Literature DB >> 17350840

Aryl sulfonamido indane inhibitors of the Kv1.5 ion channel.

Michael F Gross1, Serge Beaudoin, Grant McNaughton-Smith, George S Amato, Neil A Castle, Christine Huang, Anruo Zou, Weifeng Yu.   

Abstract

A collection of aryl sulfonamido indanes based on the lead compound 1 was synthesized and evaluated for Kv1.5 inhibitory activity. Kv1.5 inhibitors have the potential to be atrium-selective agents for treatment of atrial fibrillation. (1R,2R)-1 has an IC(50) of 0.033microM against Kv1.5 and is selective against other cardiac ion channels, including hERG.

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Year:  2007        PMID: 17350840     DOI: 10.1016/j.bmcl.2007.02.052

Source DB:  PubMed          Journal:  Bioorg Med Chem Lett        ISSN: 0960-894X            Impact factor:   2.823


  2 in total

1.  Identification, Synthesis, and Biological Evaluation of the Major Human Metabolite of NLRP3 Inflammasome Inhibitor MCC950.

Authors:  Manohar Salla; Mark S Butler; Ruby Pelingon; Geraldine Kaeslin; Daniel E Croker; Janet C Reid; Jong Min Baek; Paul V Bernhardt; Elizabeth M J Gillam; Matthew A Cooper; Avril A B Robertson
Journal:  ACS Med Chem Lett       Date:  2016-09-27       Impact factor: 4.345

Review 2.  Voltage-gated potassium channels as therapeutic targets.

Authors:  Heike Wulff; Neil A Castle; Luis A Pardo
Journal:  Nat Rev Drug Discov       Date:  2009-12       Impact factor: 84.694

  2 in total

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