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Journal Abstract Search

71 related items for PubMed ID: 15588618

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  • 3. Pharmacological Profile of U-37883A, a Channel Blocker of Smooth Muscle-Type ATP-Sensitive K Channels.
    Teramoto N.
    Cardiovasc Drug Rev; 2006; 24(1):25-32. PubMed ID: 16939631
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  • 4. Multiple effects of mefenamic acid on K(+) currents in smooth muscle cells from pig proximal urethra.
    Teramoto N, Brading AF, Ito Y.
    Br J Pharmacol; 2003 Dec; 140(8):1341-50. PubMed ID: 14623761
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  • 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
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  • 6. 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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  • 7. [Properties of large-conductance calcium-activated potassium channel in rat mesenteric arteriole smooth muscle cells].
    Zhao GL, Pan BX, Huang XL, Zhao KS.
    Di Yi Jun Yi Da Xue Xue Bao; 2003 Aug; 23(8):786-90. PubMed ID: 12919898
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  • 8. The effects of flecainide on ATP-sensitive K(+) channels in pig urethral myocytes.
    Yunoki T, Teramoto N, Naito S, Ito Y.
    Br J Pharmacol; 2001 Jul; 133(5):730-8. PubMed ID: 11429398
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  • 9. Acetic acid opens large-conductance Ca2+-activated K+ channels in guinea pig detrusor smooth muscle cells.
    Ghatta S, Lozinskaya I, Lin Z, Gordon E, Willette RN, Brooks DP, Xu X.
    Eur J Pharmacol; 2007 Jun 01; 563(1-3):203-8. PubMed ID: 17382925
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  • 10. Receptor binding characterization in kidney membrane of [3H]U-37883, a novel ATP-sensitive K+ channel blocker with diuretic/natriuretic properties.
    Meisheri K, Fosset M, Humphrey S, Lazdunski M.
    Mol Pharmacol; 1995 Jan 01; 47(1):155-63. PubMed ID: 7838124
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  • 12. Guanidine derivative U-37883A, inhibits mitochondrial K+ uniport.
    Szewczyk A, Wójcik G, Jabłonowska A, Nałecz.
    Pol J Pharmacol; 1995 Jan 01; 47(4):339-44. PubMed ID: 8616514
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  • 13. 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 01; 266(2):655-65. PubMed ID: 8355199
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  • 16. The Na(+)/Ca(2+) exchanger inhibitor KB-R7943 activates large-conductance Ca(2+)-activated K(+) channels in endothelial and vascular smooth muscle cells.
    Liang GH, Kim JA, Seol GH, Choi S, Suh SH.
    Eur J Pharmacol; 2008 Mar 17; 582(1-3):35-41. PubMed ID: 18237728
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  • 17. The amiodarone derivative 2-methyl-3-(3,5-diiodo-4-carboxymethoxybenzyl)benzofuran (KB130015) opens large-conductance Ca2+-activated K+ channels and relaxes vascular smooth muscle.
    Gessner G, Heller R, Hoshi T, Heinemann SH.
    Eur J Pharmacol; 2007 Jan 26; 555(2-3):185-93. PubMed ID: 17134694
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  • 18. Aldosterone-induced coronary dysfunction in transgenic mice involves the calcium-activated potassium (BKCa) channels of vascular smooth muscle cells.
    Ambroisine ML, Favre J, Oliviero P, Rodriguez C, Gao J, Thuillez C, Samuel JL, Richard V, Delcayre C.
    Circulation; 2007 Nov 20; 116(21):2435-43. PubMed ID: 17984374
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  • 19. Angiotensin II activates intermediate-conductance Ca2+ -activated K+ channels in arterial smooth muscle cells.
    Hayabuchi Y, Nakaya Y, Yasui S, Mawatari K, Mori K, Suzuki M, Kagami S.
    J Mol Cell Cardiol; 2006 Dec 20; 41(6):972-9. PubMed ID: 16919291
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  • 20. Diuretic activity of N'-disubstituted morpholinoguanidine analogs of U-37883A in rats and dogs.
    Humphrey SJ, Ludens JH, Perricone SC, Skaletzky LL, Graham BE, Zins GR.
    Methods Find Exp Clin Pharmacol; 1995 May 20; 17(4):255-66. PubMed ID: 7475512
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