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PUBMED FOR HANDHELDS

Journal Abstract Search


123 related items for PubMed ID: 19375913

  • 1. Triazinediones as prokineticin 1 receptor antagonists. Part 1: SAR, synthesis and biological evaluation.
    Ralbovsky JL, Lisko JG, Palmer JM, Mabus J, Chevalier KM, Schulz MJ, Dyatkin AB, Miskowski TA, Coats SJ, Hornby P, He W.
    Bioorg Med Chem Lett; 2009 May 15; 19(10):2661-3. PubMed ID: 19375913
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  • 2. Triazine compounds as antagonists at Bv8-prokineticin receptors.
    Balboni G, Lazzari I, Trapella C, Negri L, Lattanzi R, Giannini E, Nicotra A, Melchiorri P, Visentin S, Nuccio CD, Salvadori S.
    J Med Chem; 2008 Dec 11; 51(23):7635-9. PubMed ID: 19006379
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  • 3. A new convenient synthetic method and preliminary pharmacological characterization of triazinediones as prokineticin receptor antagonists.
    Congiu C, Onnis V, Deplano A, Salvadori S, Marconi V, Maftei D, Negri L, Lattanzi R, Balboni G.
    Eur J Med Chem; 2014 Jun 23; 81():334-40. PubMed ID: 24852280
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  • 4. Structure-activity relationships of 1,3,5-triazine-2,4,6-triones as human gonadotropin-releasing hormone receptor antagonists.
    Guo Z, Wu D, Zhu YF, Tucci FC, Regan CF, Rowbottom MW, Struthers RS, Xie Q, Reijmers S, Sullivan SK, Sai Y, Chen C.
    Bioorg Med Chem Lett; 2005 Aug 15; 15(16):3685-90. PubMed ID: 15951171
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  • 6. Phenylpiperidine-benzoxazinones as urotensin-II receptor antagonists: synthesis, SAR, and in vivo assessment.
    Luci DK, Ghosh S, Smith CE, Qi J, Wang Y, Haertlein B, Parry TJ, Li J, Almond HR, Minor LK, Damiano BP, Kinney WA, Maryanoff BE, Lawson EC.
    Bioorg Med Chem Lett; 2007 Dec 01; 17(23):6489-92. PubMed ID: 17933531
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  • 8. Synthesis and SAR of 1,2,3,4-tetrahydroisoquinolin-1-ones as novel G-protein-coupled receptor 40 (GPR40) antagonists.
    Humphries PS, Benbow JW, Bonin PD, Boyer D, Doran SD, Frisbie RK, Piotrowski DW, Balan G, Bechle BM, Conn EL, Dirico KJ, Oliver RM, Soeller WC, Southers JA, Yang X.
    Bioorg Med Chem Lett; 2009 May 01; 19(9):2400-3. PubMed ID: 19346127
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  • 10. Synthesis and structure-activity relationships of 8-(pyrid-3-yl)pyrazolo[1,5-a]-1,3,5-triazines: potent, orally bioavailable corticotropin releasing factor receptor-1 (CRF1) antagonists.
    Gilligan PJ, Clarke T, He L, Lelas S, Li YW, Heman K, Fitzgerald L, Miller K, Zhang G, Marshall A, Krause C, McElroy JF, Ward K, Zeller K, Wong H, Bai S, Saye J, Grossman S, Zaczek R, Arneric SP, Hartig P, Robertson D, Trainor G.
    J Med Chem; 2009 May 14; 52(9):3084-92. PubMed ID: 19361209
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  • 13. Development of potent and selective small-molecule human Urotensin-II antagonists.
    McAtee JJ, Dodson JW, Dowdell SE, Girard GR, Goodman KB, Hilfiker MA, Sehon CA, Sha D, Wang GZ, Wang N, Viet AQ, Zhang D, Aiyar NV, Behm DJ, Carballo LH, Evans CA, Fries HE, Nagilla R, Roethke TJ, Xu X, Yuan CC, Douglas SA, Neeb MJ.
    Bioorg Med Chem Lett; 2008 Jun 15; 18(12):3500-3. PubMed ID: 18502123
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  • 14. Discovery of imidazo[1,2-b][1,2,4]triazines as GABA(A) alpha2/3 subtype selective agonists for the treatment of anxiety.
    Russell MG, Carling RW, Street LJ, Hallett DJ, Goodacre S, Mezzogori E, Reader M, Cook SM, Bromidge FA, Newman R, Smith AJ, Wafford KA, Marshall GR, Reynolds DS, Dias R, Ferris P, Stanley J, Lincoln R, Tye SJ, Sheppard WF, Sohal B, Pike A, Dominguez M, Atack JR, Castro JL.
    J Med Chem; 2006 Feb 23; 49(4):1235-8. PubMed ID: 16480260
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  • 15. (2-Arylethenyl)-1,3,5-triazin-2-amines as a novel histamine H4 receptor ligands.
    Kamińska K, Ziemba J, Ner J, Schwed JS, Łażewska D, Więcek M, Karcz T, Olejarz A, Latacz G, Kuder K, Kottke T, Zygmunt M, Sapa J, Karolak-Wojciechowska J, Stark H, Kieć-Kononowicz K.
    Eur J Med Chem; 2015 Oct 20; 103():238-51. PubMed ID: 26360048
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  • 20. N-Glycine-sulfonamides as potent dual orexin 1/orexin 2 receptor antagonists.
    Aissaoui H, Koberstein R, Zumbrunn C, Gatfield J, Brisbare-Roch C, Jenck F, Treiber A, Boss C.
    Bioorg Med Chem Lett; 2008 Nov 01; 18(21):5729-33. PubMed ID: 18845436
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