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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.
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.
M7743 Dobutamine hydrochloride Dobutamine hydrochloride is a selective β1-AR agonist.
M7715 Clenbuterol hydrochloride Clenbuterol (NAB-365) hydrochloride is a selective β2-adrenergic agonist, bronchodilator, enhances skeletal muscle strength and hypertrophy. Clenbuterol hydrochloride induces growth factor mRNA, activates astrocytes, and protects rat brain tissue against ischemic damage.
M7702 CGP-20712A methanesulfonate salt CGP-20712A methanesulfonate salt is a selective β1-adrenoceptor antagonist with IC50 of 0.7 nM.
M7583 Oxprenolol Oxprenolol is a non-selective beta blocker with some intrinsic sympathomimetic activity.
M6887 L755507 L755507 is a potent, selective agonist of β3-AR with an IC50 of 35 nM. L755507 enhances the homology-directed repair (HDR)-mediated genome editing in CRISPR/Cas9 nickase system.
M6851 JP 1302 dihydrochloride JP1302 dihydrochloride is a potent, selective, high affinity antagonist of the α2C-adrenoceptor, with a Kb of 16 nM and a Ki of 28 nM for the human α2C-receptor.
M6613 CL 316243 disodium salt CL 316243 disodium salt is a highly selective β3 agonist. CL316243 is a effective stimulant of adipocyte lipolysis and increases brown adipose tissue thermogenesis and metabolic rate.
M6532 BRL 44408 maleate BRL 44408 maleate is a selective α2A antagonist.
M6461 Arformoterol tartrate Arformoterol tartrate is a long-acting β 2 agonist (LABA).
M6369 A 61603 hydrobromide A 61603 hydrobromide is a α 1A agonist.
M6326 2-MPMDQ 2-MPMDQ is a potent, selective α 1 antagonist. Also σ 2 ligand.
M6019 Tizanidine HCl Tizanidine hydrochloride is an α2-adrenergic receptor agonist and inhibits neurotransmitter release from CNS noradrenergic neurons.
M6000 Terazosin HCl Terazosin is a selective alpha-1 antagonist used for treatment of symptoms of an enlarged prostate (BPH). It works by blocking the action of adrenaline on smooth muscle of the bladder and the blood vessel walls.
M5999 Terazosin hydrochloride dihydrate Terazosin hydrochloride dihydrate is a selective, competitive and orally active α1-adrenoceptor antagonist. Terazosin is also an agonist of HSP90. Terazosin hydrochloride dihydrate can be used for the research of benign prostatic hyperplasia (BPH) and high blood pressure.
M5998 Terazosin Terazosin is a selective alpha1-antagonist used for treatment of symptoms of benign prostatic hyperplasia (BPH).
M5988 Tamsulosin Tamsulosin is a selective α1 receptor antagonist.
M5953 Scopine HCl Scopine Hcl salt is the metabolite of anisodine, which is a α1-adrenergic receptor agonist and used in the treatment of acute circulatory shock.
M5947 Salmeterol Xinafoate Salmeterol Xinafoate is a long-acting β2-adrenergic receptor agonist with anti-inflammatory effects, which is used to study asthma symptoms and COPD symptoms.
M5936 Ritodrine HCl Ritodrine HCl is a hydrochloride salt of ritodrine which is a β-2 adrenergic receptor agonist.




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