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Journal Abstract Search

153 related items for PubMed ID: 35521179

  • 21.
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  • 22. Comparison of potent Kv1.5 potassium channel inhibitors reveals the molecular basis for blocking kinetics and binding mode.
    Strutz-Seebohm N, Gutcher I, Decher N, Steinmeyer K, Lang F, Seebohm G.
    Cell Physiol Biochem; 2007; 20(6):791-800. PubMed ID: 17982261
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  • 23. The 'functional' dyad of scorpion toxin Pi1 is not itself a prerequisite for toxin binding to the voltage-gated Kv1.2 potassium channels.
    Mouhat S, Mosbah A, Visan V, Wulff H, Delepierre M, Darbon H, Grissmer S, De Waard M, Sabatier JM.
    Biochem J; 2004 Jan 01; 377(Pt 1):25-36. PubMed ID: 12962541
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  • 24. A blue-green alga from Okinawa contains aplysiatoxins, the third class of tumor promoters.
    Fujiki H, Ikegami K, Hakii H, Suganuma M, Yamaizumi Z, Yamazato K, Moore RE, Sugimura T.
    Jpn J Cancer Res; 1985 Apr 01; 76(4):257-9. PubMed ID: 3924698
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  • 27. Molecular dynamics of Kv1.3 ion channel and structural basis of its inhibition by scorpion toxin-OSK1 derivatives.
    Bhuyan R, Seal A.
    Biophys Chem; 2015 Apr 01; 203-204():1-11. PubMed ID: 26001067
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  • 31. Identification, synthesis, and activity of novel blockers of the voltage-gated potassium channel Kv1.5.
    Peukert S, Brendel J, Pirard B, Brüggemann A, Below P, Kleemann HW, Hemmerle H, Schmidt W.
    J Med Chem; 2003 Feb 13; 46(4):486-98. PubMed ID: 12570371
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  • 34. Structural basis of the potency and selectivity of Urotoxin, a potent Kv1 blocker from scorpion venom.
    Luna-Ramirez K, Csoti A, McArthur JR, Chin YKY, Anangi R, Najera RDC, Possani LD, King GF, Panyi G, Yu H, Adams DJ, Finol-Urdaneta RK.
    Biochem Pharmacol; 2020 Apr 13; 174():113782. PubMed ID: 31881193
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  • 35. Loss of the Phenolic Hydroxyl Group and Aromaticity from the Side Chain of Anti-Proliferative 10-Methyl-aplog-1, a Simplified Analog of Aplysiatoxin, Enhances Its Tumor-Promoting and Proinflammatory Activities.
    Hanaki Y, Kikumori M, Tokuda H, Okamura M, Dan S, Adachi N, Saito N, Yanagita RC, Irie K.
    Molecules; 2017 Apr 13; 22(4):. PubMed ID: 28406454
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  • 36. Hg1, novel peptide inhibitor specific for Kv1.3 channels from first scorpion Kunitz-type potassium channel toxin family.
    Chen ZY, Hu YT, Yang WS, He YW, Feng J, Wang B, Zhao RM, Ding JP, Cao ZJ, Li WX, Wu YL.
    J Biol Chem; 2012 Apr 20; 287(17):13813-21. PubMed ID: 22354971
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  • 39. In silico detection of binding mode of J-superfamily conotoxin pl14a with Kv1.6 channel.
    Mondal S, Babu RM, Bhavna R, Ramakumar S.
    In Silico Biol; 2007 Apr 20; 7(2):175-86. PubMed ID: 17688443
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  • 40. Molecular mechanism of the sea anemone toxin ShK recognizing the Kv1.3 channel explored by docking and molecular dynamic simulations.
    Jin L, Wu Y.
    J Chem Inf Model; 2007 Apr 20; 47(5):1967-72. PubMed ID: 17718553
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