341 Results for "

Antiarrhythmic

" in MedChemExpress (MCE) Product Catalog:
Products (341)

341 Results for "Antiarrhythmic" in MCE Product Catalog:

1
1 Cited Publications
Cat. No.: HY-33350
CAS No.: 92953-10-1
Research Areas:  

Cardiovascular Disease Cancer

Clofilium tosylate, a potassium channel blocker, induces apoptosis of human promyelocytic leukemia (HL-60) cells via Bcl-2-insensitive activation of caspase-3. Antiarrhythmic agent .
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1 Cited Publications
Cat. No.: HY-B1109
CAS No.: 32795-44-1
Synonyms: Acecainide; NAPA
Research Areas:  

Cardiovascular Disease

N-Acetylprocainamide is a class III antiarrhythmic, which blocks K + channels.
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1
1 Cited Publications
Cat. No.: HY-100572
CAS No.: 76252-06-7
Purity:  99.86%
Synonyms: RU-42924
Target:  

Sodium Channel

Research Areas:  

Cardiovascular Disease

Nicainoprol is a fast-sodium-channel blocking agent, which is a potent antiarrhythmic agent.
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1
1 Cited Publications
Cat. No.: HY-B0432B
CAS No.: 107381-32-8
Synonyms: (S)-SA-79
Target:  

Sodium Channel

Research Areas:  

Cardiovascular Disease

(S)-Propafenone ((S)-SA-79) is the S-enantiomer of Propafenone. (S)-Propafenone ((S)-SA-79) exerts beta-blocking action and the sodium channel-dependent antiarrhythmic class 1 activity .
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1 Cited Publications
Cat. No.: HY-135121
CAS No.: 57530-40-2
Purity:  98.45%
Synonyms: Ethacizin; NIK-244
Target:  

Sodium Channel

Research Areas:  

Cardiovascular Disease

Ethacizine hydrochloride (Ethacizin; NIK-244) is a longer-lasting Class Ic antiarrhythmic agent than Flecainide . Ethacizine hydrochloride (Ethacizin; NIK-244) inhibits the depolarizing current responsible for the intraatrial and His-Purkinje-ventricular conduction .
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1 Cited Publications
Cat. No.: HY-101433
CAS No.: 34118-92-8
Purity:  99.83%
Synonyms: Acecainide hydrochloride; NAPA hydrochloride
Research Areas:  

Cardiovascular Disease

N-Acetylprocainamide (Acecainide) hydrochloride is a class III antiarrhythmic, which blocks K + channels. N-Acetylprocainamide hydrochloride exerts inhibitory effects on the maximum following frequency (MFF) of isolated rabbit atria. N-Acetylprocainamide hydrochloride can be used for the study of arrhythmias .
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1 Cited Publications
Cat. No.: HY-A0082
CAS No.: 3254-89-5
Synonyms: Difenidol hydrochloride
Target:  

mAChR Sodium Channel

Research Areas:  

Neurological Disease

Diphenidol hydrochloride (Difenidol hydrochloride) is a non-selective muscarinic M1-M4 receptor antagonist, has anti-arrhythmic activity. Diphenidol hydrochloride is also a potent non-specific blocker of voltage-gated ion channels (Na +, K +, and Ca 2+) in neuronal cells. Diphenidol hydrochloride can be used in the study of antivertigo and antinausea .
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1
1 Cited Publications
Cat. No.: HY-106225
CAS No.: 355151-12-1
Purity:  99.50%
Synonyms: ZP123
Target:  

Gap Junction Protein

Research Areas:  

Cardiovascular Disease

Rotigaptide (ZP123) is a novel and specific modulator of connexin 43 (Cx43). Rotigaptide prevents the uncoupling of Cx43-mediated gap junction communication and normalizes cell-to-cell communication during acute metabolic stress. Rotigaptide is a potent antiarrhythmic peptide (AAP) with improved stability and has the potential for the investigation of cardiac arrhythmias-specifically atrial fibrillation .
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1 Cited Publications
Cat. No.: HY-120026
CAS No.: 147030-48-6
Purity:  98.28%
Synonyms: KB015
KB130015 (KB015) is an orally active and potent ThRα and ThRβ (thyroid hormone receptor) inhibitor, with IC50 values of 4.5 and 5.1 μM, respectively. KB130015 markedly slows the kinetics of inactivation of Na + channels. KB130015 activates hERG1 channels (EC50 = 12.2 μM) and large-conductance Ca 2+-activated K + (BKCa) channels formed by hSlo1 (α) subunits in HEK 293 cells. KB130015 has antiarrhythmic properties. KB130015 can be used for the study of cardiovascular disease .
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1 Cited Publications
Cat. No.: HY-B0551
CAS No.: 309-29-5
Target:  

Potassium Channel

Research Areas:  

Neurological Disease

Doxapram is a respiratory stimulant. Doxapram increases breathing rate and depth by acting on the brain's respiratory centers and peripheral chemoreceptors. Doxapram inhibits TASK-1, TASK-3, TASK-1/TASK-3 heterodimeric channel function with EC50s of 410 nM, 37 μM, 9 μM, respectively. Doxapram inhibits the Ca²⁺-activated potassium current (IC50 ≈ 13 μM) and Ca²⁺-independent potassium current (IC50 ≈ 20 μM) in type I cells of the carotid body. Doxapram significantly prolongs the effective refractory period of the atrium and has an anti-arrhythmic effect. Doxapram can be used for the study of respiratory depression such as post-anesthesia respiratory depression, chronic obstructive pulmonary disease and apnea of prematurity .
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1 Cited Publications
Cat. No.: HY-B0551A
CAS No.: 7081-53-0
Target:  

Potassium Channel

Research Areas:  

Neurological Disease

Doxapram hydrochloride hydrate is a respiratory stimulant. Doxapram hydrochloride hydrate increases breathing rate and depth by acting on the brain's respiratory centers and peripheral chemoreceptors. Doxapram hydrochloride hydrate inhibits TASK-1, TASK-3, TASK-1/TASK-3 heterodimeric channel function with EC50s of 410 nM, 37 μM, 9 μM, respectively. Doxapram hydrochloride hydrate inhibits the Ca²⁺-activated potassium current (IC50 ≈ 13 μM) and Ca²⁺-independent potassium current (IC50 ≈ 20 μM) in type I cells of the carotid body. Doxapram hydrochloride hydrate significantly prolongs the effective refractory period of the atrium and has an anti-arrhythmic effect. Doxapram hydrochloride hydrate can be used for the study of respiratory depression such as post-anesthesia respiratory depression, chronic obstructive pulmonary disease and apnea of prematurity .
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Cat. No.: HY-150123
CAS No.: 42982-87-6
Purity:  99.75%
Target:  

Drug Metabolite

Research Areas:  

Cardiovascular Disease

Quinidine methiodide is a metabolite of Quinidine. Quinidine is an antiarrhythmic agent .
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Cat. No.: HY-B0772A
CAS No.: 130656-51-8
Synonyms: MS-551
Target:  

Potassium Channel

Research Areas:  

Cardiovascular Disease

Nifekalant hydrochloride (MS-551), a class III antiarrhythmic agent, is a IKr potassium channel blocker with an IC50 of 10 µM. Nifekalant hydrochloride can be used for refractory ventricular tachyarrhythmias research .
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Cat. No.: HY-14834A
CAS No.: 478941-93-4
Purity:  99.31%
Synonyms: ATI-2042 tartrate
Budiodarone (ATI-2042) tartrate is a chemical analogue of Amiodarone (HY-14187) with balanced, multiple cardiac ion channel (potassium, sodium and calcium channels) inhibiting activity. Budiodarone tartrate is an antiarrhythmic agent .
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Cat. No.: HY-101723
CAS No.: 81329-71-7
Purity:  99.36%
Synonyms: BMY 40327; MJ 14030
Target:  

Drug Metabolite

Research Areas:  

Cardiovascular Disease

Modecainide is a major metabolite of Encainide, which is an antiarrhythmic agent.
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Cat. No.: HY-101245
CAS No.: 88069-49-2
Purity:  99.94%
Synonyms: SUN-1165; Pilzicainidehydrochloride
Target:  

Sodium Channel

Research Areas:  

Cardiovascular Disease

Pilsicainide hydrochloride (SUN-1165) is an orally active sodium channel blocker and potent class Ic antiarrhythmic agent .
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Cat. No.: HY-W802239
CAS No.: 39162-75-9
Target:  

Drug Derivative

Asparaginate calcium is a calcium 2+ salt of asparaginate and anion/zwitterion form of aspartic acid. Asparaginate calcium is a calcium supplement and an antiarrhythmic active substance. Asparaginate calcium can be used for the research of arrhythmia .
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Cat. No.: HY-106612
CAS No.: 90402-40-7
Purity:  98.07%
Synonyms: U-K52046; Albanoquil
Target:  

Adrenergic Receptor

Research Areas:  

Cardiovascular Disease

Abanoquil (U-K52046), an potent and selective α-1 adrenoceptor antagonist, is an anti-arrhythmic agent. Abanoquil can be used for erectile dysfunction research .
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Cat. No.: HY-10913
CAS No.: 943134-39-2
Synonyms: GAP-134; ZP 1609
Target:  

Gap Junction Protein

Research Areas:  

Cardiovascular Disease

Danegaptide (GAP-134) is a potent, selective and orally active gap-junction modifier with an antiarrhythmic effect .
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Cat. No.: HY-131987S
Ethacizine-d5 is the deuterium labeled Ethacizine (HY-131987). Ethacizine is an antiarrhythmic agent with inhibitory activity on sodium channels.
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