Dihydropyrazolopyrimidine Inhibitors of KV1.5 (IKur)
摘要:
A series of dihydropyrazolopyrimidine inhibitors of K(V)1.5 (I-Kur) have been identified. The synthesis, structure-activity relationships and selectivity against several other ion channels are described. (C) 2008 Elsevier Ltd. All rights reserved.
Novel heterocyclic dihydropyrimidine compounds useful as inhibitors of potassium channel function (especially inhibitors of the K
v
1 subfamily of voltage gated K
+
channels, especially inhibitors K
v
1.5 which has been linked to the ultra-rapidly activating delayed rectifier K
+
current I
Kur
), methods of using such compounds in the prevention and treatment of arrhythmia and I
Kur
-associated conditions, and pharmaceutical compositions containing such compounds.
US7157451B2
申请人:——
公开号:US7157451B2
公开(公告)日:2007-01-02
US7541362B2
申请人:——
公开号:US7541362B2
公开(公告)日:2009-06-02
Dihydropyrazolopyrimidine Inhibitors of KV1.5 (IKur)
作者:Wayne Vaccaro、Tram Huynh、John Lloyd、Karnail Atwal、Heather J. Finlay、Paul Levesque、Mary Lee Conder、Tonya Jenkins-West、Hong Shi、Lucy Sun
DOI:10.1016/j.bmcl.2008.10.099
日期:2008.12
A series of dihydropyrazolopyrimidine inhibitors of K(V)1.5 (I-Kur) have been identified. The synthesis, structure-activity relationships and selectivity against several other ion channels are described. (C) 2008 Elsevier Ltd. All rights reserved.