| 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. |
| M3411 | Sotalol | Sotalol is a non-selective beta blocker and a potassium channel blocker with an IC50 of 43 μM. |
| M3408 | Maprotiline hydrochloride | Maprotiline hydrochloride is a selective noradrenalin re-uptake inhibitor and a tetracyclic antidepressant. |
| M3372 | Clonidine hydrochloride | Clonidine hydrochloride is a direct-acting α2 adrenergic agonist with an ED50 of 0.02±0.01 mg/kg. |
| M3330 | Phenylephrine hydrochloride | Phenylephrine hydrochloride is a selective α1-adrenergic receptor agonist. |
| M3271 | Methyldopa | Methyldopa (Aldomet) is a DOPA decarboxylase competitive inhibitor with an ED50 of 21.8 mg/kg. |
| M3176 | Metaraminol bitartrate | Metaraminol bitartrate is an α-adrenoceptor agonist. |
| M3169 | Lofexidine hydrochloride | Lofexidine hydrochloride is an selective α2A-adrenergic receptor agonist. |
| M3076 | Tolazoline hydrochloride | Tolazoline is a non-selective competitive α-adrenergic receptor antagonist. |
| M3072 | Timolol Maleate | Timolol Maleate is a non-selective, beta-adrenergic receptor antagonist for β1/β2 with Ki of 1.97 nM/2.0 nM. |
| M3060 | Tetrahydrozoline hydrochloride | Tetrahydrozoline hydrochloride is an imidazoline derivative with alpha receptor agonist activity. |
| M3043 | Synephrine hydrochloride | SynephrineHCl (Oxedrine, p-Synephrine) is a sympathomimetic α-adrenergic receptor (AR) agonist. |
| M2973 | Ractopamine hydrochloride | Ractopamine hydrochloride (RAC), a beta-agonist with established nutrient partitioning capabilities, promotes skeletal muscle accretion at the expense of fat deposition. |
| M2964 | Propranolol hydrochloride | Propranolol hydrochloride is a competitive non-selective beta-adrenergic receptors inhibitor with IC50 of 12 nM. |
| M2907 | Oxprenolol hydrochloride | Oxprenolol hydrochloride is a non-selective beta blocker with some intrinsic sympathomimetic activity. |
| M2842 | Methoxamine hydrochloride | Methoxamine is an α1-adrenergic receptor agonist, it induces vasoconstriction of skin and splanchnic blood vessels. |
| M2834 | Medetomidine hydrochloride | Medetomidine is a selective α2-adrenoceptor agonist, with Ki of 1.08 nM, exhibts 1620-fold selectivity over α1-adrenoceptor. |
| M2809 | Levobetaxolol hydrochloride | Levobetaxolol exhibits a higher affinity at cloned human β1 and β2 receptors with Ki value of 0.76 nM and 32.6 nM, respectively. |
| M2808 | Levalbuterol hydrochloride | Levalbuterol HCl is a relatively selective beta2-adrenergic receptor agonist that may be used in asthma-related studies. |
| M2778 | Isoetharine Mesylate | Isoetharine is a selective beta2-adrenergic receptor agonist, which gives quick relief for bronchospasm and asthma. |
| M2772 | Indacaterol Maleate | Indacaterol is an ultra-long-acting β-adrenoceptor agonist with pKi of 7.36. |
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