Potassium Channel
Potassium Channel(钾离子通道)
Potassium channels are voltage-gated ion channels that selectively permeate potassium ion through the excitable membrane. It regulates the release of neurotransmitters, insulin secretion, smooth muscle contraction and heart rate etc.
Potassium Channel 相关产品(302)
- GC13455VU 591 hydrochlorideCAS: 1315380-70-1纯度: >98.00%
VU 591 hydrochloride 是一种有效的、选择性的肾外髓质钾通道 (ROMK 或 Kir1.1) 抑制剂,IC50 为 0.24 μM。
- GC14044(-)-[3R,4S]-Chromanol 293BCAS: 163163-24-4
(-)-[3R,4S]-Chromanol 293B 是延迟整流器 K+ 电流 (IKs) 的慢速成分的有效选择性抑制剂。
- GC14216Chlorpromazine HClCAS: 69-09-0纯度: >99.50%
Chlorpromazine HCl是一种口服有效的、可透过血脑屏障的吩噻嗪类抗精神病药,能够有效抑制D2多巴胺受体和5-HT 2A ,具有很强的镇静作用。
- GC14703Oxybutynin chlorideCAS: 1508-65-2纯度: >98.00%
An antagonist of muscarinic acetylcholine receptors
| 货号 | 产品名称 | CAS号 | 纯度 | 结构 |
|---|---|---|---|---|
| GC12547 | NS 1619 | 153587-01-0 | >98.00% | |
NS 1619是一种选择性的大电导钙激活钾通道激活剂。 | ||||
| GC12575 | DPO-1 | 43077-30-1 | - | |
An inhibitor of K v 1.5 channels | ||||
| GC13188 | UCL 2077 | 918311-87-2 | - | |
UCL 2077 是一种选择性慢后超极化 (sAHP) 通道阻滞剂(在培养的海马神经元中 IC50 =500 nM),对超极化后的 Ca2+ 通道、动作电位、输入电阻和介质影响最小。 | ||||
| GC13323 | BDS I | - | - | |
Kv3.4 potassium channel blocker, potent and reversible | ||||
| GC13353 | Spadin | 1270083-24-3 | >99.00% | |
An inhibitor of K 2P 2.1/TREK1 | ||||
| GC13455 | VU 591 hydrochloride | 1315380-70-1 | >98.00% | |
VU 591 hydrochloride 是一种有效的、选择性的肾外髓质钾通道 (ROMK 或 Kir1.1) 抑制剂,IC50 为 0.24 μM。 | ||||
| GC13466 | Flufenamic acid | 530-78-9 | >99.50% | |
An NSAID and COX inhibitor | ||||
| GC13490 | E-4031 | 113558-89-7 | >99.00% | |
An antiarrhythmic, ERG potassium channel blocker | ||||
| GC13819 | Tertiapin LQ | - | - | |
Kir1.1 channel blocker | ||||
| GC13976 | Doxapram hydrochloride hydrate | 7081-53-0 | >99.50% | |
A central respiratory stimulant | ||||
| GC14029 | Retigabine | 150812-12-7 | - | |
Retigabine是一种抗惊厥化合物,可激活低阈值电压门控钾通道。 | ||||
| GC14044 | (-)-[3R,4S]-Chromanol 293B | 163163-24-4 | - | |
(-)-[3R,4S]-Chromanol 293B 是延迟整流器 K+ 电流 (IKs) 的慢速成分的有效选择性抑制剂。 | ||||
| GC14073 | DCPIB | 82749-70-0 | >99.50% | |
A VRAC inhibitor | ||||
| GC14113 | Oxybutynin | 5633-20-5 | >99.50% | |
An antagonist of muscarinic acetylcholine receptors | ||||
| GC14116 | Cromakalim | 94470-67-4 | - | |
A prototypical KATP channel activator | ||||
| GC14216 | Chlorpromazine HCl | 69-09-0 | >99.50% | |
Chlorpromazine HCl是一种口服有效的、可透过血脑屏障的吩噻嗪类抗精神病药,能够有效抑制D2多巴胺受体和5-HT 2A ,具有很强的镇静作用。 | ||||
| GC14239 | BMS 191011 | 202821-81-6 | >98.50% | |
A K Ca 1.1/BK channel activator | ||||
| GC14297 | ShK-Dap22 | 220384-25-8 | - | |
Extremely potent KV1.3 channel blocker | ||||
| GC14515 | Azimilide | 149908-53-2 | - | |
A class III antiarrhythmic agent | ||||
| GC14563 | Ketanserin | 74050-98-9 | >99.00% / >97.00% | |
A potent 5-HT 2 receptor antagonist | ||||
| GC14646 | RuBi-4AP | 851956-02-0 | - | |
voltage-dependent K+ channel blocker | ||||
| GC14703 | Oxybutynin chloride | 1508-65-2 | >98.00% | |
An antagonist of muscarinic acetylcholine receptors | ||||
| GC14705 | Tolbutamide Sodium | 473-41-6 | >98.00% | |
A SUR1/K ir 6.2 channel inhibitor | ||||
| GC14754 | Linopirdine dihydrochloride | 113168-57-3 | - | |
A neurotransmitter release enhancer | ||||
