位置：成果数据库 > 期刊 > 期刊详情页
The hERG Activator, NS1643, Enhances Epilepsy-Associated KCNQ Channels.
  • 期刊名称：JPET
  • 时间：2014.12
  • 页码：596-604
  • 相关项目：与神经系统疾病相关的离子通道的结构与功能研究
作者： Ping Li, Xueqin Chen, Qiansen Zhang, Yueming Zheng|
同期刊论文项目
与神经系统疾病相关的离子通道的结构与功能研究
期刊论文 29
同项目期刊论文
Design of Cell-Permeable Stapled-Peptides as HIV-1 Intergrase Inhibitors
Modulation of A(2)a receptor antagonist on D(2) receptor internalizationand ERK phosphorylation
Investigation on the 1,6-naphthyridine motif:discovery and SAR study of 1H-imidazo[4,5-h][1,6]naphth
P-Retigabine: a N-propargyled retigabine with improved brain distributionand enhanced antiepileptic
Novel KCNQ2 channel activators discovered using fluorescence-based andautomated patch-clamp-based hi
Protein kinase A rescues microtubule affinity-regulating kinase2-induced microtubule instability and
P-Retigabine: a N-propargyled retigabine with improved brain distribution and enhanced antiepileptic
Metabolically stabilized structural modification on the helix B surface peptide of erythropoietin:De
Ion channels gated by acetylcholine and serotonin: structures, biology, and drug discovery
3-Carboxyl-4-quinolones as cell-permeableinhibitors of protein tyrosine phosphatase 1B
Metal-Free TEMPO-Promoted C(sp3)–HAmination to Afford MultisubstitutedBenzimidazoles
Solvent/oxidant-switchable synthesis of multisubstitutedquinazolines andbenzimidazoles via metal-fre
Activation of peripheral KCNQ channels relieves gout pain
离子通道与肿瘤相关性的研究进展
DirectSynthesis of 2-Aryl-4-quinolones via Transition Metal-free IntramolecularOxidative C(sp3)-H/C(
Design and discovery of flavonoid-based HIV-1integrase inhibitors targeting both the active site and
Paeoniflorin ameliorates ischemic neuronal damage in vitro via adenosineA1 receptor-mediated transac
Connexin 43 stabilizes astrocytes in a stroke-like milieu to facilitateneuronal recovery
Repositioning HIV-1 integrase inhibitors for cancer therapeutics:1,6-naphthyridine-7-carboxamide as
LLDT-67 attenuates MPTP-induced neurotoxicity in mice by up-regulating NGF expression
 EZH2: biology, disease, and structure-based drug discovery
Discovery of a novel5-carbonyl-1H-imidazole-4-carboxamide class of inhibitors of the HIV-1integrase-
Crystallization scale purification of α7 nicotinic acetylcholine receptor from mammalian cells using