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本文引用的文献

1
Irreversible block of cardiac mutant Na+ channels by batrachotoxin.蟾毒素对心脏突变型钠离子通道的不可逆阻断。
Channels (Austin). 2007 May-Jun;1(3):179-88. doi: 10.4161/chan.4437. Epub 2007 May 15.
2
N-(6-chloro-pyridin-3-yl)-3,4-difluoro-benzamide (ICA-27243): a novel, selective KCNQ2/Q3 potassium channel activator.N-（6-氯吡啶-3-基）-3,4-二氟苯甲酰胺（ICA-27243）：一种新型的选择性KCNQ2/Q3钾通道激活剂。
Mol Pharmacol. 2008 Mar;73(3):977-86. doi: 10.1124/mol.107.043216. Epub 2007 Dec 18.
3
The D-diastereomer of ShK toxin selectively blocks voltage-gated K+ channels and inhibits T lymphocyte proliferation.ShK毒素的D-非对映异构体选择性阻断电压门控性钾通道并抑制T淋巴细胞增殖。
J Biol Chem. 2008 Jan 11;283(2):988-97. doi: 10.1074/jbc.M706008200. Epub 2007 Nov 5.
4
Pharmacokinetics, toxicity, and functional studies of the selective Kv1.3 channel blocker 5-(4-phenoxybutoxy)psoralen in rhesus macaques.恒河猴中选择性Kv1.3通道阻滞剂5-(4-苯氧基丁氧基)补骨脂素的药代动力学、毒性及功能研究
Exp Biol Med (Maywood). 2007 Nov;232(10):1338-54. doi: 10.3181/0705-RM-148.
5
Calcium signalling in lymphocyte activation and disease.淋巴细胞激活与疾病中的钙信号传导
Nat Rev Immunol. 2007 Sep;7(9):690-702. doi: 10.1038/nri2152. Epub 2007 Aug 17.
6
Targeting effector memory T-cells with Kv1.3 blockers.用Kv1.3阻滞剂靶向效应记忆T细胞。
Curr Opin Drug Discov Devel. 2007 Jul;10(4):438-45.
7
Therapeutic potential of neuronal two-pore domain potassium-channel modulators.神经元双孔结构域钾通道调节剂的治疗潜力
Curr Opin Investig Drugs. 2007 Jul;8(7):555-62.
8
The small molecule NS11021 is a potent and specific activator of Ca2+-activated big-conductance K+ channels.小分子NS11021是一种有效的、特异性的Ca2+激活的大电导K+通道激活剂。
Mol Pharmacol. 2007 Oct;72(4):1033-44. doi: 10.1124/mol.107.038331. Epub 2007 Jul 16.
9
Electrophysiology of the phagocyte respiratory burst. Focus on "Large-conductance calcium-activated potassium channel activity is absent in human and mouse neutrophils and is not required for innate immunity".吞噬细胞呼吸爆发的电生理学。聚焦于“人类和小鼠中性粒细胞中不存在大电导钙激活钾通道活性，且先天免疫不需要该通道活性”
Am J Physiol Cell Physiol. 2007 Jul;293(1):C30-2. doi: 10.1152/ajpcell.00093.2007.
10
Modulators of small- and intermediate-conductance calcium-activated potassium channels and their therapeutic indications.小电导和中电导钙激活钾通道调节剂及其治疗适应症。
Curr Med Chem. 2007;14(13):1437-57. doi: 10.2174/092986707780831186.

K+ channel modulators for the treatment of neurological disorders and autoimmune diseases.

作者信息

Wulff Heike, Zhorov Boris S

机构信息

Department of Pharmacology, University of California, Davis, California 95616, USA.

出版信息

Chem Rev. 2008 May;108(5):1744-73. doi: 10.1021/cr078234p.

DOI:10.1021/cr078234p
PMID:18476673
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2714671/
Abstract
摘要