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Journal Abstract Search

195 related items for PubMed ID: 1695682

  • 1. 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; 33(8):2101-8. PubMed ID: 1695682
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  • 7. Phenylimidazolidin-2-one derivatives as selective 5-HT3 receptor antagonists and refinement of the pharmacophore model for 5-HT3 receptor binding.
    Heidempergher F, Pillan A, Pinciroli V, Vaghi F, Arrigoni C, Bolis G, Caccia C, Dho L, McArthur R, Varasi M.
    J Med Chem; 1997 Oct 10; 40(21):3369-80. PubMed ID: 9341912
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  • 8. Effect of a series of 5-HT4 receptor agonists and antagonists on steroid secretion by the adrenal gland in vitro.
    Contesse V, Hamel C, Delarue C, Lefebvre H, Vaudry H.
    Eur J Pharmacol; 1994 Nov 14; 265(1-2):27-33. PubMed ID: 7883026
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  • 9. 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 14; 7(11):2271-81. PubMed ID: 10632037
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  • 10. Benzoxazines. II. Synthesis, conformational analysis, and structure--activity relationships of 3,4-dihydro-2H-1,4-benzoxazine-8-carboxamide derivatives as potent and long-acting serotonin-3 (5-HT3) receptor antagonists.
    Kuroita T, Marubayashi N, Sano M, Kanzaki K, Inaba K, Kawakita T.
    Chem Pharm Bull (Tokyo); 1996 Nov 14; 44(11):2051-60. PubMed ID: 8945770
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  • 11. Development of high-affinity 5-HT3 receptor antagonists. 2. Two novel tricyclic benzamides.
    Youssefyeh RD, Campbell HF, Airey JE, Klein S, Schnapper M, Powers M, Woodward R, Rodriguez W, Golec S, Studt W.
    J Med Chem; 1992 Mar 06; 35(5):903-11. PubMed ID: 1548679
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  • 15. Novel 5-hydroxytryptamine (5-HT3) receptor antagonists. II. Synthesis and structure-activity relationships of 4,5,6,7-tetrahydro-1H-benzimidazole derivatives.
    Ohta M, Suzuki T, Ohmori J, Koide T, Matsuhisa A, Furuya T, Miyata K, Yanagisawa I.
    Chem Pharm Bull (Tokyo); 1996 May 06; 44(5):1000-8. PubMed ID: 8689715
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  • 16. Evaluation of the receptor selectivity of the H3 receptor antagonists, iodophenpropit and thioperamide: an interaction with the 5-HT3 receptor revealed.
    Leurs R, Tulp MT, Menge WM, Adolfs MJ, Zuiderveld OP, Timmerman H.
    Br J Pharmacol; 1995 Oct 06; 116(4):2315-21. PubMed ID: 8564266
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  • 17. Synthesis and serotonin binding site studies of some conformationally restricted indolylethylamine analogues based on 2-amino-3-(3'-indolyl)bicyclo[2.2.2]octane.
    Schlecht MF, Tsarouhtsis D, Lipovac MN, Debler EA.
    J Med Chem; 1990 Jan 06; 33(1):386-94. PubMed ID: 2136918
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  • 18. 5-HT3 receptor antagonists. 1. New quinoline derivatives.
    Hayashi H, Miwa Y, Miki I, Ichikawa S, Yoda N, Ishii A, Kono M, Suzuki F.
    J Med Chem; 1992 Dec 25; 35(26):4893-902. PubMed ID: 1479589
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  • 19. 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 25; 264(2):654-61. PubMed ID: 8437113
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