25 Results for "

RYR2

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

25 Results for "RYR2" in MCE Product Catalog:

3
3 Cited Publications
Art. -Nr.: HY-W010950
CAS. Nr.: 54143-55-4
Forschungsgebiete:  

Cardiovascular Disease

Flecainide is an orally active antiarrhythmic agent. Flecainide can block sodium channels and inhibit calcium ion release mediated by the cardiac ryanodine receptor (RyR2). Flecainide can be used in the research of diseases such as catecholaminergic polymorphic ventricular tachycardia (CPVT) [2].
3
3 Cited Publications
Art. -Nr.: HY-W010950A
CAS. Nr.: 57415-44-8
Forschungsgebiete:  

Cardiovascular Disease

Flecainide hydrochloride is an orally active antiarrhythmic agent. Flecainide hydrochloride can block sodium channels and inhibit calcium ion release mediated by the cardiac ryanodine receptor (RyR2). Flecainide hydrochloride can be used in the research of diseases such as catecholaminergic polymorphic ventricular tachycardia (CPVT) [2] .
1
1 Cited Publications
Art. -Nr.: HY-15292
CAS. Nr.: 927871-76-9
Reinheit:  99.77%
Target:  

Calcium Channel

Forschungsgebiete:  

Cardiovascular Disease

S107 is an orally available, blood brain barrier-permeable compound, which stabilizes RyR2 channels by enhancing the binding of calstabin 2 to the mutant Ryr2-R2474S channel. S107 inhibits Ca 2+ leakage from the sarcoplasmic reticulum (SR) and prevents cardiac arrhythmias and raises the seizure threshold [2].
Art. -Nr.: HY-119850
CAS. Nr.: 865433-00-7
Reinheit:  99.83%
Synonyms: ARM036; S44121
Target:  

Calcium Channel

Forschungsgebiete:  

Cardiovascular Disease

Aladorian (ARM036; S44121) is a non-peptidic ryanodine receptor 2 (RyR2) stabilizer. Aladorian stabilizes RyR2 channels and rectifies abnormal Ca²⁺ handling in cardiomyocytes. Aladorian improves cardiomyocyte Ca²⁺ homeostasis independent of dystrophin restoration. Aladorian attenuates early cardiomyopathy and enhances left ventricular function in a canine muscular dystrophy model. Aladorian can be used for the research of heart failure, Duchenne muscular dystrophy-associated cardiomyopathy and muscular dystrophy [2] .
Art. -Nr.: HY-149662
CAS. Nr.: 2681302-83-8
Reinheit:  99.92%
Forschungsgebiete:  

Cardiovascular Disease

TMDJ-035 is a high-affinity, selective RyR2 inhibitor with an EC50 of 0.0130 μM. TMDJ-035 reduces RyR2 protein expression without affecting action potential-induced Ca 2+ transients. TMDJ-035 decreases ATP content and intracellular Ca 2+ levels. TMDJ-035 inhibits arrhythmias in a CPVT mouse model carrying mutant RyR2s. TMDJ-035 has no effect on electrocardiogram parameters or cardiac systolic function. TMDJ-035 exacerbates heart failure in mouse myocardial infarction models and hypoxic cardiomyocytes by altering cardiac function, causing tissue damage, promoting inflammatory infiltration, collagen deposition, and changes in Myosin heavy chain/actin expression. TMDJ-035 can be used in studies related to heart failure, catecholaminergic polymorphic ventricular tachycardia, and arrhythmias [2] .
Art. -Nr.: HY-N7491A
CAS. Nr.: 2056011-05-1
Target:  

Calcium Channel

Forschungsgebiete:  

Cancer

ent-(+)-verticilide is a potent and selective inhibitor of cardiac ryanodine receptor (RyR2) calcium release channels with antiarrhythmic activity. ent-(+)-verticilide inhibits RyR2-mediated diastolic Ca2+ leak and exhibits higher potency and a distinct mechanism of action compared with theDantrolene and Tetracaine. ent-(+)-verticilide is a useful tool to investigate the therapeutic potential of targeting RyR2 hyperactivity in heart and brain pathologies .
Art. -Nr.: HY-149779
CAS. Nr.: 3012675-16-7
Target:  

Calcium Channel

Forschungsgebiete:  

Cardiovascular Disease

RyR2 stabilizer-1 (compound 12a) is a potent RyR2 stabilizer and SERCA2a activator with EC50s of 2.7 μM for RyR2 and 383 nM for SERCA2. RyR2 stabilizer-1 inhibits Ca 2+ leakage from the SR RyR2 while promoting SERCA2 to pump Ca 2+ back to SR, which make RyR2 stabilizer-1 possible to prevent cardiac arrhythmias .
Art. -Nr.: HY-RS19951
Forschungsgebiete:  

Others

Ryr2 Mouse Pre-designed siRNA Set A contains three designed siRNAs for Ryr2 gene (Mouse), as well as a negative control, a positive control, and a FAM-labeled negative control.

Art. -Nr.: HY-RS26453
Forschungsgebiete:  

Others

Ryr2 Rat Pre-designed siRNA Set A contains three designed siRNAs for Ryr2 gene (Rat), as well as a negative control, a positive control, and a FAM-labeled negative control.

Art. -Nr.: HY-RS12369
Forschungsgebiete:  

Others

RYR2 Human Pre-designed siRNA Set A contains three designed siRNAs for RYR2 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

Art. -Nr.: HY-P5114A
Target:  

Calcium Channel

Forschungsgebiete:  

Others

Maurocalcine TFA is an agonist of ryanodine receptor (RyR) channel types 1, 2 and 3 with cellular permeability. Maurocalcine TFA induces [ 3H]ryanodine binding on RyR1 with an EC50 value of 2558 nM. Maurocalcine TFA exhibits a apparent affinity of 14 nM for RyR2. Maurocalcine TFA can be applied to in vivo cell tracking or other cell imaging techniques [2] .
Art. -Nr.: HY-103059
CAS. Nr.: 1479049-35-8
Reinheit:  99.62%
Target:  

Calcium Channel

Forschungsgebiete:  

Cardiovascular Disease

SOICR-IN-1 (compound 32) is a store-overload induced calcium release (SOICR) inhibitor with an IC50 value of 14.6 μM. SOICR-IN-1 can be used for the research of cardiac arrhythmias .
Art. -Nr.: HY-Z7733
CAS. Nr.: 72956-44-6
Synonyms: Desmethylcarvedilol; BM-14242
Target:  

Calcium Channel

Forschungsgebiete:  

Metabolic Disease

O-Desmethylcarvedilol (Desmethylcarvedilol) is an active metabolite of the non-selective β-adrenergic receptor (β-AR) antagonist Carvedilol (HY-B0006). O-Desmethylcarvedilol inhibits store-overload-induced calcium release in HEK293 cells expressing the ryanodine receptor 2 (RyR2) R4496C (RyR2 R4496C) mutation (IC50 = 7.62 µM). O-Desmethylcarvedilol reduces increases in heart rate and prevents decreases in diastolic blood pressure induced by Isoproterenol (HY-B0468) in conscious rabbits (ED50s = 32 and 5 µg/kg, respectively) [2].
Art. -Nr.: HY-W010950S
CAS. Nr.: 127413-31-4
Flecainide-d3 is the deuterium labeled Flecainide. Flecainide is an orally active antiarrhythmic agent. Flecainide can block sodium channels and inhibit calcium ion release mediated by the cardiac ryanodine receptor (RyR2). Flecainide can be used in the research of diseases such as catecholaminergic polymorphic ventricular tachycardia (CPVT) .
Art. -Nr.: HY-164631
CAS. Nr.: 714906-29-3
Target:  

Calcium Channel

Forschungsgebiete:  

Cardiovascular Disease

EL20 is a selective cardiac ryanodine receptor 2 (RyR2) inhibitor. EL20 inhibits diastolic Ca 2+ leakage from the sarcoplasmic reticulum, reducing delayed afterdepolarizations and triggered arrhythmias. EL20 is promising for research of cardiovascular diseases .
Art. -Nr.: HY-P5319
Target:  

Calcium Channel

Forschungsgebiete:  

Others

MCaE12A is a high-affinity modulator of RyR2 and increases RyR2 sensitivity to cytoplasmic calcium concentrations promoting channel opening. MCaE12A acts as an important tool for RyR2 structure-to-function studies as well as for manipulating Ca2+ homeostasis and dynamic of cardiac cell .
Art. -Nr.: HY-178344
Forschungsgebiete:  

Cardiovascular Disease

Multi-target kinase-IN-6 is a Multiple target kinase inhibitor. Multi-target kinase-IN-6 can inhibit cardiac RyR2- and NaV1.5-channels but stimulate SERCA2a pump activity. Multi-target kinase-IN-6 can be used for the research of cardiovascular disease, such as heart failure .
Art. -Nr.: HY-119850A
CAS. Nr.: 1233219-11-8
Synonyms: ARM036 sodium; S44121 sodium
Target:  

Calcium Channel

Forschungsgebiete:  

Cardiovascular Disease

Aladorian (ARM036; S44121) sodium is a non-peptidic ryanodine receptor 2 (RyR2) stabilizer. Aladorian sodium stabilizes RyR2 channels and rectifies abnormal Ca²⁺ handling in cardiomyocytes. Aladorian sodium improves cardiomyocyte Ca 2+ homeostasis independent of dystrophin restoration. Aladorian sodium attenuates early cardiomyopathy and enhances left ventricular function in a canine muscular dystrophy model. Aladorian sodium can be used for the research of heart failure, Duchenne muscular dystrophy-associated cardiomyopathy and muscular dystrophy [2] .
Art. -Nr.: HY-W010950AR
CAS. Nr.: 57415-44-8
Flecainide hydrochloride is an orally active antiarrhythmic agent. Flecainide hydrochloride can block sodium channels and inhibit calcium ion release mediated by the cardiac ryanodine receptor (RyR2). Flecainide hydrochloride can be used in the research of diseases such as catecholaminergic polymorphic ventricular tachycardia (CPVT) [2] .
Art. -Nr.: HY-166478S
CAS. Nr.: 1794817-24-5
Synonyms: Desmethylcarvedilol-d5; BM-14242-d5
O-Desmethyl carvedilol-d5 (Desmethylcarvedilol-d5) is deuterium labeled O-Desmethylcarvedilol. O-Desmethylcarvedilol (Desmethylcarvedilol) is an active metabolite of the non-selective β-adrenergic receptor (β-AR) antagonist Carvedilol (HY-B0006). O-Desmethylcarvedilol inhibits store-overload-induced calcium release in HEK293 cells expressing the ryanodine receptor 2 (RyR2) R4496C (RyR2 R4496C) mutation (IC50 = 7.62 μM). O-Desmethylcarvedilol reduces increases in heart rate and prevents decreases in diastolic blood pressure induced by Isoproterenol (HY-B0468) in conscious rabbits (ED50s = 32 and 5 μg/kg, respectively) [2].