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)
- GC17661E-4031 dihydrochlorideCAS: 113559-13-0纯度: >98.50%
An antiarrhythmic, ERG potassium channel blocker
- GC17739PNU 37883 hydrochlorideCAS: 57568-80-6
PNU 37883 hydrochloride (PNU 37883A) 是一种选择性血管 ATP 敏感性钾 (Kir6, KATP) 通道阻滞剂。
- GC17787UK 78282 hydrochlorideCAS: 136647-02-4
KV1.3 and KV1.4 voltage-gated potassium channel blocker
- GC30267Pinacidil monohydrateCAS: 85371-64-8纯度: >99.00% / >98.00%
Pinacidil monohydrate一种抗高血压药物,属于钾通道开放剂,通过激活ATP敏感性钾通道使血管平滑肌松弛。
- GC30280Chlorpromazine D6 hydrochlorideCAS: 1228182-46-4纯度: >99.50%
Chlorpromazine D6 hydrochloride是 Chlorpromazine 的氘代物,可被用于 NMR、GC-MS 或 LC-MS 分析中的内标品,用于定量分析。
- GC30891Almitrine mesylate (Almitrine bismesylate)CAS: 29608-49-9纯度: >98.00%
Almitrine mesylate (Almitrine bismesylate, Almitrine dimethanesulfonate, Almitrine dimesylate), a pharmacologically unique respiratory stimulant, acts as an agonist of peripheral chemoreceptors located on the carotid bodies. Almitrine mesylate inhibits the activity of Ca2+-dependent K+ channel by decreasing its open probability with IC50 of 0.22 μM.
| 货号 | 产品名称 | CAS号 | 纯度 | 结构 |
|---|---|---|---|---|
| GC16690 | Y-27152 | 127408-30-4 | - | |
Y-27152 是 KATP (Kir6) 通道开放剂 Y-26763 的前药,是一种长效的 K+ 通道开放剂,具有较少的心动过速:对清醒状态的高血压大鼠和狗的抗高血压作用。 | ||||
| GC16717 | 1-EBIO | 10045-45-1 | >99.50% | |
An activator of KCa channels | ||||
| GC16848 | P1075 | 60559-98-0 | >97.00% | |
P1075是一种有效的、磺酰脲受体2相关的ATP敏感性的钾通道(SUR2-K IR 6) 的激活剂,EC 50 值为45±10nM。 | ||||
| GC16945 | Astemizole | 68844-77-9 | >99.50% | |
Astemizole是一种强效抗组胺化合物,可拮抗组胺H1受体,IC 50 值为4nM。 | ||||
| GC16948 | Valinomycin | 2001-95-8 | >98.00% / >95.00% | |
缬霉素Valinomycin是一种十二肽抗生素,从几种链霉菌菌株中获得。 | ||||
| GC17001 | Verruculogen | 12771-72-1 | >95.00% | |
A tremorgenic mycotoxin | ||||
| GC17264 | ZM 226600 | 147695-92-9 | - | |
Kir6 (KATP) channel opener | ||||
| GC17272 | Charybdotoxin | 95751-30-7 | - | |
A blocker of K+ channels | ||||
| GC17280 | NS 5806 | 426834-69-7 | >98.00% | |
An I to current activator | ||||
| GC17518 | YS-035 hydrochloride | 89805-39-0 | - | |
A calcium channel blocker | ||||
| GC17595 | CP 339818 hydrochloride | 478341-55-8 | - | |
KV1.3 channel antagonist | ||||
| GC17661 | E-4031 dihydrochloride | 113559-13-0 | >98.50% | |
An antiarrhythmic, ERG potassium channel blocker | ||||
| GC17739 | PNU 37883 hydrochloride | 57568-80-6 | - | |
PNU 37883 hydrochloride (PNU 37883A) 是一种选择性血管 ATP 敏感性钾 (Kir6, KATP) 通道阻滞剂。 | ||||
| GC17787 | UK 78282 hydrochloride | 136647-02-4 | - | |
KV1.3 and KV1.4 voltage-gated potassium channel blocker | ||||
| GC17909 | NS 6180 | 353262-04-1 | >99.50% | |
An inhibitor of IKCa1/K Ca 3.1 channels | ||||
| GC18203 | Annonacin | 111035-65-5 | >98.00% | |
A mitochondrial complex I inhibitor | ||||
| GC18210 | GAL-021 | 1380341-99-0 | >98.00% | |
A BK Ca channel blocker | ||||
| GC18629 | VU0071063 | 333415-38-6 | >99.00% | |
A K ir 6.2/SUR1 activator | ||||
| GC19004 | SKA-121 | 1820708-73-3 | >99.00% | |
A positive-gating modulator of IKCa1/K Ca 3.1 channels | ||||
| GC19183 | GSK369796 Dihydrochloride | 1010411-21-8 | >98.00% | |
An antimalarial agent | ||||
| GC19480 | AUT1 | 1311136-84-1 | >99.50% | |
A positive modulator of K v 3.1b, K v 3.2a, and K v 3.3 | ||||
| GC30267 | Pinacidil monohydrate | 85371-64-8 | >99.00% / >98.00% | |
Pinacidil monohydrate一种抗高血压药物,属于钾通道开放剂,通过激活ATP敏感性钾通道使血管平滑肌松弛。 | ||||
| GC30280 | Chlorpromazine D6 hydrochloride | 1228182-46-4 | >99.50% | |
Chlorpromazine D6 hydrochloride是 Chlorpromazine 的氘代物,可被用于 NMR、GC-MS 或 LC-MS 分析中的内标品,用于定量分析。 | ||||
| GC30891 | Almitrine mesylate (Almitrine bismesylate) | 29608-49-9 | >98.00% | |
Almitrine mesylate (Almitrine bismesylate, Almitrine dimethanesulfonate, Almitrine dimesylate), a pharmacologically unique respiratory stimulant, acts as an agonist of peripheral chemoreceptors located on the carotid bodies. Almitrine mesylate inhibits the activity of Ca2+-dependent K+ channel by decreasing its open probability with IC50 of 0.22 μM. | ||||
