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
    [Abstract] [Full Text] [Related]

  • 2. Analogue-based design, synthesis and molecular docking analysis of 2,3-diaryl quinazolinones as non-ulcerogenic anti-inflammatory agents.
    Manivannan E, Chaturvedi SC.
    Bioorg Med Chem; 2011 Aug 01; 19(15):4520-8. PubMed ID: 21724403
    [Abstract] [Full Text] [Related]

  • 3. Novel click modifiable thioquinazolinones as anti-inflammatory agents: Design, synthesis, biological evaluation and docking study.
    Moussa G, Alaaeddine R, Alaeddine LM, Nassra R, Belal ASF, Ismail A, El-Yazbi AF, Abdel-Ghany YS, Hazzaa A.
    Eur J Med Chem; 2018 Jan 20; 144():635-650. PubMed ID: 29289887
    [Abstract] [Full Text] [Related]

  • 4. 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 20; 46(5):1648-55. PubMed ID: 21388719
    [Abstract] [Full Text] [Related]

  • 5. Synthesis, pharmacological screening and in silico studies of new class of Diclofenac analogues as a promising anti-inflammatory agents.
    Palkar MB, Singhai AS, Ronad PM, Vishwanathswamy AH, Boreddy TS, Veerapur VP, Shaikh MS, Rane RA, Karpoormath R.
    Bioorg Med Chem; 2014 May 15; 22(10):2855-66. PubMed ID: 24751552
    [Abstract] [Full Text] [Related]

  • 6. Design, synthesis, and biological evaluation of 6-substituted-3-(4-methanesulfonylphenyl)-4-phenylpyran-2-ones: a novel class of diarylheterocyclic selective cyclooxygenase-2 inhibitors.
    Praveen Rao PN, Amini M, Li H, Habeeb AG, Knaus EE.
    J Med Chem; 2003 Nov 06; 46(23):4872-82. PubMed ID: 14584938
    [Abstract] [Full Text] [Related]

  • 7. Design and synthesis of quinazolinone derivatives as anti-inflammatory agents: pharmacophore modeling and 3D QSAR studies.
    Chaitanya P, Reddy GD, Varun G, Srikanth LM, Prasad VV, Ravindernath A.
    Med Chem; 2014 Nov 06; 10(7):711-23. PubMed ID: 24286396
    [Abstract] [Full Text] [Related]

  • 8. Dual evaluation of some novel 2-amino-substituted coumarinylthiazoles as anti-inflammatory-antimicrobial agents and their docking studies with COX-1/COX-2 active sites.
    Chandak N, Kumar P, Kaushik P, Varshney P, Sharma C, Kaushik D, Jain S, Aneja KR, Sharma PK.
    J Enzyme Inhib Med Chem; 2014 Aug 06; 29(4):476-84. PubMed ID: 23777557
    [Abstract] [Full Text] [Related]

  • 9. Design, synthesis and evaluation of novel 2-thiophen-5-yl-3H-quinazolin-4-one analogues as inhibitors of transcription factors NF-kappaB and AP-1 mediated transcriptional activation: Their possible utilization as anti-inflammatory and anti-cancer agents.
    Giri RS, Thaker HM, Giordano T, Williams J, Rogers D, Vasu KK, Sudarsanam V.
    Bioorg Med Chem; 2010 Apr 01; 18(7):2796-808. PubMed ID: 20335039
    [Abstract] [Full Text] [Related]

  • 10. Synthesis, biological evaluation and molecular modeling study of pyrazole derivatives as selective COX-2 inhibitors and anti-inflammatory agents.
    Tewari AK, Singh VP, Yadav P, Gupta G, Singh A, Goel RK, Shinde P, Mohan CG.
    Bioorg Chem; 2014 Oct 01; 56():8-15. PubMed ID: 24893208
    [Abstract] [Full Text] [Related]

  • 11. 1,4-Dihydroquinazolin-3(2H)-yl benzamide derivatives as anti-inflammatory and analgesic agents with an improved gastric profile: Design, synthesis, COX-1/2 inhibitory activity and molecular docking study.
    Sakr A, Kothayer H, Ibrahim SM, Baraka MM, Rezq S.
    Bioorg Chem; 2019 Mar 01; 84():76-86. PubMed ID: 30481648
    [Abstract] [Full Text] [Related]

  • 12. Synthesis, anti-inflammatory, analgesic, COX-1/2 inhibitory activities and molecular docking studies of substituted 2-mercapto-4(3H)-quinazolinones.
    Abdel-Aziz AA, Abou-Zeid LA, ElTahir KEH, Ayyad RR, El-Sayed MA, El-Azab AS.
    Eur J Med Chem; 2016 Oct 04; 121():410-421. PubMed ID: 27318118
    [Abstract] [Full Text] [Related]

  • 13. Synthesis and anti-inflammatory activity of some new 4,5-dihydro-1,5-diaryl-1H-pyrazole-3-substituted-heteroazole derivatives.
    Dekhane DV, Pawar SS, Gupta S, Shingare MS, Patil CR, Thore SN.
    Bioorg Med Chem Lett; 2011 Nov 01; 21(21):6527-32. PubMed ID: 21958541
    [Abstract] [Full Text] [Related]

  • 14. Ligand-based design, synthesis and primary in vivo screening of pyrrole derivatives as potential tricyclic anti-inflammatory agents.
    Bijev A, Yaneva D, Bocheva A, Stoev G.
    Arzneimittelforschung; 2006 Nov 01; 56(11):753-9. PubMed ID: 17220053
    [Abstract] [Full Text] [Related]

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  • 16. Synthesis, characterization, evaluation and molecular dynamics studies of 5, 6-diphenyl-1,2,4-triazin-3(2H)-one derivatives bearing 5-substituted 1,3,4-oxadiazole as potential anti-inflammatory and analgesic agents.
    Banerjee AG, Das N, Shengule SA, Srivastava RS, Shrivastava SK.
    Eur J Med Chem; 2015 Aug 28; 101():81-95. PubMed ID: 26117820
    [Abstract] [Full Text] [Related]

  • 17. Synthesis, biological evaluation and docking analysis of 3-methyl-1-phenylchromeno[4,3-c]pyrazol-4(1H)-ones as potential cyclooxygenase-2 (COX-2) inhibitors.
    Grover J, Kumar V, Sobhia ME, Jachak SM.
    Bioorg Med Chem Lett; 2014 Oct 01; 24(19):4638-4642. PubMed ID: 25219899
    [Abstract] [Full Text] [Related]

  • 18. 1,3,4-Trisubstituted pyrazole analogues as promising anti-inflammatory agents.
    Alegaon SG, Alagawadi KR, Garg MK, Dushyant K, Vinod D.
    Bioorg Chem; 2014 Jun 01; 54():51-9. PubMed ID: 24793214
    [Abstract] [Full Text] [Related]

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  • 20. Design and synthesis of novel 4-fluorobenzamide-based derivatives as promising anti-inflammatory and analgesic agents with an enhanced gastric tolerability and COX-inhibitory activity.
    Halim PA, Georgey HH, George MY, El Kerdawy AM, Said MF.
    Bioorg Chem; 2021 Oct 01; 115():105253. PubMed ID: 34390973
    [Abstract] [Full Text] [Related]

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