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Voltage-gated Potassium (KV) Channels
More Information »Voltage-gated potassium channels (KV) belong to the 6-TM family of potassium channel that also comprises the Ca2+-activated Slo (actually 7-TM) and the Ca2+-activated SK subfamilies. The α-subunits contain a single pore-forming region and combine to form tetramers.
Voltage-gated Potassium (KV) Channel Products
Activators |
|
Cat.No. |
Product Name / Activity |
| 2867 | Flupirtine maleate |
| KV7 channel activator | |
| 4305 | ICA 069673 |
| KV7.2/KV7.3 channel opener | |
| 2660 | L-364,373 |
| KV7.1 channel activator, activates IKs | |
| 4519 | ML 213 |
| KV7.2 and KV7.4 channel opener | |
| 3062 | NS 1643 |
| KV11.1 (hERG) channel activator. Antiarrhythmic | |
| 4462 | NS 3623 |
| KV11.1 (hERG) channel activator. Antiarrhythmic | |
| 4166 | NS 5806 |
| KV4.3 channel activator | |
| 2830 | PD 118057 |
| Selective KV11.1 (hERG) channel activator | |
Blockers |
|
Cat.No. |
Product Name / Activity |
| 4812 |
ADWX 1
|
| Potent and selective KV1.3 channel blocker | |
| 0876 | AM 92016 hydrochloride |
| KV channel blocker | |
| 0940 | 4-Aminopyridine |
| Non-selective KV channel blocker | |
| 3489 | Astemizole |
| Potent KV11.1 (hERG) channel blocker. Also histamine H1 antagonist | |
| 2787 | BAPTA AM |
| hKV11.1 (hERG), hKV1.3 and hKV1.5 channel blocker. Also Ca2+ chelator | |
| 1412 | Chromanol 293B |
| IKs blocker. Also blocks ICFTR | |
| 1475 | (-)-[3R,4S]-Chromanol 293B |
| IKs blocker. Enantiomer of Chromanol 293B (Cat. No. 1412) | |
| 1399 | CP 339818 hydrochloride |
| Non-peptide, potent KV1.3 channel blocker | |
| 3757 | Dofetilide |
| KV11.1 (hERG) channel blocker; inhibits rapid delayed rectifier K+ current (IKr) | |
| 2533 | DPO-1 |
| Blocker of KV1.5 channel and IKur current | |
| 1808 | E-4031 dihydrochloride |
| KV11.1 (hERG) channel blocker; inhibits rapid delayed rectifier K+ current (IKr) | |
| 3899 | JNJ 303 |
| Potent and selective IKs blocker | |
| 3564 | Kaliotoxin |
| KV and KCa blocker | |
| 1278 | KN-93 |
| K+ channel blocker (KV). Also inhibitor of CaM Kinase II | |
| 1999 | Linopirdine dihydrochloride |
| KV7 (KCNQ) channel blocker | |
| 3563 | Margatoxin |
| Potent KV1.3 channel blocker | |
| 4665 | ProTx I |
| CaV3.1 channel blocker; also inhibits NaV1.8 and KV2.1 | |
| 4367 | Psora 4 |
| Potent KV1.3 channel blocker | |
| 3557 | RuBi-4AP |
| Caged 4-aminopyridine; a non-selective KV channel blocker | |
| 3948 | Terfenadine |
| KV11.1 (hERG) and Kir6 (KATP) channel blocker. Also H1 antagonist | |
| 3829 | UK 78282 hydrochloride |
| Blocker of KV1.3 and KV1.4 channels | |
| 2000 | XE 991 dihydrochloride |
| Potent, selective KCNQ channel blocker; blocks M-current | |
Other |
|
Cat.No. |
Product Name / Activity |
| 2007 | Fluticasone propionate |
| Selective glucocorticoid agonist; KV1 potentiator | |
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