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Journal Abstract Search

201 related items for PubMed ID: 10632037

  • 1. Benzimidazole derivatives. Part 1: Synthesis and structure-activity relationships of new benzimidazole-4-carboxamides and carboxylates as potent and selective 5-HT4 receptor antagonists.
    López-Rodríguez ML, Benhamú B, Viso A, Morcillo MJ, Murcia M, Orensanz L, Alfaro MJ, Martín MI.
    Bioorg Med Chem; 1999 Nov; 7(11):2271-81. PubMed ID: 10632037
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  • 2. 2,3-Dihydro-2-oxo-1H-benzimidazole-1-carboxamides with selective affinity for the 5-HT(4) receptor: synthesis and structure-affinity and structure-activity relationships of a new series of partial agonist and antagonist derivatives.
    Tapia I, Alonso-Cires L, López-Tudanca PL, Mosquera R, Labeaga L, Innerárity A, Orjales A.
    J Med Chem; 1999 Jul 29; 42(15):2870-80. PubMed ID: 10425096
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  • 3. Benzimidazole derivatives. 2. Synthesis and structure-activity relationships of new azabicyclic benzimidazole-4-carboxylic acid derivatives with affinity for serotoninergic 5-HT(3) receptors.
    López-Rodríguez ML, Benhamú B, Morcillo MJ, Tejada ID, Orensanz L, Alfaro MJ, Martín MI.
    J Med Chem; 1999 Dec 02; 42(24):5020-8. PubMed ID: 10585211
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  • 4. Benzimidazole derivatives. 4. The recognition of the voluminous substituent attached to the basic amino group of 5-HT4 receptor antagonists.
    López-Rodríguez ML, Benhamú B, Murcia M, Alvaro E, Campillo M, Pardo L.
    J Comput Aided Mol Des; 2003 Aug 02; 17(8):515-24. PubMed ID: 14703122
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  • 5. Synthesis and structure-activity relationships of potent and orally active 5-HT4 receptor antagonists: indazole and benzimidazolone derivatives.
    Schaus JM, Thompson DC, Bloomquist WE, Susemichel AD, Calligaro DO, Cohen ML.
    J Med Chem; 1998 May 21; 41(11):1943-55. PubMed ID: 9599243
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  • 9. Comparative receptor mapping of serotoninergic 5-HT3 and 5-HT4 binding sites.
    López-Rodríguez ML, Morcillo MJ, Benhamú B, Rosado ML.
    J Comput Aided Mol Des; 1997 Nov 21; 11(6):589-99. PubMed ID: 9491351
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  • 10. (R) and (S) RS 56532: mixed 5-HT3 and 5-HT4 receptor ligands with opposing enantiomeric selectivity.
    Eglen RM, Bonhaus DW, Clark RD, Johnson LG, Lee CH, Leung E, Smith WL, Wong EH, Whiting RL.
    Neuropharmacology; 1994 Nov 21; 33(3-4):515-26. PubMed ID: 7984291
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  • 11. Pharmacological analyses of endo-6-methoxy-8-methyl-8-azabicyclo[3.2.1]oct-3-yl-2,3-dihydro-2-oxo-1 H- benzimidazole-1-carboxylate hydrochloride (DAU 6285) at the 5-hydroxytryptamine4 receptor in the tunica muscularis mucosae of rat esophagus and ileum of guinea pig: role of endogenous 5-hydroxytryptamine.
    Waikar MV, Hegde SS, Ford AP, Clarke DE.
    J Pharmacol Exp Ther; 1993 Feb 21; 264(2):654-61. PubMed ID: 8437113
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  • 12. Synthesis of a new class of 2,3-dihydro-2-oxo-1H-benzimidazole-1-carboxylic acid derivatives as highly potent 5-HT3 receptor antagonists.
    Turconi M, Nicola M, Quintero MG, Maiocchi L, Micheletti R, Giraldo E, Donetti A.
    J Med Chem; 1990 Aug 21; 33(8):2101-8. PubMed ID: 1695682
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  • 17. Arylcarbamate derivatives of 1-piperidineethanol as potent ligands for 5-HT4 receptors.
    Soulier JL, Yang D, Brémont B, Croci T, Guzzi U, Langlois M.
    J Med Chem; 1997 May 23; 40(11):1755-61. PubMed ID: 9171886
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  • 20. Comparison of 5-HT4 receptors in guinea-pig colon and rat oesophagus: effects of novel agonists and antagonists.
    Leung E, Pulido-Rios MT, Bonhaus DW, Pekins LA, Zeitung KD, Hsu SA, Clark RD, Wong EH, Eglen RM.
    Naunyn Schmiedebergs Arch Pharmacol; 1996 Jul 23; 354(2):145-56. PubMed ID: 8857591
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