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Journal Abstract Search

152 related items for PubMed ID: 8382766

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  • 2. SDZ ENS 163 is a selective M1 agonist and induces release of acetylcholine.
    Enz A, Shapiro G, Supavilai P, Boddeke HW.
    Naunyn Schmiedebergs Arch Pharmacol; 1992 Mar; 345(3):282-7. PubMed ID: 1620233
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  • 3. L-689,660, a novel cholinomimetic with functional selectivity for M1 and M3 muscarinic receptors.
    Hargreaves RJ, McKnight AT, Scholey K, Newberry NR, Street LJ, Hutson PH, Semark JE, Harley EA, Patel S, Freedman SB.
    Br J Pharmacol; 1992 Oct; 107(2):494-501. PubMed ID: 1422595
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  • 4. 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; 119(7):1319-30. PubMed ID: 8968538
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  • 9. Effects of agonist efficacy on desensitization of phosphoinositide hydrolysis mediated by m1 and m3 muscarinic receptors expressed in Chinese hamster ovary cells.
    Hu J, Wang SZ, el-Fakahany EE.
    J Pharmacol Exp Ther; 1991 Jun; 257(3):938-45. PubMed ID: 1710663
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  • 10. Pharmacological differentiation of presynaptic M1 muscarinic receptors modulating acetylcholine release from postsynaptic muscarinic receptors in guinea-pig ileum.
    Kawashima K, Fujimoto K, Suzuki T, Oohata H.
    Gen Pharmacol; 1990 Jun; 21(1):17-21. PubMed ID: 2298386
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  • 11. Positive cooperativity of acetylcholine and other agonists with allosteric ligands on muscarinic acetylcholine receptors.
    Jakubík J, Bacáková L, El-Fakahany EE, Tucek S.
    Mol Pharmacol; 1997 Jul; 52(1):172-9. PubMed ID: 9224827
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  • 15. Pharmacological properties of cloned muscarinic receptors expressed in A9 L cells; comparison with in vitro models.
    Boddeke HW, Buttini M.
    Eur J Pharmacol; 1991 Sep 17; 202(2):151-7. PubMed ID: 1802743
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  • 16. The pharmacological assessment of RS 86 (2-ethyl-8-methyl-2,8-diazaspiro-[4,5]-decan-1,3-dion hydrobromide). A potent, specific muscarinic acetylcholine receptor agonist.
    Palacios JM, Bolliger G, Closse A, Enz A, Gmelin G, Malanowski J.
    Eur J Pharmacol; 1986 Jun 05; 125(1):45-62. PubMed ID: 3732391
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  • 18. Distinct kinetic binding properties of N-[3H]-methylscopolamine afford differential labeling and localization of M1, M2, and M3 muscarinic receptor subtypes in primate brain.
    Flynn DD, Mash DC.
    Synapse; 1993 Aug 05; 14(4):283-96. PubMed ID: 8248852
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  • 19. Activation of cerebral function by CS-932, a functionally selective M1 partial agonist: neurochemical characterization and pharmacological studies.
    Iwata N, Kozuka M, Hara T, Kanek T, Tonohiro T, Sugimoto M, Niitsu Y, Kondo Y, Yamamoto T, Sakai J, Nagano M.
    Jpn J Pharmacol; 2000 Nov 05; 84(3):266-80. PubMed ID: 11138727
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