| Cat.No. | Name | Information |
|---|---|---|
| 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). |
| M3057 | Terbutaline Sulfate | Terbutaline Sulfate is a selective β2-adrenergic receptor agonist with IC50 of 53 nM. |
| M2628 | Dexmedetomidine | Dexmedetomidine is a potent and highly selective α-2 adrenergic receptor agonist with sedative effects. |
| M49460 | Apraclonidine hydrochloride | Apraclonidine hydrochloride is a selective α2 and weak α1 receptor agonist that reduces intraocular fluid production and increases drainage, and may be used in studies related to glaucoma. |
| M45196 | N-Methyltyramine | N-Methyltyramine is a proto-alkaloid that can be isolated from a variety of plants. N-Methyltyramine is also an α2-adrenergic receptor antagonist and enhances appetite and food digestion by stimulating gastrin and pancreatic secretion. In addition, N-Methyltyramine relaxes small intestinal smooth muscle and inhibits peristalsis in mice. |
| M40635 | DL-Norepinephrine hydrochloride | DL-Norepinephrine hydrochloride is a synthetic phenylephrine that mimics the sympathomimetic effects of endogenous norepinephrine and is also a neurotransmitter targeting the adrenergic receptors α1 and β1, which have been shown to lower the subendocardial partial pressure of oxygen. |
| M29764 | Timolol | Timolol is a beta receptor blocker that can be used in studies related to glaucoma and hypertension. |
| M25455 | Butoxamine hydrochloride | Butoxamine hydrochloride is a specific β2-adrenergic receptor blocker. |
| M22441 | Formoterol | Formoterol |
| M21593 | Aaptamine | Aaptamine, an alkaloid isolated from sponge Aaptos aaptos in the ocean, is a competitive antagonist of alpha-adrenergic receptors to activate the p21 promoter independently of the p53 pathway. |
| M20935 | Isoxsuprine hydrochloride | Isoxsuprine hydrochloride is a beta-adrenergic agonist with vasodilatory activity and may be used in studies related to preterm labor. |
| M20474 | Rauwolscine hydrochloride | Rauwolscine hydrochloride is the hydrochloride salt form of Rauwolscine, a specific and potent α2 antagonist with Ki of 12 nM. |
| M19193 | Higenamine | Higenamine is a β2-AR agonist, used in the research of heart failure. Higenamine (Norcoclaurine) has anti-apoptotic effects. |
| M16068 | α-Yohimbine | α-Yohimbine |
| M16031 | Tetrahydroalstonine | Tetrahydroalstonine is a selective alpha 2-adrenoceptor antagonist. |
| M13902 | Yohimbine | Yohimbine is a potent and relatively nonselective alpha 2-adrenergic receptor (AR) antagonist, with IC50 of 0.6 μM. |
| M13899 | SR59230A hydrochloride | SR59230A hydrochloride is a potent, selective, and blood-brain barrier penetrating β3-adrenergic receptor antagonist with IC50s of 40, 408, and 648 nM for β3, β1, and β2 receptors, respectively. |
| M13897 | Olodaterol hydrochloride | Olodaterol (BI1744) hydrochloride is a selective, long acting β2-adrenoceptor (β2-AR) agonist (EC50=0.1 nM and pKi= 9.14 for human β2-adrenoceptor, respectively). |
| M13894 | L-Epinephrine | L-Epinephrine is a hormone secreted by the medulla of the adrenal glands. L-Epinephrine is an α-adrenergic and β-adrenergic receptor agonist. |
| M13893 | Labetalol | Labetalol (AH5158) is an orally active selective α1- and non-selective β-adrenergic receptors competitive antagonist. |
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