17 Results for "

rabbit hearts

" in MedChemExpress (MCE) Product Catalog:
Products (17)

17 Results for "rabbit hearts" in MCE Product Catalog:

3
3 Cited Publications
Cat. No.: HY-101381
CAS No.: 102394-31-0
Pureté:  99.93%
Synonyms: AF-DX 116
Target:  

mAChR

Domaines de recherche:  

Neurological Disease Metabolic Disease

Otenzepad (AF-DX 116) is a selective and competitive M2 muscarinic acetylcholine receptor antagonist, with IC50 values of 640 nM and 386 nM for rabbit peripheral lung and rat heart, respectively .
loading...
    loading...
1
1 Cited Publications
Cat. No.: HY-108573
CAS No.: 60559-98-0
Pureté:  99.81%
Target:  

Potassium Channel

Domaines de recherche:  

Cardiovascular Disease

P-1075 is a potent activator of sulfonylurea receptor 2-associated ATP-sensitive potassium channels (SUR2-KIR6), with an EC50 value of 45 nM for SUR2B-KIR6 channel activation . P-1075 also P1075 opens mitochondrial K(ATP) channels and generates reactive oxygen species resulting in cardioprotection of rabbit hearts .
loading...
    loading...
1
1 Cited Publications
Cat. No.: HY-14304A
CAS No.: 38241-28-0
Pureté:  99.34%
Synonyms: MJ 9184 hydrochloride
Target:  

Adrenergic Receptor

Domaines de recherche:  

Cardiovascular Disease

Zinterol hydrochloride (MJ 9184 hydrochloride) is a potent and selective β2-adrenoceptor agonist . Zinterol hydrochloride increases ICa in a concentration-dependent manner with an EC50 of 2.2 nM . Zinterol hydrochloride induces ventricular arrhythmias in conscious heart failure rabbits .
loading...
    loading...
1
1 Cited Publications
Cat. No.: HY-103346
CAS No.: 220509-74-0
Pureté:  99.97%
Target:  

Caspase Apoptosis

Domaines de recherche:  

Cardiovascular Disease

MMPSI is a potent and selective small molecule caspase 3 and caspase 7 inhibitor with an IC50 of 1.7 μM for human caspase-3. MMPSI can significantly reduce ischemia-reperfusion-induced infarct size in the isolated rabbit heart, and reduce apoptosis in both the ischemic myocardium and isolated cardiomyocytes. MMPSI can be used for researching cardioprotection .
loading...
    loading...
Cat. No.: HY-P3765
CAS No.: 91421-87-3
Target:  

Inhibitory Antibodies

Domaines de recherche:  

Cardiovascular Disease

Auriculin A is a synthetic atrial natriuretic factor (ANF) with hemodynamic effect. Auriculin A antagonizes renal vasoconstriction in the dog, and influences on arterial baroreflex control of heart rate, systemic blood pressure, and perfusion pressure in the hind limb (perfused at constant flow) in rabbits .
loading...
    loading...
Cat. No.: HY-Z7733
CAS No.: 72956-44-6
Synonyms: Desmethylcarvedilol; BM-14242
Target:  

Calcium Channel

Domaines de recherche:  

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) .
loading...
    loading...
Cat. No.: HY-N4080
CAS No.: 2241-90-9
Cyclobuxine D is a steroidal alkaloid extracted from Buxus microphylla. Cyclobuxine D has a significant bradycardic effect in the rat heart and an inhibitory action on acetylcholine and Ba ++−induced contraction of the longitudinal muscle isolated from the rabbit jejunum .
loading...
    loading...
Cat. No.: HY-P1440A
Target:  

Potassium Channel

Domaines de recherche:  

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.
loading...
    loading...
Cat. No.: HY-P1428A
Domaines de recherche:  

Cardiovascular Disease

RFRP-1(human) TFA is a potent endogenous NPFF receptor agonist (EC50 values are 0.0011 and 29 nM for NPFF2 and NPFF1, respectively). Attenuates contractile function of isolated rat and rabbit cardiac myocytes. Reduces heart rate, stroke volume, ejection fraction and cardiac output, and increases plasma prolactin levels in rats.
loading...
    loading...
Cat. No.: HY-108573R
CAS No.: 60559-98-0
Target:  

Potassium Channel

Domaines de recherche:  

Cardiovascular Disease

P-1075 (Standard) is the analytical standard of P-1075. This product is intended for research and analytical applications. P-1075 is a potent activator of sulfonylurea receptor 2-associated ATP-sensitive potassium channels (SUR2-KIR6), with an EC50 value of 45 nM for SUR2B-KIR6 channel activation . P-1075 also P1075 opens mitochondrial K(ATP) channels and generates reactive oxygen species resulting in cardioprotection of rabbit hearts .
loading...
    loading...
Cat. No.: HY-166478S
CAS No.: 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) .
loading...
    loading...
Cat. No.: HY-15208A
CAS No.: 158751-64-5
Synonyms: HMR 1098 free base
Target:  

Others

Domaines de recherche:  

Others

Clamikalant (HMR 1098 free base) is a compound used to suppress cardiac arrhythmias. It prevents the reduction of the refractory period during ventricular fibrillation in dogs and also shows antiarrhythmic effects in a rabbit heart model.
loading...
    loading...
Cat. No.: HY-180334
CAS No.: 120004-07-1
Target:  

Calcium Channel

Domaines de recherche:  

Cardiovascular Disease

S-312 is a calcium antagonist with a bicyclic dihydrothienopyridine structure. S-312 can relax the helical strips of various isolated rabbit arteries procontracted with high potassium depolarizaiton. S-312 competitively imhibits calcium-induced contractions in depolarized basilar and femoral arteries. S-312 increases AV nodal conduction time in Langenedorff-perfused isolated rabbit hearts. S-312 exhibits vasculoselectivity, particularly for cerebral vessel .
loading...
    loading...
Cat. No.: HY-189366
Domaines de recherche:  

Cardiovascular Disease

Antiarrhythmic agent-4 is an orally active cardiac ion channel modulator. Antiarrhythmic agent-4 selectively inhibits pathological late sodium current of the cardiac NaV1.5 channel (IC50 = 2.5 μM) while blocking the hERG (IKr) channel (IC50 = 1.5 μM). Antiarrhythmic agent-4 reduces intracellular sodium/calcium overload, prolongs the cardiac action potential, and avoids conduction block and negative inotropic effects. Antiarrhythmic agent-4 exhibits antiarrhythmic efficacy in an isoproterenol-induced atrial fibrillation model in isolated rabbit hearts and improves survival and cardiac function in a Doxorubicin (HY-15142A)-induced heart failure mouse model. Antiarrhythmic agent-4 can be used for research on atrial fibrillation and heart failure .
loading...
    loading...
Cat. No.: HY-103346R
CAS No.: 220509-74-0
Domaines de recherche:  

Cardiovascular Disease

MMPSI (Standard) is the analytical standard of MMPSI (HY-103346). This product is intended for research and analytical applications. MMPSI is a potent and selective small molecule caspase 3 and caspase 7 inhibitor with an IC50 of 1.7 μM for human caspase-3. MMPSI can significantly reduce ischemia-reperfusion-induced infarct size in the isolated rabbit heart, and reduce apoptosis in both the ischemic myocardium and isolated cardiomyocytes. MMPSI can be used for researching cardioprotection .
loading...
    loading...
Cat. No.: HY-123939
CAS No.: 1400687-19-5
Target:  

JAK ROCK

Domaines de recherche:  

Cardiovascular Disease

JAK1/3-IN-1 is a selective, orally active JAK1/3 inhibitor with IC50 values of 1.9 nM and 0.9 nM, respectively. JAK1/3-IN-1 significantly reduces the mean arterial blood pressure and significantly increases the heart rate in rabbits. JAK1/3-IN-1 decreases the mean arterial blood pressure in conscious telemetered rats and induces lethal cardiovascular effects .
loading...
    loading...
Cat. No.: HY-N16733
CAS No.: 4589-95-1
Deacetyltanghinin is a selective inhibitor targeting Na +/K + ATPase, acting through non-covalent binding but is highly cardiotoxic. Deacetyltanghinin inhibits Na +/K + ATPase activity, induces cancer cell apoptosis (involving caspase pathway activation), and at the same time affect the TXA2-PGI2 balance in the rabbit heart. Deacetyltanghinin has significant anti-cancer activity and is mainly used in the research field of targeted therapy of malignant tumors such as breast cancer and lung cancer. At the same time, attention should be paid to the regulation of its cardiotoxicity .
loading...
    loading...
  • 1