169 Results for "

contractility

" in MedChemExpress (MCE) Product Catalog:
Products (169)

169 Results for "contractility" in MCE Product Catalog:

Cat. No.: HY-101366
CAS No.: 107756-30-9
Purity:  ≥99.0%
Target:  

Adrenergic Receptor

Research Areas:  

Endocrinology

A-61603 is a selective α1A/α1a-adrenergic receptor agonist with Ki of 8.89 nM for rat submaxillary gland α1A, Ki of 30.5 nM for cloned bovine α1a. A-61603 potentiates Ca 2+ transients with EC50 of 6.9 nM. A-61603 stimulates phosphoinositide hydrolysis, induces contractile responses in vas deferens, prostate strips, and spleen strips, and exhibits low activity in aortic rings. A-61603 can be used for research on adrenergic function .
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Cat. No.: HY-B1233
CAS No.: 543-82-8
Synonyms: 2-Amino-6-methylheptane; 1,5-Dimethylhexylamine; 6-Methyl-2-heptylamine
Octodrine (2-Amino-6-methylheptane) is a central nervous stimulant that increases the uptake of dopamine and noradrenaline. Octodrine is found to increase the pain threshold, cardiac rate (positive chronotropic effect) and myocardial contractility (positive inotropic effect) .
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Cat. No.: HY-153977
CAS No.: 701224-63-7
Purity:  99.90%
Target:  

NADPH Oxidase

Research Areas:  

Cardiovascular Disease

GLX481304 is a specific inhibitor of Nox-2 and -4, with IC50s of 1.25 μM. GLX481304 suppresses ROS production in isolated mouse cardiomyocytes and improves cardiomyocyte contractility. GLX481304 can be used for research of ischemic injury to the heart .
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Cat. No.: HY-118960
CAS No.: 186180-83-6
Purity:  99.28%
Target:  

ATP Synthase

Research Areas:  

Cardiovascular Disease

BMS-199264 hydrochloride is an inhibitor of F1F0 ATP hydrolase (IC50=0.5 μM) without inhibitory effect on F1F0 ATP synthase. BMS-199264 hydrochloride selectively inhibits ATP decline during ischemia to reduces cardiac necrosis. BMS-199264 hydrochloride also enhances the recovery of contractile function following reperfusion .
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Cat. No.: HY-162345
CAS No.: 2851991-63-2
Target:  

Calcium Channel

Research Areas:  

Cardiovascular Disease

CK-963 is an activator for cardiac troponin (cTnC) with Ki of 11.5 μM. CK-963 exhibits activity in enhancing cardiac contractility in Sprague-Dawley rats .
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Cat. No.: HY-P10655
Research Areas:  

Cardiovascular Disease

Caloxin 1C2 is a specific PMCA (plasma-membrane Ca 2+-ATPases) inhibitor. Caloxin 1C2 is selective for PMCA4 over PMCA1, 2 and 3. The Ki values of Caloxin 1C2 are 2.3 μM for PMCA4 and 21 μM for PMCA1. Caloxin 1C2 dose not cause any significant effects on total Ca 2+ transfer. Caloxin 1C2 affects coronary contractility .
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Cat. No.: HY-B2155
CAS No.: 773092-05-0
Acotiamide monohydrochloride trihydrate is an orally active, selective and reversible acetylcholinesterase (AChE) inhibitor, with IC50 of 1.79 μM. Acotiamide monohydrochloride trihydrate can enhance gastric contractility and accelerate delayed gastric emptying. Acotiamide monohydrochloride trihydrate has the potential for the research of functional dyspepsia involving gastric motility dysfunction and intestinal inflammatory .
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Cat. No.: HY-103291
CAS No.: 126959-88-4
Purity:  99.96%
Sar-[D-Phe8]-des-Arg9-Bradykinin is a agonist of B1 receptor. Sar-[D-Phe8]-des-Arg9-Bradykinin selectively amplifies the contractile response when incubation with human recombinant interleukin-1 β (IL-1 β) in rabbit aortic rings .
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Cat. No.: HY-N9141
CAS No.: 2565-01-7
Nantenine is a serotonergic receptor antagonist. Nantenine selectively inhibits the contractile response of tissues to serotonin. Nantenine can be isolated from Nandina domestica .
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Cat. No.: HY-112071
CAS No.: 57526-81-5
Purity:  99.18%
Target:  

Adrenergic Receptor

Research Areas:  

Cardiovascular Disease

Prenalterol is a selective β1-adrenergic receptor agonist. Prenalterol has no effect on gut smooth muscle contractile activity. Prenalterol can be used for researching cardiovascular disease .
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Cat. No.: HY-108991
CAS No.: 96843-99-1
Synonyms: (-)-T-0509
Target:  

Adrenergic Receptor

Research Areas:  

Cardiovascular Disease

T-0509 ((-)-T-0509) is a selective full agonist of the β1 receptor. T-0509 activates the cAMP signaling pathway through the β1 receptor and enhances myocardial contractility .
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Cat. No.: HY-B1233A
CAS No.: 5984-59-8
Synonyms: 2-Amino-6-methylheptane hydrochloride; 1,5-Dimethylhexylamine hydrochloride; 6-Methyl-2-heptylamine hydrochloride
Target:  

Dopamine Receptor

Research Areas:  

Neurological Disease

Octodrine (2-Amino-6-methylheptane) is a central nervous activator that increases the uptake of dopamine and noradrenaline. Octodrine is found to increase the pain threshold, cardiac rate (positive chronotropic effect) and myocardial contractility (positive inotropic effect) .
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Cat. No.: HY-P4678
CAS No.: 2480-41-3
Target:  

Vasopressin Receptor

Research Areas:  

Neurological Disease

(Phe2,Orn8)-Oxytocin is a selective V1 vasopressin agonist. (Phe2,Orn8)-Oxytocin induces a sustained contractility of rabbit epididymis with EC50 value of 280 nM .
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Cat. No.: HY-121467A
CAS No.: 185104-11-4
Synonyms: Z-338; YM443
Acotiamide hydrochloride is an orally active, selective and reversible acetylcholinesterase (AChE) inhibitor, with an IC50 of 1.79 μM. Acotiamide hydrochloride can enhance gastric contractility and accelerate delayed gastric emptying. Acotiamide hydrochloride has the potential for the research of functional dyspepsia involving gastric motility dysfunction and intestinal inflammatory .
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Cat. No.: HY-123268
CAS No.: 74513-77-2
Target:  

Adrenergic Receptor

Research Areas:  

Cardiovascular Disease

Ro 363, an effective inotropic stimulant, is a potent and highly selective β1-adrenoceptor agonist. RO 363 is a cardiovascular modulator that reduces diastolic blood pressure and pronounces increases in myocardial contractility .
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Cat. No.: HY-106844
CAS No.: 120223-04-3
Purity:  99.59%
Research Areas:  

Cardiovascular Disease

EMD 53998 is a cardiotonic agent that increases myocardial contractility as an inhibitor for phosphodiesterase III (PDE III) and a calcium sensitizer. EMD 53998 increases myocardial contractility, reduces energy consumption and the risk of inducing arrhythmias .
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Cat. No.: HY-P3591
CAS No.: 83903-32-6
Target:  

Calcium Channel

Research Areas:  

Neurological Disease

YMRF-NH2 is a neuropeptide. YMRF-NH2 binds to FMRFa-R with an EC50 value of 31 nM .
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Cat. No.: HY-107645
CAS No.: 131780-48-8
Purity:  ≥99.0%
Target:  

mAChR

Research Areas:  

Neurological Disease

DAU 5884 hydrochloride is a potent muscarinic M3 receptor antagonist. DAU 5884 hydrochloride inhibits methacholine-dependent effects on cell proliferation and muscle contractility .
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Cat. No.: HY-P3618
Cortistatin-29 is a neuropeptide. Cortistatin-29 alleviates neuropathic pain. Cortistatin-29 binds all somatostatin (SS) receptor subtypes with high affinity and shows IC50 values of 2.8 nM, 7.1 nM, 0.2 nM, 3.0 nM, 13.7 nM for SSTR1, SSTR2, SSTR3, SSTR4, SSTR5, respectively. Cortistatin-29 shows anti-fibrotic effects .
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Cat. No.: HY-107610
CAS No.: 146662-42-2
Purity:  99.60%
Target:  

Leukotriene Receptor

Research Areas:  

Inflammation/Immunology

SR2640 (hydrochloride) is a potent and selective competitive leukotriene D4/leukotriene E4 antagonist. SR2640 can be used for researching the role of leukotrienes in human asthma .
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