5 Results for "

guinea-pig papillary muscle

" in MedChemExpress (MCE) Product Catalog:
Products (5)

5 Results for "guinea-pig papillary muscle" in MCE Product Catalog:

Cat. No.: HY-106831
CAS No.: 104606-13-5
Target:  

Calcium Channel

Research Areas:  

Cardiovascular Disease

R 56865 is a cardiomyocyte protective agent that protects against digitoxin (Ouabain)-induced myocardial calcium overload. R 56865 has a protective effect against digitoxin-induced intoxication in guinea pig papillary muscle .
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Cat. No.: HY-114920
CAS No.: 40680-87-3
Target:  

Calcium Channel

Research Areas:  

Cardiovascular Disease

Piprofurol is a calcium channel inhibitor. Piprofurol inhibits the calcium-induced contractions in isolated potassium depolarized preparations of rat aorta in a concentration-dependent manner and relaxes the K +-induced contraction of the dog coronary artery and the rabbit basilar artery. Piprofurol exerts a negative inotropic effect on guinea-pig papillary muscle, with the EC50 of 5 μM .
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Cat. No.: HY-136677
CAS No.: 118549-42-1
Target:  

Calcium Channel

Research Areas:  

Cardiovascular Disease

LND 796 is an aminosteroidal derivative with positive inotropic effects similar to those of digitalis. It exhibits electrophysiological, toxic, and inotropic effects in normal and partially potassium-depolarized ventricular muscles. LND 796 requires higher concentrations than digoxin to induce the same toxic symptoms. It exhibits a concentration-dependent positive inotropic effect on guinea pig papillary muscles in normal potassium solution. In partially potassium-depolarized papillary muscles, LND 796 enhances both components of contraction and increases the amplitude of slow action potentials. The mechanism of positive inotropic action of LND 796 involves enhanced calcium entry in calcium channels and inhibition of sodium-potassium ATPase. Due to its expanded positive inotropic range, LND 796 may have potential application in the treatment of congestive heart failure.
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Cat. No.: HY-184751
CAS No.: 58409-59-9
Research Areas:  

Cardiovascular Disease

Bucumolol is an orally active β-adrenergic receptor blocker. Bucumolol inhibits Renin release. Bucumolol exhibits activities including local anesthesia, antiarrhythmia, antihypertension, heart rate reduction, negative inotropy, cardiac action potential inhibition, and action potential duration shortening. Bucumolol does not increase cardiac electrical threshold, prolong atrial refractory period, or affect body weight in rodents. Bucumolol can be used in research related to arrhythmia and hypertension .
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Cat. No.: HY-106501A
CAS No.: 91574-89-9
Synonyms: Goe 4704 hydrochloride
Target:  

Potassium Channel

Research Areas:  

Cardiovascular Disease

Asocainol hydrochloride (Goe 4704 hydrochloride) is an antiarrhythmic agent. Asocainol hydrochloride reduces the maximum rate of action potential rise and action potential amplitude. Asocainol hydrochloride is applicable for the research of arrhythmias .
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