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PUBMED FOR HANDHELDS

Journal Abstract Search


475 related items for PubMed ID: 29373271

  • 1. Synthesis, biological evaluation and docking study of a new series of di-substituted benzoxazole derivatives as selective COX-2 inhibitors and anti-inflammatory agents.
    Kaur A, Pathak DP, Sharma V, Wakode S.
    Bioorg Med Chem; 2018 Feb 15; 26(4):891-902. PubMed ID: 29373271
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  • 3. Synthesis, Cyclooxygenase-2 Inhibition, Anti-inflammatory Evaluation and Docking Study of Substituted-N-(3,4,5-trimethoxyphenyl)-benzo[d]oxazole Derivatives.
    Kaur A, Wakode S, Pathak DP, Sharma V, Shakya AK.
    Med Chem; 2018 Feb 15; 14(7):660-673. PubMed ID: 29564981
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  • 4. Synthesis and biological evaluation of new nicotinate derivatives as potential anti-inflammatory agents targeting COX-2 enzyme.
    El-Dash Y, Khalil NA, Ahmed EM, Hassan MSA.
    Bioorg Chem; 2021 Feb 15; 107():104610. PubMed ID: 33454504
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  • 5. Synthesis, biological evaluation and docking study of N-(2-(3,4,5-trimethoxybenzyl)benzoxazole-5-yl) benzamide derivatives as selective COX-2 inhibitor and anti-inflammatory agents.
    Kaur A, Pathak DP, Sharma V, Narasimhan B, Sharma P, Mathur R, Wakode S.
    Bioorg Chem; 2018 Dec 15; 81():191-202. PubMed ID: 30138907
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  • 6. 2-Substituted Benzoxazoles as Potent Anti-Inflammatory Agents: Synthesis, Molecular Docking and In vivo Anti-Ulcerogenic Studies.
    Hamid I, Nadeem H, Ansari SF, Khiljee S, Abbasi I, Bukhari A, Arif M, Imran M.
    Med Chem; 2022 Dec 15; 18(7):791-809. PubMed ID: 34931968
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  • 10. Synthesis, cyclooxygenase inhibition, anti-inflammatory evaluation and ulcerogenic liability of novel triarylpyrazoline derivatives as selective COX-2 inhibitors.
    Abdellatif KR, Abdelgawad MA, Labib MB, Zidan TH.
    Bioorg Med Chem Lett; 2015 Dec 15; 25(24):5787-91. PubMed ID: 26546221
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  • 11. Synthesis and biologic evaluation of substituted 5-methyl-2-phenyl-1H-pyrazol-3(2H)-one derivatives as selective COX-2 inhibitors: molecular docking study.
    Dube PN, Bule SS, Mokale SN, Kumbhare MR, Dighe PR, Ushir YV.
    Chem Biol Drug Des; 2014 Oct 15; 84(4):409-19. PubMed ID: 24636540
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  • 12. Synthesis and biological evaluation of pyridazinone derivatives as selective COX-2 inhibitors and potential anti-inflammatory agents.
    Ahmed EM, Kassab AE, El-Malah AA, Hassan MSA.
    Eur J Med Chem; 2019 Jun 01; 171():25-37. PubMed ID: 30904755
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  • 13. Synthesis, anti-inflammatory, ulcerogenic and cyclooxygenase activities of indenopyrimidine derivatives.
    Undare SS, Valekar NJ, Patravale AA, Jamale DK, Vibhute SS, Walekar LS, Kolekar GB, Deshmukh MB, Anbhule PV.
    Bioorg Med Chem Lett; 2016 Feb 01; 26(3):814-818. PubMed ID: 26764192
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  • 15. Design, synthesis, modeling studies and biological evaluation of thiazolidine derivatives containing pyrazole core as potential anti-diabetic PPAR-γ agonists and anti-inflammatory COX-2 selective inhibitors.
    Abdellatif KRA, Fadaly WAA, Kamel GM, Elshaier YAMM, El-Magd MA.
    Bioorg Chem; 2019 Feb 01; 82():86-99. PubMed ID: 30278282
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  • 17. Exploring Anti-inflammatory Potential of Thiazolidinone Derivatives of Benzenesulfonamide via Synthesis, Molecular Docking and Biological Evaluation.
    Bari SB, Firake SD.
    Antiinflamm Antiallergy Agents Med Chem; 2016 Feb 01; 15(1):44-53. PubMed ID: 27216235
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  • 18. Synthesis, anti-inflammatory activity and molecular docking studies of 2,5-diarylfuran amino acid derivatives.
    Stefani HA, Botteselle GV, Zukerman-Schpector J, Caracelli I, da Silva Corrêa D, Farsky SH, Machado ID, Santin JR, Hebeda CB.
    Eur J Med Chem; 2012 Jan 01; 47(1):52-8. PubMed ID: 22071254
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  • 19. Synthesis, biological evaluation, docking study and ulcerogenicity profiling of some novel quinoline-2-carboxamides as dual COXs/LOX inhibitors endowed with anti-inflammatory activity.
    Abdelrahman MH, Youssif BGM, Abdelgawad MA, Abdelazeem AH, Ibrahim HM, Moustafa AEGA, Treamblu L, Bukhari SNA.
    Eur J Med Chem; 2017 Feb 15; 127():972-985. PubMed ID: 27837994
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  • 20. Selective cyclooxygenase inhibition and ulcerogenic liability of some newly prepared anti-inflammatory agents having thiazolo[4,5-d]pyrimidine scaffold.
    Bakr RB, Ghoneim AA, Azouz AA.
    Bioorg Chem; 2019 Jul 15; 88():102964. PubMed ID: 31075742
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