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Adrenergic Receptor Isoform Specific Products
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Adrenergic Receptor Related Products (1649)
Related Products (1649)
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Antibodies (4)
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Adrenergic Receptor Isoform Comparison
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Etilefrine hydrochloride (Standard)
0 ImagesEtilefrine hydrochloride (Standard) is the analytical standard of Etilefrine hydrochloride (HY-A0144A). This product is intended for research and analytical applications. Etilefrine hydrochloride is a sympathetic nerve agonist and AMPK activator that selectively targets α1/β1 adrenergic receptors. Etilefrine hydrochloride stimulates α1 adrenergic receptors, leading to contraction of vascular smooth muscle and increased peripheral resistance. Etilefrine hydrochloride also stimulates β1 receptors to enhance myocardial contractility and increase heart rate, thereby increasing blood pressure and improving cardiac output. Etilefrine hydrochloride also bidirectionally regulates the AMPK/Akt pathway and modulates the phosphorylation levels. Etilefrine hydrochloride can be used in cardiovascular research, such as postural hypotension, chylothorax, and improving low cardiac output. -
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Bethanidine hydriodide
0 ImagesBethanidine hydriodide is an orally active antihypertensive agent and adrenergic neuron blocker. Bethanidine hydriodide exerts its antihypertensive effect by inhibiting the release of norepinephrine from sympathetic nerve terminals. Bethanidine hydriodide exhibits anti-ventricular arrhythmic activity. Bethanidine hydriodide can be used in research related to hypertension, ventricular tachycardia, and ventricular fibrillation. -
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Eclanamine maleate
0 ImagesCat. No.: HY-129862CAS No.: 67450-45-7Eclanamine maleate is an orally effective non-tricyclic antidepressant and an adrenergic receptor modulator. Eclanamine maleate blocks biogenic amine uptake and enhances α2-receptor sensitivity, and long-term administration induces downregulation and desensitization of cortical β-receptors. Eclanamine maleate is used in the study of depression. -
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CACPD2011a-0001278239
0 ImagesCat. No.: HY-168344CAS No.: 1030781-08-8CACPD2011a-0001278239 is a β2AR mixed agonist that shows a wide range of high-affinity binding to both wild-type and T164I β2AR variants, with no cytotoxicity or mutagenicity, making it suitable for asthma research. -
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Phenylethanolamine A-d3
0 ImagesCat. No.: HY-131103SCAS No.: 2507994-61-6Phenylethanolamine A-d3 is a deuterium labeled Phenylethanolamine A. Phenylethanolamine A acts as a β-adrenergic agonist. Phenylethanolamine A is a byproduct during the Ractopamine synthesis process. -
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Olmidine
0 ImagesCat. No.: HY-105718CAS No.: 31105-14-3Synonyms: DL-OlmidineOlmidine (DL-Olmidine) is an antihypertensive agent. Olmidine acts through inhibition of the adrenergic transmission. -
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Moprolol
0 ImagesMoprolol ((±)-Moprolol) is an beta-adrenergic receptor blocker, which can be used for research in essential hypertension. -
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NGD9002 free base
0 ImagesCat. No.: HY-118935CAS No.: 666256-06-0NGD9002 free base is a new generation of selective corticotropin-releasing factor-1 (CRF-1) receptor antagonist with inhibitory activity on CRF-induced colonic function stimulation. NGD9002 free base can reduce CRF-induced fecal output response and show an inhibitory IC50 value of 4.3 mg/kg. NGD9002 free base can effectively block CRF-induced colonic secretory motility stimulation at the highest dose and reduce acute water avoidance-induced defecation. NGD9002 free base can also prevent the occurrence of pain hypersensitivity reactions to repeated colonic distension. -
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CP-114271
0 ImagesCat. No.: HY-19277CAS No.: 162326-86-5CP-114271 is a potent selective β3-adrenergic receptor agonist. CP-114271 possesses an in vivo efficacy in rodent models. CP-114271 can be used for obesity research. -
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Desipramine
0 ImagesDesipramine is a first-generation tricyclic antidepressant. Desipramine selectively binds to norepinephrine transporter and blocks neuronal norepinephrine reuptake. Desipramine activates MAPK signaling via ERK1/2, JNK, and p38, represses NF-κB and AP-1 activity, and induces apoptosis via ROS elevation, mitochondrial membrane potential reduction, and intracellular calcium increase. Desipramine also shows anyi-inflammatory activity, inhibiting TNF-α production. Desipramine can be used for the research of hepatocellular cancer, inflammation, and neurological diseases. -
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Dextromilnacipran hydrochloride
0 ImagesCat. No.: HY-14794BCAS No.: 175131-61-0Synonyms: (1R,2S)-Milnacipran hydrochloride; F2696 hydrochlorideDextromilnacipran ((1R,2S)-Milnacipran; F2696) hydrochloride is an orally active Serotonin (HY-B1473A)/Noradrenaline (HY-13715) transporter inhibitor. Dextromilnacipran hydrochloride inhibits Serotonin and Noradrenaline reuptake. Dextromilnacipran hydrochloride can be used for the research of depression, fibromyalgia. -
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Pholedrine
0 ImagesPholedrine, the main metabolite of methamphetamine, is an indirectly acting sympathomimetic amine. Pholedrine is a cardiovascular agent exerting hypertensive and adrenergic effects. Pholedrine can produce mydriatic response and allow localization of the site of the interruption in the oculosympathetic pathway. Pholedrine can be used as a topical eye drop and a diagnostic agent for use in Horner's syndrome. -
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Pronethalol hydrochloride
0 ImagesPronethalol ((±)-Pronethalo) is a non-selective β-adrenergic antagonist. Pronethalol is a potent inhibitor of Sox2 expression. Pronethalol protects against and to reverse Digitalis-induced ventricular arrhythmias, and limits the cerebral arteriovenous malformation (AVMs). -
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MK-761 TFA
0 ImagesCat. No.: HY-123449APurity: 99.93%MK-761 TFA is an orally effective β2-adrenergic receptor antagonist. MK-761 TFA attenuates positive inotropic effects, reduces arterial pressure, enhances the contractility of papillary muscles in cat hearts, and exerts effects mediated by catecholamine release. MK-761 TFA can be used in the research of hypertension. -
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Ethoxomane
0 ImagesEthoxomane (Ethomoxane) is an α-adrenergic receptor blocker. Ethoxomane elevates the hissing threshold induced by perifornical hypothalamic stimulation in cats. Ethoxomane exhibits antihypertensive effects. Ethoxomane can be used in the research of cardiovascular and cerebrovascular diseases. -
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N-5984
0 ImagesCat. No.: HY-117378CAS No.: 220475-76-3Synonyms: KRP-204N-5984 (KRP-204) is a potent and selective agonist of β3-adrenergic receptor. N-5984 has the potential for developing as one of the clinically effective drugs for obesity and diabetes mellitus. -
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Bucindolol hydrochloride
0 ImagesCat. No.: HY-103214ACAS No.: 70369-47-0Bucindolol hydrochloride is a β-adrenergic receptor antagonist with activity in preventing new-onset atrial fibrillation. Bucindolol hydrochloride can reduce heart rate and the occurrence of bradycardia in patients with heart failure and atrial fibrillation. -
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Cimbuterol (Standard)
0 ImagesCat. No.: HY-131105RCAS No.: 54239-39-3Cimbuterol (Standard) is the analytical standard of Cimbuterol (HY-131105). This product is intended for research and analytical applications. Cimbuterol is a β-adrenergic agonist. β-adrenergic agonists act as bronchodilators and tocolytics. β-adrenergic agonists promote growth. -
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Tamsulosin-d5 hydrochloride
0 ImagesCat. No.: HY-B0661ASSynonyms: (R)-(-)-YM12617-d5; LY253351-d5Tamsulosin-d5 (hydrochloride) is the deuterium labeled Tamsulosin hydrochloride. Tamsulosin hydrochloride ((R)-(-)-YM12617) is an inhibitor of α1-adrenergic receptor. Tamsulosin hydrochloride is used for the research of prostatic hyperplasia. Tamsulosin hydrochloride attenuates abdominal aortic aneurysm growth in animal models. -
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Sotalol-d6
0 ImagesCat. No.: HY-B0437SCAS No.: 1246912-17-3Synonyms: MJ 1999-d6Sotalol-d6 is the deuterium labeled Sotalol. Sotalol is an orally active, non-selective β-adrenergic receptor blocker. Sotalol is a potent antiarrhythmic agent that can be used for the research of pediatric arrhythmias. Sotalol blocks β-receptors, and potassium KCNH2 channels. Antiepileptic Agent. -
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Sorry. There is currently no product that acts on isoform Bcl-2, Bcl-W and Bim together.Please
try each isoform separately.