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Adrenergic Receptor Adrenergic Receptor

Cat.No.  Name Information
M2628 Dexmedetomidine Dexmedetomidine is a potent and highly selective α-2 adrenergic receptor agonist with sedative effects.
M3057 Terbutaline Sulfate Terbutaline Sulfate is a selective β2-adrenergic receptor agonist with IC50 of 53 nM.
M3752 Phentolamine Mesylate Phentolamine mesylate is an orally active, rapid-acting alpha-adrenergic receptor antagonist, for the treatment of men suffering from erectile dysfunction (ED).
M2420 Labetalol hydrochloride Labetalol hydrochloride is a dual antagonist for both selective alpha1-adrenergic and nonselective beta-adrenergic receptors.
M13893 Labetalol Labetalol (AH5158) is an orally active selective α1- and non-selective β-adrenergic receptors competitive antagonist.
M5593 Doxazosin Mesylate Doxazosin, a quinazoline-derivative, selectively antagonizes postsynaptic α1-adrenergic receptors, used in the treatment of high blood pressure and urinary retention associated with benign prostatic hyperplasia.
M5462 Bisoprolol fumarate Bisoprolol fumarate is a selective type β1 adrenergic receptor blocker.
M7848 ICI 118,551 hydrochloride ICI 118,551 hydrochloride is a highly selective β2-adrenoceptor antagonist, with Kis of 0.7, 49.5 and 611 nM for β2, β1 and β3 receptors, respectively.
M2738 Guanabenz Acetate Guanabenz Acetate is an selective agonist of α2a-adrenergic receptor, α2b-adrenergic receptor and α2c-adrenergic receptor with pEC50 of 8.25, 7.01 and ~5, respectively.
M2682 Esmolol hydrochloride Esmolol is a cardioselective beta adrenergic receptor blocker, used to control rapid heartbeats or abnormal heart rhythms.
M2672 Epinephrine hydrochloride Epinephrine hydrochloride is a hormone and a neurotransmitter.
M2657 Droxidopa Droxidopa is a psychoactive compound and acts as a procompound to the neurotransmitters norepinephrine (noradrenaline) and epinephrine (adrenaline).
M2533 Clorprenaline hydrochloride Clorprenaline hydrochloride is a β2-receptor agonist, it has a significant expansion of the bronchial effect.
M2468 Brimonidine Tartrate Brimonidine Tartrate is a highly selective α-adrenergic receptor antagonist with an EC50 of 0.45 nM for α2A adrenoreceptor, and has been used to study open-angle glaucoma or ocular hypertension.
M2370 Adrenalone hydrochloride Adrenalone is an adrenergic agonist used as a topical vasoconstrictor and hemostatic, mainly acts on alpha-1 adrenergic receptors.
M2365 Acebutolol hydrochloride Acebutolol is a β-adrenergic receptors antagonist used in the treatment of hypertension, angina pectoris and cardiac arrhythmias.
M2348 (R)-(+)-Atenolol (R)-(+)-Atenolol binds to but does not activate beta-adrenergic receptors thereby blocking the actions of endogenous or exogenous beta-adrenergic agonists.
M2160 Reboxetine mesylate Reboxetine mesylate is a potent and selective inhibitor of noradrenalin uptake (Ki values are 1.1, 129 and > 10000 nM for rat NET, SERT and DAT respectively).
M2077 Detomidine hydrochloride Detomidine hydrochloride is a nonnarcotic, synthetic alpha-2 adrenoreceptor agonist.
M2069 Mirabegron Mirabegron (YM178) is a potent and selective β(3)-adrenoceptor agonist with EC50 of 22.4 nM.
M1889 Tamsulosin hydrochloride Tamsulosin is a new, highly selective α1A-adrenoceptor antagonist.
M1567 Nadolol Nadolol
M1534 Metoprolol Metoprolol is a selective β1 receptor blocker used for acute myocardial infarction, heart failure, angina pectoris and mild to moderate hypertension.
M58543 Ro 363 hydrochloride Ro 363 hydrochloride is a potent and highly selective β1-adrenoceptor agonist. Ro 363 hydrochloride is also an effective inotropic stimulant. Ro 363 hydrochloride is a cardiovascular modulator that reduces diastolic blood pressure and pronounces increases in myocardial contractility.
M56799 Dipivefrin Dipivefrin is a potent adrenergic agonist.
M56143 HOKU-81 HOKU-81 (4-Hydroxytulobuterol) is one of the metabolites of Tulobuterol.
M56142 Imiloxan Imiloxan is a potent and selective alpha 2B-adrenoceptor antagonist.
M56141 A-123189  A-123189 is a selective and potent α1D antagonist with Kis of 0.312 and 0.17 for human α1D and rat α1D, respectively.




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