25 Results for "

IKs

" in MedChemExpress (MCE) Product Catalog:
Products (25)

25 Results for "IKs" in MCE Product Catalog:

2
2 Cited Publications
Cat. No.: HY-106369
CAS No.: 223749-46-0
Purity:  99.95%
Target:  

Potassium Channel

Research Areas:  

Cardiovascular Disease

HMR 1556, a chromanol derivative, is a potent IKs blocker with IC50s of 10.5 nM and 34 nM in canine and guinea pig left ventricular myocytes, respectively .
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2
2 Cited Publications
Cat. No.: HY-18600A
CAS No.: 149888-94-8
Synonyms: NE-10064 dihydrochloride
Azimilide (NE-10064) dihydrochloride is a class III antiarrhythmic agent, which works by blocking potassium channels in the heart. Azimilide dihydrochloride is a dual blocker of IKs (IC50 = 2.6 μM (2mM [K⁺]ₑ)) and IKr (IC50 = 1 μM (4 mM [K⁺])). Azimilide dihydrochloride blocked HERG channel at 0.1 and 1 Hz with IC50s of 1.4 μM and 5.2 μM respectively. Azimilide dihydrochloride also inhibits L-type calcium current (ICa) (IC50 = 17.8 μM) and sodium current (INa) (IC50 = 19 μM). Azimilide dihydrochloride can be used for the study of atrial fibrillation and ventricular fibrillation .
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2
2 Cited Publications
Cat. No.: HY-18600
CAS No.: 149908-53-2
Synonyms: NE-10064
Azimilide (NE-10064) is a class III antiarrhythmic agent, which works by blocking potassium channels in the heart. Azimilide is a dual blocker of IKs (IC50 = 2.6 μM (2mM [K⁺]ₑ)) and IKr (IC50 = 1 μM (4 mM [K⁺])). Azimilide blocked HERG channel at 0.1 and 1 Hz with IC50s of 1.4 μM and 5.2 μM respectively. Azimilide also inhibits L-type calcium current (ICa) (IC50 = 17.8 μM) and sodium current (INa) (IC50 = 19 μM). Azimilide can be used for the study of atrial fibrillation and ventricular fibrillation .
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1
1 Cited Publications
Cat. No.: HY-108575
CAS No.: 163163-23-3
Purity:  99.2%
Target:  

Potassium Channel CFTR

Research Areas:  

Cardiovascular Disease

Chromanol 293B is a selective blocker of the slow delayed rectifier K + current (IKs) with IC50 of 1-10 μM and a weak inhibitor of KATP channel. Chromanol 293B also blocks the CFTR chloride current with an IC50 of 19 μM .
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1
1 Cited Publications
Cat. No.: HY-16953
CAS No.: 878489-28-2
JNJ-303 is a specific delayed rectifier Kv blocker. JNJ 303 can potent block IKs with an IC50 value of 64 nM. JNJ-303 can be used for the research of diabetes, obesity and central nervous system .
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Cat. No.: HY-108591
CAS No.: 103342-82-1
Purity:  99.67%
Synonyms: R-L3
Target:  

Potassium Channel

Research Areas:  

Cardiovascular Disease

L-364,373 (R-L3) is a voltage-gated Kv7.1 (KCNQ1)/mink channels activator. L-364,373 activates Iks (slow delayed rectifier potassium current) and shortens action potential duration in guinea pig cardiac myocytes, and suppresses early afterdepolarizations in rabbit ventricular myocytes .
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Cat. No.: HY-106577
CAS No.: 53267-01-9
Purity:  95.08%
Synonyms: Cifenline; Ro 22-7796
Cibenzoline is a class Ia antiarrhythmic active molecule with low anticholinergic activity. Cibenzoline is a KATP channel inhibitor, acting through the pore forming subunit Kir6.2, with an IC50 of 22.2 μM. Cibenzoline inhibits IKr and IKs currents with IC50 values of 8.8 μM and 12.3 μM, respectively. Cibenzoline is used in the study of cardiac diseases. In addition, Cibenzoline can induce hypoglycemia .
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Cat. No.: HY-121977
CAS No.: 199335-15-4
Target:  

Potassium Channel

Research Areas:  

Inflammation/Immunology

IKs124 is KCNE2/KCNQ1 potassium channel blocker with the with an IC50 of 8 nM. IKs124 can be used for study of peptic ulcers .
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Cat. No.: HY-120141
CAS No.: 177954-68-6
Target:  

Potassium Channel

Research Areas:  

Cardiovascular Disease

L-768673 is a potent selective IKs blocker with antiarrhythmic effects. L-768673 plays important roles in both atrial and ventricular refractoriness as well as pacemaker function in the dog heart. L-768673 can be used for arrhythmias research .
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Cat. No.: HY-117174
CAS No.: 170228-29-2
Target:  

Potassium Channel

Research Areas:  

Cardiovascular Disease

L-735821 is a Potassium channel blocker and an antagonist of IKs. L-735821 inhibits the KCNQ1 channel activity with an EC50 of 0.08 μM. L-735821 can increase IKs and IKr current-voltage relations in rabbit ventricular myocytes. L-735821 fully abolishes IKs in isolated human ventricular myocytes at 100 nmol/L. L-735821 can easily enter single myocytes .
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Cat. No.: HY-P990978
CAS No.: 2930815-95-3
Synonyms: FS-1502 Antibody; IKs-014 Antibody

Target:  

EGFR

Research Areas:  

Inflammation/Immunology

HY-P990978 is an ERBB2-targeting IgG1κ type humanized antibody, the recommed isotype control is Human IgG1 kappa, Isotype Control (HY-P99001) .
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Cat. No.: HY-N15937
CAS No.: 2707415-27-6
Research Areas:  

Others

IKS02, a phosphatidylcholine (PC) phospholipid, is a photoaffinity labeling (PAL) probe .
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Cat. No.: HY-121520
CAS No.: 132850-40-9
Docosahexaenoyl glycine is a PUFA analogue. Docosahexaenoyl glycine has activating effects on IKs channels and restore the function of IKs channels with LQT1 mutation .
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Cat. No.: HY-18600B
CAS No.: 1294552-65-0
Synonyms: (E)-NE-10064
Target:  

Potassium Channel

Research Areas:  

Cardiovascular Disease

(E)-Azimilide is an isomer of Azimilide (HY-18600), a class of antiarrhythmic compounds that inhibit I(Ks) and I(Kr) activity .
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Cat. No.: HY-P992003
Synonyms: IKs01 Antibody

Target:  

ADC Antibodies

Research Areas:  

Cancer

IKS012 (IKS01) Antibody is a monoclonal antibody inhibitor targeting folate receptor α (FRA). IKS012 Antibody can be used to synthesize the antibody-drug conjugate (ADC) IKS012. IKS012 Antibody can be used to research related to platinum-resistant ovarian cancer .
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Cat. No.: HY-110015
CAS No.: 163163-24-4
Target:  

Potassium Channel

Research Areas:  

Cardiovascular Disease

(-)-Chromanol 293B is a potent and selective inhibitor of the slow component of delayed rectifier K + current (IKs). (-)-Chromanol 293B can be used for the research of antiarrhythmic .
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Cat. No.: HY-106577R
CAS No.: 53267-01-9
Synonyms: Cifenline (Standard); Ro 22-7796 (Standard)
Cibenzoline (Standard) is the analytical standard of Cibenzoline. This product is intended for research and analytical applications. Cibenzoline is a class Ia antiarrhythmic active molecule with low anticholinergic activity. Cibenzoline is a KATP channel inhibitor, acting through the pore forming subunit Kir6.2, with an IC50 of 22.2 μM. Cibenzoline inhibits IKr and IKs currents with IC50 values of 8.8 μM and 12.3 μM, respectively. Cibenzoline is used in the study of cardiac diseases. In addition, Cibenzoline can induce hypoglycemia .
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Cat. No.: HY-106577S
Synonyms: Cifenline-d4; Ro 22-7796-d4
Cibenzoline-d4 (Cifenline-d4) is deuterium labeled Cibenzoline. Cibenzoline is a class Ia antiarrhythmic active molecule with low anticholinergic activity. Cibenzoline is a KATP channel inhibitor, acting through the pore forming subunit Kir6.2, with an IC50 of 22.2 μM. Cibenzoline inhibits IKr and IKs currents with IC50 values of 8.8 μM and 12.3 μM, respectively. Cibenzoline is used in the study of cardiac diseases. In addition, Cibenzoline can induce hypoglycemia .
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Cat. No.: HY-P991899
Synonyms: LCB73 Antibody

Target:  

ADC Antibodies CD19

Research Areas:  

Cancer

IKS03 Antibody (LCB73 Antibody) is an anti-human CD19 antibody. IKS03 Antibody can generate antibody drug conjugate (ADC) (IKS03) with a pyrrolobenzodiazepine (PBD) dimer payload. IKS03 Antibody can be used for the study of diffuse large B-cell lymphoma (DLBCL) and mantle cell lymphoma (MCL) .
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Cat. No.: HY-18600AS
Synonyms: NE-10064-d8 dihydrochloride
Azimilide-d8 (NE-10064-d8) dihydrochloride is the deuterium labeled Azimilide dihydrochloride (HY-18600A). Azimilide dihydrochloride is a class III antiarrhythmic agent, which works by blocking potassium channels in the heart. Azimilide dihydrochloride is a dual blocker of IKs (IC50 = 2.6 μM (2mM [K⁺]ₑ)) and IKr (IC50 = 1 μM (4 mM [K⁺])). Azimilide dihydrochloride blocked HERG channel at 0.1 and 1 Hz with IC50s of 1.4 μM and 5.2 μM respectively. Azimilide dihydrochloride also inhibits L-type calcium current (ICa) (IC50 = 17.8 μM) and sodium current (INa) (IC50 = 19 μM). Azimilide dihydrochloride can be used for the study of atrial fibrillation and ventricular fibrillation .
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