About 30 results found for searched term "Adrenergic Receptor" (0.06 seconds)
Cat.No. | Name | Target |
---|---|---|
M2348 | (R)-(+)-Atenolol | Adrenergic Receptor |
(R)-(+)-Atenolol binds to but does not activate beta-adrenergic receptors thereby blocking the actions of endogenous or exogenous beta-adrenergic agonists. | ||
M2365 | Acebutolol hydrochloride | Adrenergic Receptor |
Acebutolol is a β-adrenergic receptors antagonist used in the treatment of hypertension, angina pectoris and cardiac arrhythmias. | ||
M2370 | Adrenalone hydrochloride | Adrenergic Receptor |
Adrenalone is an adrenergic agonist used as a topical vasoconstrictor and hemostatic, mainly acts on alpha-1 adrenergic receptors. | ||
M2420 | Labetalol hydrochloride | Adrenergic Receptor |
Labetalol HCl | ||
Labetalol hydrochloride is a dual antagonist for both selective alpha1-adrenergic and nonselective beta-adrenergic receptors. | ||
M2468 | Brimonidine Tartrate | Adrenergic Receptor |
Brimonidine tartrate; AGN190342 tartrate; UK14304 tartrate | ||
Brimonidine Tartrate is a highly selective α-adrenergic receptor antagonist with an EC50 of 0.45 nM for α2A adrenoreceptor, and has been used to study open-angle glaucoma or ocular hypertension. | ||
M2628 | Dexmedetomidine | Adrenergic Receptor |
Dexmedetomidine is a potent and highly selective α-2 adrenergic receptor agonist with sedative effects. | ||
M2682 | Esmolol hydrochloride | Adrenergic Receptor |
Esmolol is a cardioselective beta adrenergic receptor blocker, used to control rapid heartbeats or abnormal heart rhythms. | ||
M2738 | Guanabenz Acetate | Adrenergic Receptor |
WY-8678 Acetate; GBZ Acetate; BR-750 | ||
Guanabenz Acetate is an selective agonist of α2a-adrenergic receptor, α2b-adrenergic receptor and α2c-adrenergic receptor with pEC50 of 8.25, 7.01 and ~5, respectively. | ||
M2778 | Isoetharine Mesylate | Adrenergic Receptor |
Isoetharine is a selective beta2-adrenergic receptor agonist, which gives quick relief for bronchospasm and asthma. | ||
M2808 | Levalbuterol hydrochloride | Adrenergic Receptor |
Levalbuterol HCl is a relatively selective beta2-adrenergic receptor agonist that may be used in asthma-related studies. | ||
M2842 | Methoxamine hydrochloride | Adrenergic Receptor |
Vasoxine HCl | ||
Methoxamine is an α1-adrenergic receptor agonist, it induces vasoconstriction of skin and splanchnic blood vessels. | ||
M2964 | Propranolol hydrochloride | Adrenergic Receptor |
Propranolol hydrochloride is a competitive non-selective beta-adrenergic receptors inhibitor with IC50 of 12 nM. | ||
M3043 | Synephrine hydrochloride | Adrenergic Receptor |
Oxedrine hydrochloride | ||
SynephrineHCl (Oxedrine, p-Synephrine) is a sympathomimetic α-adrenergic receptor (AR) agonist. | ||
M3057 | Terbutaline Sulfate | Adrenergic Receptor |
Terbutaline hemisulfate | ||
Terbutaline Sulfate is a selective β2-adrenergic receptor agonist with IC50 of 53 nM. | ||
M3072 | Timolol Maleate | Adrenergic Receptor |
(S)-Timolol Maleate; L-714465 Maleate; MK 950 | ||
Timolol Maleate is a non-selective, beta-adrenergic receptor antagonist for β1/β2 with Ki of 1.97 nM/2.0 nM. | ||
M3076 | Tolazoline hydrochloride | Adrenergic Receptor |
Imidaline hydrochloride; Benzidazol hydrochloride | ||
Tolazoline is a non-selective competitive α-adrenergic receptor antagonist. | ||
M3166 | Pindolol | 5-HT Receptor |
Pindolol is a nonselective beta blocker with partial beta-adrenergic receptor agonist activity. | ||
M3169 | Lofexidine hydrochloride | Adrenergic Receptor |
Baq-168; MDL-14042 | ||
Lofexidine hydrochloride is an selective α2A-adrenergic receptor agonist. | ||
M3330 | Phenylephrine hydrochloride | Adrenergic Receptor |
Phenylephrine hydrochloride is a selective α1-adrenergic receptor agonist. | ||
M3457 | Naftopidil | Adrenergic Receptor |
KT-611; BM-15275 | ||
Naftopidil is a selective α1-adrenergic receptor antagonist or alpha blocker with a Ki of 58.3 nM. | ||
M3605 | Salbutamol hemisulfate | Adrenergic Receptor |
Albuterol hemisulfate; AH-3365 hemisulfate | ||
Salbutamol hemisulfate is a short-acting β2-adrenergic receptor agonist with an IC50 of 8.93 µM. | ||
M3662 | Bambuterol hydrochloride | Adrenergic Receptor |
KWD-2183 | ||
Bambuterol hydrochloride is an effective β -adrenergic receptor agonist. | ||
M3675 | Rotigotine | Dopamine Receptor |
N-0923; (-)-N 0437 | ||
Rotigotine is a potent dopamine receptor agonist with Ki values of 0.71 nM, 4-15 nM, and 83 nM for the dopamine D3 receptor and D2, D5, D4 receptors and dopamine D1 receptor. Rotigotine a partial agonist of the 5-HT1A receptor, and an antagonist of the α2B-adrenergic receptor. | ||
M3752 | Phentolamine Mesylate | Adrenergic Receptor |
Phentolamine methanesulfonate; PHE Mesylate | ||
Phentolamine mesylate is an orally active, rapid-acting alpha-adrenergic receptor antagonist, for the treatment of men suffering from erectile dysfunction (ED). | ||
M3818 | Rotigotine Hydrochloride | Dopamine Receptor |
Rotigotine HCl;N-0923 Hydrochloride | ||
Rotigotine Hydrochloride (N-0923 Hydrochloride) is a full agonist of dopamine receptor, a partial agonist of the 5-HT1A receptor, and an antagonist of the α2B-adrenergic receptor, with Ki of 0.71 nM, 4-15 nM, and 83 nM for the dopamine D3 receptor and D2, D5, D4 receptors, and dopamine D1 receptor. | ||
M3967 | α-Hederin | Apoptosis |
Hed,alpha-hederin | ||
α-Hederin is a triterpene saponin which affects the binding behavior, dynamics, and regulation of beta 2-adrenergic receptors. | ||
M4447 | 3-Hydroxy-4-methoxycinnamic-acid | Adrenergic Receptor |
3-Hydroxy-4-methoxycinnamic acid | ||
Isoferulic acid (3-Hydroxy-4-methoxycinnamic acid) is a kind of cinnamic acid derivative with anti - diabetes activity. Isoferulic acid (3-hydroxy-4-methoxycinnamic acid) binds and activates α 1-adrenergic receptor (IC50=1.4 μM), Enhanced β -endorphin secretion (EC50=52.2 nM) and increased in vitro glucose use. Isoferulic acid also has activity against influenza virus. | ||
M4593 | Yohimbine-Hydrochloride | Adrenergic Receptor |
YHB Hydrochloride | ||
Yohimbine hydrochloride is an α2-adrenergic receptor antagonist. | ||
M5395 | Alfuzosin | Androgen Receptor |
SL 77499 | ||
Alfuzosin is an α1 adrenergic receptor antagonist used to treat benign prostatic hyperplasia (BPH). | ||
M5423 | Asenapine | 5-HT Receptor |
Org 5222 | ||
Asenapine(Org 5222) inhibits adrenergic receptor (α1, α2A, α2B, α2C) with Ki of 0.25-1.2 nM and also inhibits 5-HT receptor (1A, 1B, 2A, 2B, 2C, 5A, 6, 7) with Ki of 0.03-4.0 nM. |
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