| 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. |
| M58553 | Indoramin | Indoramin is a selective α1A-adrenoceptor antagonist. |
| M58501 | Phentolamine | Phentolamine is a potent, selective and orally active α1 adrenergic and α2 adrenergic receptor antagonist. |
| M55510 | Clenbuterol-d9 | Clenbuterol-d9 |
| 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. |
| M30669 | Naphazoline | Naphazoline (Naphthazoline) is a potent α-adrenergic receptor agonist. Naphazoline reduces vascular hyperpermeability and promotes vasoconstriction. Naphazoline reduces the levels of inflammatory factors (TNF-α, IL-1β and IL-6), cytokines (IFN-γ and IL-4), IgE, GMCSF, and NGF。Naphazoline can be used for non-bacterial conjunctivitis research. |
| 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. |
| 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. |
| M20993 | S(-)-Propranolol hydrochloride | (S)-(-)-Propranolol hydrochloride, the active enantiomer of propranolol, is a β-Adrenoceptor (β-Adrenergic Receptor) antagonist with log Kd values of -8.16, -9.08, and -6.93 for β1, β2, and β3, respectively. |
| 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. |
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