30 Results for "

KV11.1

" in MedChemExpress (MCE) Product Catalog:
Products (30)

30 Results for "KV11.1" in MCE Product Catalog:

1
1 Cited Publications
Cat. No.: HY-P1280
CAS No.: 145808-47-5
Margatoxin, an alpha-KTx scorpion toxin, is a high affinity inhibitor of Kv1.3 (Kd=11.7 pM). Margatoxin inhibits the Kv1.2 (Kd=6.4 pM) and Kv1.1 (Kd=4.2 nM). Margatoxin, a 39 amino-acid-long peptide, is isolated from the venom of the scorpion Centruroides margaritatus and widely used in ion channel research .
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Cat. No.: HY-108586
CAS No.: 343630-41-1
Purity:  ≥99.0%
Target:  

Potassium Channel

Research Areas:  

Neurological Disease

NS3623 is an activator of human ether-a-go-go-related gene (hERG1/KV11.1) potassium channels. NS3623 activates the IKr and Ito currents and has antiarrhythmic effect. NS3623 has a dual mode of action, being an inhibitor of hERG1 channels .
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Cat. No.: HY-108574
CAS No.: 478341-55-8
Purity:  99.61%
Research Areas:  

Neurological Disease

CP 339818 hydrochloride is a non-peptide Kv1.3 channel (IC50 = 200 nM) and Kv1.4 channel blocker. CP 339818 hydrochloride inhibits HCN channel with IC50s of 18.9 μM and 43.4 μM against HCN1 and HCN4 (high Cl -). CP 339818 hydrochloride has significantly weaker blocking effects on Kv1.1, Kv1.2, Kv1.5, Kv1.6, Kv3.1-4, and Kv4.2 channels. CP 339818 hydrochloride selectively blocked Kv1.3, thereby inhibiting the activation process of human T cells. CP 339818 hydrochloride can be used to study the physiological functions of HCN and Kv channels .
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Cat. No.: HY-137986
CAS No.: 1821638-43-0
Purity:  98.9%
Target:  

Potassium Channel

Research Areas:  

Inflammation/Immunology

LUF7244 is a selective allosteric modulator of Kv11.1 channels. LUF7244 inhibits early afterdepolarizations. LUF7244 can be used for anti-arrhythmia research .
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Cat. No.: HY-P3089A
Target:  

Potassium Channel

Research Areas:  

Others

Dendrotoxin K TFA is a Kv1.1 channel blocker. Dendrotoxin K TFA determines glutamate release in CA3 neurons in a time-dependent manner through the control of the presynaptic spike waveform .
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Cat. No.: HY-P3055A
Synonyms: DTX-I TFA
Target:  

Potassium Channel

Research Areas:  

Cancer

Dendrotoxin-I (DTX-I) TFA is a potent K + channel blocker with IC50s of 0.13-50 nM for voltage-gated potassium channel subunits KV1.1, KV1.2 and KV1.6. Dendrotoxin-I TFA, a neurotoxin, has the potential for cancer research .
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Cat. No.: HY-120375
CAS No.: 1821638-40-7
Target:  

Potassium Channel

Research Areas:  

Cardiovascular Disease

LUF7346 is a potent Kv11.1 (hERG) channel negative allosteric modulator, with an IC50 of 35.6 ± 3.2 nM .
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Cat. No.: HY-P2707
CAS No.: 74504-53-3
Synonyms: α-DTX
Research Areas:  

Neurological Disease

α-Dendrotoxin (α-DTX) is a voltage-gated K + channel blocker and an acid-sensing ion channel (ASIC) inhibitor. α-Dendrotoxin blocks Kv1.1, Kv1.2, Kv1.6 and D-type (ID) voltage-gated K + channels, and reversibly inhibits slowly inactivating potassium currents. α-Dendrotoxin induces epilepsy-related behaviors in mice. α-Dendrotoxin can be used in studies related to tonic-clonic seizures .
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Cat. No.: HY-P1440A
Target:  

Potassium Channel

Research Areas:  

Neurological Disease

BeKm-1 TFA is a potent and selective KV11.1 (hERG) channel blocker. BeKm-1 TFA is selective for KV11.1 over a panel of 14 other potassium channels. BeKm-1 TFA dose-dependently prolongs QTc interval in isolated rabbit heart.
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Cat. No.: HY-P3055
CAS No.: 107950-33-4
Synonyms: DTX-I
Dendrotoxin-I (DTX-I) is a potent K + channels blocker with IC50s of 0.13-50 nM for voltage-gated potassium channel subunits KV1.1, KV1.2 and KV1.6, respectively. Dendrotoxin-I, a neurotoxin, has the potential for cancer research .
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Cat. No.: HY-116759
CAS No.: 712325-30-9
Purity:  99.93%
Target:  

Potassium Channel

Research Areas:  

Cardiovascular Disease

VU0405601 is a potent KV11.1 channel activator. VU0405601 protects cardiac tissue from dofetilide (HY-B0232)-induced ventricular tachycardia .
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Cat. No.: HY-126106
CAS No.: 622011-16-9
Target:  

Potassium Channel

Research Areas:  

Others

(BrMT)2 (compound 2) is a non-peptide snail toxin that slows down the activation of Kv1.1 channels .
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Cat. No.: HY-RS07184
Research Areas:  

Others

KCNV2 Human Pre-designed siRNA Set A contains three designed siRNAs for KCNV2 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-P3089
CAS No.: 119128-61-9
Target:  

Potassium Channel

Research Areas:  

Others

Dendrotoxin K is a Kv1.1 channel blocker. Dendrotoxin K determines glutamate release in CA3 neurons in a time-dependent manner through the control of the presynaptic spike waveform .
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Cat. No.: HY-P5788
Target:  

Potassium Channel

Research Areas:  

Neurological Disease

Hemitoxin, a scorpion-venom peptide, is a K + channel blocker. Hemitoxin blocks rat Kv1.1, Kv1.2 and Kv1.3 channels expressed in Xenopus oocytes with IC50 values of 13 nM, 16 nM and 2 nM, respectively .
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Cat. No.: HY-113673
CAS No.: 1031335-85-9
Purity:  98.77%
Target:  

Potassium Channel

Research Areas:  

Cardiovascular Disease

A-935142 is a human ether-a-go-go-related gene (hERG, Kv 11.1) channel activator. A-935142 enhances hERG current in a complex manner by facilitation of activation, reduction of inactivation, and slowing of deactivation, and abbreviates atrial and ventricular repolarization .
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Cat. No.: HY-P5853
Target:  

Potassium Channel

Research Areas:  

Inflammation/Immunology

Aam-KTX is a Kv channel inhibitor with IC50 values of 1.1 nM and >750 nM for Kv1.3 and Kv1.1, respectively. Aam-KTX is a toxic peptide obtained from the venom of the scorpion Mesobuthus eupeus. Aam-KTX has potential in autoimmune diseases research .
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Cat. No.: HY-P3014
Target:  

Potassium Channel

Research Areas:  

Others

Hongotoxin-1, isolated from venom of Centruroides limbatus, is the inhibitor of potassium channel, with IC50 for? Kv1.1, Kv1.2, Kv1.3, and Kv1.6 of 31 pM, 170 pM, 86 pM,and 6000 pM, respectively .
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Cat. No.: HY-RS07126
Research Areas:  

Others

KCNH2 Human Pre-designed siRNA Set A contains three designed siRNAs for KCNH2 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-P5771
Target:  

Sodium Channel

Research Areas:  

Neurological Disease

Jingzhaotoxin-IX, a C-terminally amidated peptide composed of 35 amino acid residues, is a neurotoxin. Jingzhaotoxin-IX inhibits voltage-gated sodium channels (both tetrodotoxin-resistant and tetrodotoxin-sensitive isoforms) and Kv2.1 channel. Jingzhaotoxin-IX has no effect on delayed rectifier potassium channel Kv1.1, 1.2 and 1.3 .
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