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Journal Abstract Search

183 related items for PubMed ID: 8355199

  • 1. 4-morpholinecarboximidine-N-1-adamantyl-N'-cyclohexylhydrochloride (U-37883A): pharmacological characterization of a novel antagonist of vascular ATP-sensitive K+ channel openers.
    Meisheri KD, Humphrey SJ, Khan SA, Cipkus-Dubray LA, Smith MP, Jones AW.
    J Pharmacol Exp Ther; 1993 Aug; 266(2):655-65. PubMed ID: 8355199
    [Abstract] [Full Text] [Related]

  • 2. Synergistic effects of glyburide and U-37883A, two structurally different vascular ATP-sensitive potassium channel antagonists.
    Ohrnberger CE, Khan SA, Meisheri KD.
    J Pharmacol Exp Ther; 1993 Oct; 267(1):25-30. PubMed ID: 8229751
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  • 3. Inhibition of vascular K(ATP) channels by U-37883A: a comparison with cardiac and skeletal muscle.
    Wellman GC, Barrett-Jolley R, Köppel H, Everitt D, Quayle JM.
    Br J Pharmacol; 1999 Oct; 128(4):909-16. PubMed ID: 10556925
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  • 4. Vascular pharmacology of ATP-sensitive K+ channels: interactions between glyburide and K+ channel openers.
    Meisheri KD, Khan SA, Martin JL.
    J Vasc Res; 1993 Oct; 30(1):2-12. PubMed ID: 8435468
    [Abstract] [Full Text] [Related]

  • 5. Functional receptors in Xenopus oocytes for U-37883A, a novel ATP-sensitive K+ channel blocker: comparison with rat insulinoma cells.
    Guillemare E, Honore E, De Weille J, Fosset M, Lazdunski M, Meisheri K.
    Mol Pharmacol; 1994 Jul; 46(1):139-45. PubMed ID: 8058048
    [Abstract] [Full Text] [Related]

  • 6. Cardiovascular effects of the K-ATP channel blocker U-37883A and structurally related morpholinoguanidines.
    Humphrey SJ, Smith MP, Cimini MG, Buchanan LV, Gibson JK, Khan SA, Meisheri KD.
    Methods Find Exp Clin Pharmacol; 1996 May; 18(4):247-60. PubMed ID: 8803957
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  • 8. Interaction of the diuretics torasemide and U-37883A with the K(ATP) channel in rat isolated aorta.
    Löffler-Walz C, Quast U.
    Naunyn Schmiedebergs Arch Pharmacol; 1998 Aug; 358(2):230-7. PubMed ID: 9750009
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  • 10. Effects of U-37883A, a vascular selective KATP+ channel antagonist, in the pulmonary and hindlimb circulation.
    DeWitt BJ, Cheng DY, McMahon TJ, Marrone JR, Champion HC, Kandowitz PJ.
    Am J Physiol; 1996 Dec; 271(6 Pt 1):L924-31. PubMed ID: 8997262
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  • 12. Effects of several potassium channel openers and glibenclamide on the uterus of the rat.
    Piper I, Minshall E, Downing SJ, Hollingsworth M, Sadraei H.
    Br J Pharmacol; 1990 Dec; 101(4):901-7. PubMed ID: 2128195
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  • 13. K(ATP) channel expression and pharmacological in vivo and in vitro studies of the K(ATP) channel blocker PNU-37883A in rat middle meningeal arteries.
    Ploug KB, Boni LJ, Baun M, Hay-Schmidt A, Olesen J, Jansen-Olesen I.
    Br J Pharmacol; 2008 May; 154(1):72-81. PubMed ID: 18332850
    [Abstract] [Full Text] [Related]

  • 14. Guanidine derivative U-37883A, inhibits mitochondrial K+ uniport.
    Szewczyk A, Wójcik G, Jabłonowska A, Nałecz.
    Pol J Pharmacol; 1995 May; 47(4):339-44. PubMed ID: 8616514
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  • 16. Multiple actions of U-37883A, an ATP-sensitive K+ channel blocker, on membrane currents in pig urethra.
    Tomoda T, Yunoki T, Naito S, Ito Y, Teramoto N.
    Eur J Pharmacol; 2005 Nov 07; 524(1-3):1-10. PubMed ID: 16242124
    [Abstract] [Full Text] [Related]

  • 17. Lack of effect of potassium channel openers on ATP-modulated potassium channels recorded from rat ventromedial hypothalamic neurones.
    Sellers AJ, Boden PR, Ashford ML.
    Br J Pharmacol; 1992 Dec 07; 107(4):1068-74. PubMed ID: 1467829
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  • 18. Epithelium-dependent inhibition of cholinergic transmission in rat isolated trachea by potassium channel openers.
    Fabiani ME, Vlahos R, Story DF.
    Pharmacol Res; 1996 Dec 07; 33(4-5):261-72. PubMed ID: 8938019
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