7 Results for "

KV2.2

" in MedChemExpress (MCE) Product Catalog:
Products (7)

7 Results for "KV2.2" in MCE Product Catalog:

2
2 Cited Publications
Cat. No.: HY-120033
CAS No.: 1393441-53-6
Purity:  98.59%
Target:  

Sodium Channel

Research Areas:  

Neurological Disease

RY796 is a potent and selective voltage-gated potassium (KV2) channel inhibitor with IC50s of 0.25 μM and 0.09 μM for KV2.1 and KV2.2. RY796 has analgesic activity .
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Cat. No.: HY-114608
CAS No.: 1393748-80-5
Purity:  97.00%
Target:  

Sodium Channel

Research Areas:  

Neurological Disease

RY785 is a potent and selective voltage-gated potassium (KV2) channel inhibitor with an IC50 of 0.05 μM for KV2.2. RY785 has analgesic activity .
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Cat. No.: HY-P1427A
Target:  

Potassium Channel

Research Areas:  

Neurological Disease

Guangxitoxin 1E TFA is the TFA salt form of Guangxitoxin 1E (HY-P1427). Guangxitoxin 1E TFA is a peptide toxin and a selective inhibitor for voltage-gated potassium channel KV2.1 and KV2.2 with IC50 of 1-3 nM. Guangxitoxin 1E TFA enhances glucose-stimulated intracellular calcium ion oscillations and increases insulin secretion in a glucose-dependent manner .
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Cat. No.: HY-44153
CAS No.: 689297-68-5
Target:  

Potassium Channel

Research Areas:  

Neurological Disease

KV2 channel inhibitor-1 is a selective KV2 channel inhibitor with IC50s of 0.2 μM and 0.41 μM for KV2.1 and KV2.2, respectively. KV2 channel inhibitor-1 possesses good selectivity over KV1.2 (IC50>10 μM). KV2 channel inhibitor-1 is >10-fold selective over NaV channels and other KV channels and displays weak activity on CaV channels .
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Cat. No.: HY-P1427
CAS No.: 1233152-82-3
Target:  

Potassium Channel

Research Areas:  

Neurological Disease

Guangxitoxin 1E is a potent and selective blocker of KV2.1 and KV2.2 channels. Guangxitoxin 1E inhibits KV2 with an IC50 of 1-3 nM. KV2 channels underlie delayed-rectifier potassium currents in various neurons .
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Cat. No.: HY-P5155
CAS No.: 741738-59-0
Target:  

Potassium Channel

Research Areas:  

Neurological Disease

Stromatoxin 1 is an inhibitor of Potassium Channel, a peptide which can be isolated from tarantulas. Stromatoxin 1 selectively inhibits K(V)2.1, K(V)2.2, K(V)4.2, and K(V)2.1/9.3 channels. K(V)2.1 and K(V)2.2, but not K(V)4.2, channel subunits play a key role in opposing both myogenic and neurogenic urinary bladder smooth muscle (UBSM) contractions in rats .
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Cat. No.: HY-RS07107
Research Areas:  

Others

KCNB2 Human Pre-designed siRNA Set A contains three designed siRNAs for KCNB2 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

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