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Journal Abstract Search

71 related items for PubMed ID: 23902232

  • 1. 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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  • 2. 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 22; 41(9):1025-40. PubMed ID: 16737760
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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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  • 5. 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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  • 7. Design, synthesis, and biological activity of prazosin-related antagonists. Role of the piperazine and furan units of prazosin on the selectivity for alpha1-adrenoreceptor subtypes.
    Bolognesi ML, Budriesi R, Chiarini A, Poggesi E, Leonardi A, Melchiorre C.
    J Med Chem; 1998 Nov 19; 41(24):4844-53. PubMed ID: 9822553
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  • 9. The affinity and selectivity of α-adrenoceptor antagonists, antidepressants, and antipsychotics for the human α1A, α1B, and α1D-adrenoceptors.
    Proudman RGW, Pupo AS, Baker JG.
    Pharmacol Res Perspect; 2020 Aug 19; 8(4):e00602. PubMed ID: 32608144
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  • 11. Alteration of alpha1-adrenoceptor subtypes in aortas of 12-month-old spontaneously hypertensive rats.
    Xu K, Lu Z, Wei H, Zhang Y, Han C.
    Eur J Pharmacol; 1998 Feb 26; 344(1):31-6. PubMed ID: 9570444
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  • 15. Pharmacological characterization of [3H]-JTH-601, a novel alpha1-adrenoceptor antagonist: binding to recombinant human alpha1-adrenoceptors and human prostates.
    Takahashi M, Taniguchi T, Kanamaru H, Okada K, Muramatsu I.
    Life Sci; 2000 Oct 06; 67(20):2443-51. PubMed ID: 11065167
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  • 16. Isoxazolo-[3,4-d]-pyridazin-7-(6H)-ones and their corresponding 4,5-disubstituted-3-(2H)-pyridazinone analogues as new substrates for alpha1-adrenoceptor selective antagonists: synthesis, modeling, and binding studies.
    Montesano F, Barlocco D, Dal Piaz V, Leonardi A, Poggesi E, Fanelli F, De Benedetti PG.
    Bioorg Med Chem; 1998 Jul 06; 6(7):925-35. PubMed ID: 9730228
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  • 17. Identification of 3,4-dihydro-2H-thiochromene 1,1-dioxide derivatives with a phenoxyethylamine group as highly potent and selective α1D adrenoceptor antagonists.
    Sakauchi N, Furukawa H, Shirai J, Sato A, Kuno H, Saikawa R, Yoshida M.
    Eur J Med Chem; 2017 Oct 20; 139():114-127. PubMed ID: 28800452
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  • 20. New 1,2,3,9-tetrahydro-4H-carbazol-4-one derivatives: analogues of HEAT as ligands for the alpha1-adrenergic receptor subtypes.
    Romeo G, Materia L, Pittalà V, Modica M, Salerno L, Siracusa M, Russo F, Minneman KP.
    Bioorg Med Chem; 2006 Aug 01; 14(15):5211-9. PubMed ID: 16647264
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