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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.
M5895 Prazosin hydrochloride Prazosin hydrochloride, a Quinazoline derivative, is a well-tolerated, CNS-active α1-adrenergic receptor antagonist for the research of high blood pressure and alcohol use disorders.
M5894 Prazosin Prazosin is a well-tolerated, CNS-active α1-adrenergic receptor antagonist for the research of high blood pressure and alcohol use disorders.
M5822 Noradrenaline bitartrate monohydrate Noradrenaline bitartrate monohydrate is a direct alpha-adrenergic receptors stimulator.
M5785 Metoprolol Tartrate Metoprolol Tartrate is a selective β1 receptor blocker medication, used to treat hypertension and heart failure.
M5784 Metoprolol Succinate Metoprolol Succinate (Toprol XL) is a selective β1 receptor blocker used in treatment of several diseases of the cardiovascular system, especially hypertension.
M5781 Methoxyphenamine HCl Methoxyphenamine Hydrochloride is a β-adrenergic receptor agonist of the amphetamine class used as a bronchodilator.
M5774 Metaproterenol Sulfate Metaproterenol Sulfate(Orciprenaline Sulfate) is a direct acting sympathetic agonist. It is a β 2-adrenergic receptor (β2AR) agonist with an IC50 of 68 nM. It also has anti-inflammatory activity.
M5720 Ivabradine HCl Ivabradine HCl, a new If inhibitor with IC 50 of 2.9 μM which acts specifically on the pacemaker activity of the sinoatrial node, is a pure heart rate lowering agent.
M5685 Guanfacine HCl Guanfacine Hcl, an anti-hypertensive agent, is a selective α2A-adrenoceptor agonist with Kd of 31 nM and displays 60-fold selectivity over α2B-adrenoceptors.
M5644 Fenoterol hydrobromide Fenoterol hydrobromide is a β 2 adrenergic agonist designed to open up the airways to the lungs, is classed as sympathomimetic β2 agonist and asthma medication.
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.
M5477 Carbazochrome sodium sulfonate (AC-17) Carbazochrome sodium sulfonate (AC-17) is an antihemorrhagic for use in the treatment of hemorrhoids.
M5471 Buflomedil HCl Buflomedil HCl is a vasodilator used to treat claudication or the symptoms of peripheral arterial disease; A nonselective alpha adrenergic receptor inhibitor
M5462 Bisoprolol fumarate Bisoprolol fumarate is a selective type β1 adrenergic receptor blocker.
M5459 Atipamezole HCl Atipamezole is a synthetic α2 adrenergic receptor antagonist. It has also been researched in humans as a potential anti-Parkinsonian drug. Atipamezole hydrochloride is hydrochloride form of atipamezole.
M5456 B-HT 920 dihydrochloride B-HT 920(Talipexole 2Hcl) is a dopamine D2 receptor agonist, α2-adrenoceptor agonist and 5-HT3 receptor antagonist, which displays antiParkinsonian activity.
M5453 Betaxolol Betaxolol is a selective beta1-adrenergic receptor inhibitor that lowers intraocular pressure by reducing intraocular fluid production and may be used in studies related to hypertension and glaucoma.
M5429 Atipamezole Atipamezole is a synthetic α2 adrenergic receptor antagonist. It has also been researched in humans as a potential anti-Parkinsonian drug.
M5428 Atenolol Atenolol is a selective β1 receptor antagonist.
M5405 Amezinium methylsulfate Amezinium metilsulfate has multiple mechanisms, including stimulation of alpha and beta-1 receptors and inhibition ofnoradrenaline and tyramine uptake.




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