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Journal Abstract Search

234 related items for PubMed ID: 1613751

  • 1. Novel functional M1 selective muscarinic agonists. Synthesis and structure-activity relationships of 3-(1,2,5-thiadiazolyl)-1,2,5,6-tetrahydro-1-methylpyridines .
    Sauerberg P, Olesen PH, Nielsen S, Treppendahl S, Sheardown MJ, Honoré T, Mitch CH, Ward JS, Pike AJ, Bymaster FP.
    J Med Chem; 1992 Jun 12; 35(12):2274-83. PubMed ID: 1613751
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  • 2. Muscarinic cholinergic agonists and antagonists of the 3-(3-alkyl-1,2,4-oxadiazol-5-yl)-1,2,5,6-tetrahydropyridine type. Synthesis and structure-activity relationships.
    Sauerberg P, Kindtler JW, Nielsen L, Sheardown MJ, Honoré T.
    J Med Chem; 1991 Feb 12; 34(2):687-92. PubMed ID: 1995893
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  • 3. Novel functional M1 selective muscarinic agonists. 2. Synthesis and structure-activity relationships of 3-pyrazinyl-1,2,5,6-tetrahydro-1-methylpyridines. Construction of a molecular model for the M1 pharmacophore.
    Ward JS, Merritt L, Klimkowski VJ, Lamb ML, Mitch CH, Bymaster FP, Sawyer B, Shannon HE, Olesen PH, Honoré T.
    J Med Chem; 1992 Oct 30; 35(22):4011-9. PubMed ID: 1433209
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  • 4. M1 receptor agonist activity is not a requirement for muscarinic antinociception.
    Sheardown MJ, Shannon HE, Swedberg MD, Suzdak PD, Bymaster FP, Olesen PH, Mitch CH, Ward JS, Sauerberg P.
    J Pharmacol Exp Ther; 1997 May 30; 281(2):868-75. PubMed ID: 9152396
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  • 5. Xanomeline: a novel muscarinic receptor agonist with functional selectivity for M1 receptors.
    Shannon HE, Bymaster FP, Calligaro DO, Greenwood B, Mitch CH, Sawyer BD, Ward JS, Wong DT, Olesen PH, Sheardown MJ, Swedberg MD, Suzdak PD, Sauerberg P.
    J Pharmacol Exp Ther; 1994 Apr 30; 269(1):271-81. PubMed ID: 7909557
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  • 7. Muscarinic M1 receptor agonist actions of muscarinic receptor agonists in rabbit vas deferens.
    Shannon HE, Sawyer BD, Bemis KG, Bymaster FP, Health I, Mitch CH, Ward JS.
    Eur J Pharmacol; 1993 Feb 23; 232(1):47-57. PubMed ID: 8458395
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  • 10. New analogues of oxotremorine and oxotremorine-M: estimation of their in vitro affinity and efficacy at muscarinic receptor subtypes.
    Barocelli E, Ballabeni V, Bertoni S, Dallanoce C, De Amici M, De Micheli C, Impicciatore M.
    Life Sci; 2000 Jun 30; 67(6):717-23. PubMed ID: 12659177
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  • 11. Pharmacology of butylthio[2.2.2] (LY297802/NNC11-1053): a novel analgesic with mixed muscarinic receptor agonist and antagonist activity.
    Shannon HE, Sheardown MJ, Bymaster FP, Calligaro DO, Delapp NW, Gidda J, Mitch CH, Sawyer BD, Stengel PW, Ward JS, Wong DT, Olesen PH, Suzdak PD, Sauerberg P, Swedberg MD.
    J Pharmacol Exp Ther; 1997 May 30; 281(2):884-94. PubMed ID: 9152398
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  • 14. Discriminative stimulus properties of the muscarinic receptor agonists Lu 26-046 and O-Me-THPO in rats: evidence for involvement of different muscarinic receptor subtypes.
    Arnt J, Lembøl HL, Meier E, Pedersen H.
    Eur J Pharmacol; 1992 Jul 21; 218(1):159-69. PubMed ID: 1397027
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  • 15. Aliphatic and heterocyclic analogues of arecaidine propargyl ester. Structure-activity relationships of mono- and bivalent ligands at muscarinic M1 (M4), M2 and M3 receptor subtypes.
    Moser U, Gubitz C, Galvan M, Immel-Sehr A, Lambrecht G, Mutshcler E.
    Arzneimittelforschung; 1995 Apr 21; 45(4):449-55. PubMed ID: 7779140
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  • 17. Stereoselective recognition of the enantiomers of phenglutarimide and of six related compounds by four muscarinic receptor subtypes.
    Waelbroeck M, Lazareno S, Pfaff O, Friebe T, Tastenoy M, Mutschler E, Lambrecht G.
    Br J Pharmacol; 1996 Dec 21; 119(7):1319-30. PubMed ID: 8968538
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  • 20. Amide, urea, and carbamate analogues of the muscarinic agent [4-[[N-(3-chlorophenyl)carbamoyl]oxy]-2-butynyl]trimethylammonium chloride.
    Nilsson BM, Vargas HM, Hacksell U.
    J Med Chem; 1992 Jul 24; 35(15):2787-98. PubMed ID: 1379640
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