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PUBMED FOR HANDHELDS

Journal Abstract Search

276 related items for PubMed ID: 19525110

  • 1. Diaminocyclobutenediones as potent and orally bioavailable CXCR2 receptor antagonists: SAR in the phenolic amide region.
    Aki C, Chao J, Ferreira JA, Dwyer MP, Yu Y, Chao J, Merritt RJ, Lai G, Wu M, Hipkin RW, Fan X, Gonsiorek W, Fosseta J, Rindgen D, Fine J, Lundell D, Taveras AG, Biju P.
    Bioorg Med Chem Lett; 2009 Aug 01; 19(15):4446-9. PubMed ID: 19525110
    [Abstract] [Full Text] [Related]

  • 2. Fluoroalkyl alpha side chain containing 3,4-diamino-cyclobutenediones as potent and orally bioavailable CXCR2-CXCR1 dual antagonists.
    Biju P, Taveras AG, Dwyer MP, Yu Y, Chao J, Hipkin RW, Fan X, Rindgen D, Fine J, Lundell D.
    Bioorg Med Chem Lett; 2009 Mar 01; 19(5):1431-3. PubMed ID: 19196511
    [Abstract] [Full Text] [Related]

  • 3. C(4)-alkyl substituted furanyl cyclobutenediones as potent, orally bioavailable CXCR2 and CXCR1 receptor antagonists.
    Chao J, Taveras AG, Chao J, Aki C, Dwyer M, Yu Y, Purakkattle B, Rindgen D, Jakway J, Hipkin W, Fosetta J, Fan X, Lundell D, Fine J, Minnicozzi M, Phillips J, Merritt JR.
    Bioorg Med Chem Lett; 2007 Jul 01; 17(13):3778-83. PubMed ID: 17459706
    [Abstract] [Full Text] [Related]

  • 4. Synthesis and structure-activity relationships of heteroaryl substituted-3,4-diamino-3-cyclobut-3-ene-1,2-dione CXCR2/CXCR1 receptor antagonists.
    Yu Y, Dwyer MP, Chao J, Aki C, Chao J, Purakkattle B, Rindgen D, Bond R, Mayer-Ezel R, Jakway J, Qiu H, Hipkin RW, Fossetta J, Gonsiorek W, Bian H, Fan X, Terminelli C, Fine J, Lundell D, Merritt JR, He Z, Lai G, Wu M, Taveras A.
    Bioorg Med Chem Lett; 2008 Feb 15; 18(4):1318-22. PubMed ID: 18242983
    [Abstract] [Full Text] [Related]

  • 5. Discovery of 2-hydroxy-N,N-dimethyl-3-{2-[[(R)-1-(5- methylfuran-2-yl)propyl]amino]-3,4-dioxocyclobut-1-enylamino}benzamide (SCH 527123): a potent, orally bioavailable CXCR2/CXCR1 receptor antagonist.
    Dwyer MP, Yu Y, Chao J, Aki C, Chao J, Biju P, Girijavallabhan V, Rindgen D, Bond R, Mayer-Ezel R, Jakway J, Hipkin RW, Fossetta J, Gonsiorek W, Bian H, Fan X, Terminelli C, Fine J, Lundell D, Merritt JR, Rokosz LL, Kaiser B, Li G, Wang W, Stauffer T, Ozgur L, Baldwin J, Taveras AG.
    J Med Chem; 2006 Dec 28; 49(26):7603-6. PubMed ID: 17181143
    [Abstract] [Full Text] [Related]

  • 6. Synthesis and structure-activity relationships of new disubstituted phenyl-containing 3,4-diamino-3-cyclobutene-1,2-diones as CXCR2 receptor antagonists.
    Lai G, Merritt JR, He Z, Feng D, Chao J, Czarniecki MF, Rokosz LL, Stauffer TM, Rindgen D, Taveras AG.
    Bioorg Med Chem Lett; 2008 Mar 15; 18(6):1864-8. PubMed ID: 18304809
    [Abstract] [Full Text] [Related]

  • 7. 3,4-Diamino-2,5-thiadiazole-1-oxides as potent CXCR2/CXCR1 antagonists.
    Biju P, Taveras A, Yu Y, Zheng J, Chao J, Rindgen D, Jakway J, Hipkin RW, Fossetta J, Fan X, Fine J, Qiu H, Merritt JR, Baldwin JJ.
    Bioorg Med Chem Lett; 2008 Jan 01; 18(1):228-31. PubMed ID: 18006311
    [Abstract] [Full Text] [Related]

  • 8. Synthesis and structure-activity relationships of 3,4-diaminocyclobut-3-ene-1,2-dione CXCR2 antagonists.
    Merritt JR, Rokosz LL, Nelson KH, Kaiser B, Wang W, Stauffer TM, Ozgur LE, Schilling A, Li G, Baldwin JJ, Taveras AG, Dwyer MP, Chao J.
    Bioorg Med Chem Lett; 2006 Aug 01; 16(15):4107-10. PubMed ID: 16697193
    [Abstract] [Full Text] [Related]

  • 9. 3,4-Diamino-1,2,5-thiadiazole as potent and selective CXCR2 antagonists.
    Biju P, Taveras AG, Yu Y, Zheng J, Hipkin RW, Fossetta J, Fan X, Fine J, Lundell D.
    Bioorg Med Chem Lett; 2009 Mar 01; 19(5):1434-7. PubMed ID: 19200721
    [Abstract] [Full Text] [Related]

  • 10. Pharmacological characterization of Sch527123, a potent allosteric CXCR1/CXCR2 antagonist.
    Gonsiorek W, Fan X, Hesk D, Fossetta J, Qiu H, Jakway J, Billah M, Dwyer M, Chao J, Deno G, Taveras A, Lundell DJ, Hipkin RW.
    J Pharmacol Exp Ther; 2007 Aug 01; 322(2):477-85. PubMed ID: 17496166
    [Abstract] [Full Text] [Related]

  • 11. N,N'-Diarylcyanoguanidines as antagonists of the CXCR2 and CXCR1 chemokine receptors.
    Nie H, Widdowson KL, Palovich MR, Fu W, Elliott JD, Bryan DL, Burman M, Schmidt DB, Foley JJ, Sarau HM, Busch-Petersen J.
    Bioorg Med Chem Lett; 2006 Nov 01; 16(21):5513-6. PubMed ID: 16934456
    [Abstract] [Full Text] [Related]

  • 12. Bradykinin B1 antagonists: biphenyl SAR studies in the cyclopropanecarboxamide series.
    Kuduk SD, DiPardo RM, Chang RK, Di Marco CN, Murphy KL, Ransom RW, Reiss DR, Tang C, Prueksaritanont T, Pettibone DJ, Bock MG.
    Bioorg Med Chem Lett; 2007 Jul 01; 17(13):3608-12. PubMed ID: 17482459
    [Abstract] [Full Text] [Related]

  • 13. Hit-to-Lead studies: the discovery of potent, orally bioavailable thiazolopyrimidine CXCR2 receptor antagonists.
    Baxter A, Cooper A, Kinchin E, Moakes K, Unitt J, Wallace A.
    Bioorg Med Chem Lett; 2006 Feb 15; 16(4):960-3. PubMed ID: 16297626
    [Abstract] [Full Text] [Related]

  • 14. Design of noncompetitive interleukin-8 inhibitors acting on CXCR1 and CXCR2.
    Moriconi A, Cesta MC, Cervellera MN, Aramini A, Coniglio S, Colagioia S, Beccari AR, Bizzarri C, Cavicchia MR, Locati M, Galliera E, Di Benedetto P, Vigilante P, Bertini R, Allegretti M.
    J Med Chem; 2007 Aug 23; 50(17):3984-4002. PubMed ID: 17665889
    [Abstract] [Full Text] [Related]

  • 15. Discovery of potent and orally bioavailable N,N'-diarylurea antagonists for the CXCR2 chemokine receptor.
    Jin Q, Nie H, McCleland BW, Widdowson KL, Palovich MR, Elliott JD, Goodman RM, Burman M, Sarau HM, Ward KW, Nord M, Orr BM, Gorycki PD, Busch-Petersen J.
    Bioorg Med Chem Lett; 2004 Sep 06; 14(17):4375-8. PubMed ID: 15357956
    [Abstract] [Full Text] [Related]

  • 16. Discovery of novel aminothiadiazole amides as selective EP(3) receptor antagonists.
    Hilfiker MA, Wang N, Hou X, Du Z, Pullen MA, Nord M, Nagilla R, Fries HE, Wu CW, Sulpizio AC, Jaworski JP, Morrow D, Edwards RM, Jin J.
    Bioorg Med Chem Lett; 2009 Aug 01; 19(15):4292-5. PubMed ID: 19487124
    [Abstract] [Full Text] [Related]

  • 17. Comparison of N,N'-diarylsquaramides and N,N'-diarylureas as antagonists of the CXCR2 chemokine receptor.
    McCleland BW, Davis RS, Palovich MR, Widdowson KL, Werner ML, Burman M, Foley JJ, Schmidt DB, Sarau HM, Rogers M, Salyers KL, Gorycki PD, Roethke TJ, Stelman GJ, Azzarano LM, Ward KW, Busch-Petersen J.
    Bioorg Med Chem Lett; 2007 Mar 15; 17(6):1713-7. PubMed ID: 17236763
    [Abstract] [Full Text] [Related]

  • 18. Evaluation of potent and selective small-molecule antagonists for the CXCR2 chemokine receptor.
    Widdowson KL, Elliott JD, Veber DF, Nie H, Rutledge MC, McCleland BW, Xiang JN, Jurewicz AJ, Hertzberg RP, Foley JJ, Griswold DE, Martin L, Lee JM, White JR, Sarau HM.
    J Med Chem; 2004 Mar 11; 47(6):1319-21. PubMed ID: 14998320
    [Abstract] [Full Text] [Related]

  • 19. Development of a systemically-active dual CXCR1/CXCR2 allosteric inhibitor and its efficacy in a model of transient cerebral ischemia in the rat.
    Garau A, Bertini R, Mosca M, Bizzarri C, Anacardio R, Triulzi S, Allegretti M, Ghezzi P, Villa P.
    Eur Cytokine Netw; 2006 Mar 11; 17(1):35-41. PubMed ID: 16613761
    [Abstract] [Full Text] [Related]

  • 20. Small, non-peptide C5a receptor antagonists: part 2.
    Blagg J, Mowbray C, Pryde D, Salmon G, Fairman D, Schmid E, Beaumont K.
    Bioorg Med Chem Lett; 2008 Oct 15; 18(20):5605-8. PubMed ID: 18804369
    [Abstract] [Full Text] [Related]

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