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Journal Abstract Search

121 related items for PubMed ID: 16737760

  • 1. QSAR study for a novel series of ortho disubstituted phenoxy analogues of alpha1-adrenoceptor antagonist WB4101.
    Pallavicini M, Fumagalli L, Gobbi M, Bolchi C, Colleoni S, Moroni B, Pedretti A, Rusconi C, Vistoli G, Valoti E.
    Eur J Med Chem; 2006 Sep; 41(9):1025-40. PubMed ID: 16737760
    [Abstract] [Full Text] [Related]

  • 2. QSAR study for a novel series of ortho monosubstituted phenoxy analogues of alpha1-adrenoceptor antagonist WB4101.
    Fumagalli L, Bolchi C, Colleoni S, Gobbi M, Moroni B, Pallavicini M, Pedretti A, Villa L, Vistoli G, Valoti E.
    Bioorg Med Chem; 2005 Apr 01; 13(7):2547-59. PubMed ID: 15755656
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  • 3. WB4101-related compounds: new, subtype-selective alpha1-adrenoreceptor antagonists (or inverse agonists?).
    Pallavicini M, Budriesi R, Fumagalli L, Ioan P, Chiarini A, Bolchi C, Ugenti MP, Colleoni S, Gobbi M, Valoti E.
    J Med Chem; 2006 Nov 30; 49(24):7140-9. PubMed ID: 17125266
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  • 4. 6-methoxy-7-benzofuranoxy and 6-methoxy-7-indolyloxy analogues of 2-[2-(2,6-Dimethoxyphenoxy)ethyl]aminomethyl-1,4-benzodioxane (WB4101):1 discovery of a potent and selective α1D-adrenoceptor antagonist.
    Fumagalli L, Pallavicini M, Budriesi R, Bolchi C, Canovi M, Chiarini A, Chiodini G, Gobbi M, Laurino P, Micucci M, Straniero V, Valoti E.
    J Med Chem; 2013 Aug 22; 56(16):6402-12. PubMed ID: 23902232
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  • 5. Structure-affinity studies for a novel series of homochiral naphtho and tetrahydronaphtho analogues of alpha 1 antagonist WB-4101.
    Bolchi C, Catalano P, Fumagalli L, Gobbi M, Pallavicini M, Pedretti A, Villa L, Vistoli G, Valoti E.
    Bioorg Med Chem; 2004 Sep 15; 12(18):4937-51. PubMed ID: 15336273
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  • 6. Structure-activity relationships in 1,4-benzodioxan-related compounds. 8.(1) {2-[2-(4-chlorobenzyloxy)phenoxy]ethyl}-[2-(2,6-dimethoxyphenoxy)ethyl]amine (clopenphendioxan) as a tool to highlight the involvement of alpha1D- and alpha1B-adrenoreceptor subtypes in the regulation of human PC-3 prostate cancer cell apoptosis and proliferation.
    Quaglia W, Santoni G, Pigini M, Piergentili A, Gentili F, Buccioni M, Mosca M, Lucciarini R, Amantini C, Nabissi MI, Ballarini P, Poggesi E, Leonardi A, Giannella M.
    J Med Chem; 2005 Dec 01; 48(24):7750-63. PubMed ID: 16302814
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  • 11. Novel adrenoceptor antagonists with a tricyclic pyrrolodipyridazine skeleton.
    Barlocco D, Cignarella G, Montesano F, Leonardi A, Mella M, Toma L.
    J Med Chem; 1999 Jan 14; 42(1):173-7. PubMed ID: 9888842
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  • 12. Synthesis and α1-adrenoceptor antagonist activity of tamsulosin analogues.
    Sagratini G, Angeli P, Buccioni M, Gulini U, Marucci G, Melchiorre C, Poggesi E, Giardinà D.
    Eur J Med Chem; 2010 Dec 14; 45(12):5800-7. PubMed ID: 20934789
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  • 14. Synthesis, pharmacological evaluation, and structure-activity relationship and quantitative structure-activity relationship studies on novel derivatives of 2,4-diamino-6,7-dimethoxyquinazoline alpha1-adrenoceptor antagonists.
    Leonardi A, Motta G, Boi C, Testa R, Poggesi E, De Benedetti PG, Menziani MC.
    J Med Chem; 1999 Feb 11; 42(3):427-37. PubMed ID: 9986714
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  • 15. CoMFA methodology in structure-activity analysis of hexahydro- and octahydropyrido[1,2-c]pyrimidine derivatives based on affinity towards 5-HT1A, 5-HT2A and alpha1-adrenergic receptors.
    Maciejewska D, Zołek T, Herold F.
    J Mol Graph Model; 2006 Nov 11; 25(3):353-62. PubMed ID: 16542863
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