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Adrenergic Receptor Isoform Specific Products
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Adrenergic Receptor Related Products (1647)
Related Products (1647)
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Antibodies (4)
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Adrenergic Receptor Isoform Comparison
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Tolamolol
0 ImagesCat. No.: HY-159802CAS No.: 38103-61-6Tolamolol is a selective beta-adrenergic antagonist with significant activity in reducing exercise-induced ST-segment depression. Tolamolol is clinically equivalent to propranolol in suppressing angina and exhibits greater cardiac selectivity. Tolamolol is effective in reducing the frequency of angina attacks and the amount of glyceryl trinitrate used. Tolamolol is effective in lowering blood pressure and has a positive effect on increasing the amount of exercise that can be performed before angina attacks. The use of Tolamolol also helps improve the suppression of arrhythmias. -
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R 47 243
0 ImagesCat. No.: HY-114514CAS No.: 104383-18-8R 47 243 is a potent racemic alpha 2 antagonist. R 47 243 has the potential for Parkinson's disease research. -
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Setiptiline-d3
0 ImagesCat. No.: HY-32329SCAS No.: 1795024-97-3Setiptiline-d3 is the deuterium labeled Setiptiline. Setiptiline (Org-8282) is a serotonin receptor antagonist. Setiptiline is a tetracyclic antidepressant (TeCA) which acts as a noradrenergic and specific serotonergic antidepressant (NaSSA). Setiptiline acts as a norepinephrine reuptake inhibitor, α2-adrenergic receptor antagonist, and serotonin receptor antagonist, likely at the 5-HT2A, 5-HT2C, and/or 5-HT3 subtypes, as well as an H1 receptor inverse agonist/antihistamine. -
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Esmolol
0 ImagesCat. No.: HY-B1392ACAS No.: 81147-92-4Esmolol is an ultra-short-acting cardioselective β1-adrenergic blocker. Esmolol exerts its antiarrhythmic effect by activating Neurokinin 1 Receptor. Esmolol attenuates post resuscitation myocardial dysfunction. Esmolol improves diabetic wound healing by inhibiting aldose reductase and the production of advanced glycation end products and promoting fibroblast migration. Esmolol can be used to study cardiac diseases such as arrhythmias and diabetic foot ulcers. -
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Medroxalol hydrochloride
0 ImagesCat. No.: HY-101656ACAS No.: 70161-10-3Synonyms: RMI81968 hydrochlorideMedroxalol hydrochloride is an orally active adrenergic receptor antagonist, blocks α- and β-adrenergic receptors. Medroxalol hydrochloride shows antihypertensive and vasodilating effects. -
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Mirabegron-d5
0 ImagesCat. No.: HY-14773S3CAS No.: 1258889-45-0Synonyms: YM178-d5Mirabegron-d5 (YM178-d5) is deuterium labeled Mirabegron. Mirabegron is a selective β3-adrenoceptor agonist with EC50 of 22.4 nM. -
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5-Hydroxy propranolol
0 ImagesCat. No.: HY-129254CAS No.: 81907-82-65-Hydroxy propranolol is a metabolite of Propranolol that can be used to study β-adrenergic receptor blockade. -
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Dopexamine
0 ImagesCat. No.: HY-106562CAS No.: 86197-47-9Synonyms: FPL 60278Dopexamine is a β2 adrenergic receptor agonist. -
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Zenidolol hydrobromide (Standard)
0 ImagesCat. No.: HY-13951RCAS No.: 72795-01-8Synonyms: ICI-118551 hydrobromide (Standard)Zenidolol hydrochloride (Standard) is the analytical standard of Zenidolol hydrochloride (HY-13951). This product is intended for research and analytical applications. Zenidolol (ICI-118551) hydrochloride is a highly selective β2 adrenergic receptor antagonist, with Kis of 0.7, 49.5 and 611 nM for β2, β1 and β3 receptors, respectively. -
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Zenidolol (Standard)
0 ImagesCat. No.: HY-100543RCAS No.: 72795-26-7Synonyms: ICI-118551 (Standard)Zenidolol (ICI-118551) (Standard) is the analytical standard of Zenidolol (HY-100543). This product is intended for research and analytical applications. Zenidolol is a selective β2-adrenergic receptor antagonist with Ki values of Zenidolol for β2, β1 and β3 adrenergic receptors of 0.7, 49.5 and 611 nM, respectively. Zenidolol exerts antitumor effects via inducing apoptosis, inhibiting tumor sphere formation, and downregulating the HIF pathway by blocking β2-AR on tumor cells. Zenidolol exhibits a unique pulmonary vessel-specific vasodilatory effect in mouse models. Zenidolol can be used as an intraocular pressure-lowering agent in ophthalmic disease research. -
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AR ligand-50
0 ImagesAR ligand-50 (Compound 4) is an adrenergic receptor ligand (pKi: 7.14 for human α2-adrenergic receptor on CHO cells). AR Ligand-50 can be used in the research of neurological disorders. -
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Abanoquil (Standard)
0 ImagesCat. No.: HY-106612RCAS No.: 90402-40-7Synonyms: U-K52046 (Standard); Albanoquil (Standard)Abanoquil (Standard) is the analytical standard of Abanoquil (HY-106612). This product is intended for research and analytical applications. Abanoquil (U-K52046), an potent and selective α-1 adrenoceptor antagonist, is an anti-arrhythmic agent. Abanoquil can be used for erectile dysfunction research. -
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KUL-7211
0 ImagesCat. No.: HY-19673CAS No.: 220129-58-8KUL 7211 is a selective β-adrenoceptor agonist. -
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Vilanterol-d12
0 ImagesCat. No.: HY-14300S2Synonyms: GW642444-d12Vilanterol-d12 (GW642444-d12) is deuterium labeled Vilanterol. Vilanterol (GW642444) is a long-acting β2-adrenoceptor (β2-AR) agonist with 24 h activity. The pEC50s for β2-AR,β1-AR and β3-AR is 10.37±0.05, 6.98±0.03 and 7.36±0.03, respectively. -
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Silodosin-d4
0 ImagesCat. No.: HY-10122SCAS No.: 1426173-86-5Silodosin-d4 is the deuterium labeled Silodosin. Silodosin (KAD 3213) is a potent, selective and orally active α1A-adrenergic receptor (α1A-AR) blocker. Silodosin exhibits high affinity for α1A-AR (Ki=0.036 nM), over 162-fold and 50-fold than for α1B-AR and α1D-AR with Ki values of 21 nM and 2.0 nM, respectively. Silodosin is an effective and well-tolerated agent, it can be used for the investigation of LUTS/BPH. -
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Carbazochrome (sodium sulfonate trihydrate)
0 ImagesCat. No.: HY-W1059167CAS No.: 2666934-58-1Synonyms: AC-17 trihydrateCarbazochrome sodium sulfonate trihydrate (AC-17 trihydrate) is a capillary stabilizer with anti-hemorrhagic properties and can be used in hemostasis-related research. -
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Lofepramine (Standard)
0 ImagesSynonyms: Lopramine (Standard)Lofepramine (Standard) is the analytical standard of Lofepramine. This product is intended for research and analytical applications. Lofepramine (Lopramine) is a modified tricyclic and orally active antidepressant. Lofepramine inhibits the uptake of Noradrenaline (NA) (HY-13715) and 5-hydroxytryptamine (5-HT) with IC50s of 2.7 μM and 11 μM, respectively. Lofepramine exerts its antidepressant activity by promoting noradrenergic neurotransmission. Lofepramine also enhances serotonergic neurotransmission by inhibiting neuronal uptake of 5-HT and tryptophan pyrrolase. Lofepramine exhibits significant anxiolytic properties. . -
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Ractopamine-d3 (hydrochloride)
0 ImagesSynonyms: LY031537-d3Ractopamine-d3 (LY031537-d3) hydrochloride is the deuterium labeled Ractopamine hydrochloride (HY-B1421). Ractopamine hydrochloride (LY031537) is a potent and orally active β-adrenergic receptor (βAR) agonist with Kd value of ~25 nM for pig β1AR and β2AR. Ractopamine hydrochloride also is a mTAAR1 agonist with an EC50 of 16 μM. Ractopamine hydrochloride promotes muscle mass development, limits fat deposition, reduces feed consumption, increases total cellular protein synthesis, and improves growth rate and feed efficiency in finishing swine. Ractopamine hydrochloride can be used for researching to increase lean tissue growth and improve production efficiency in pigs. -
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Dronedarone-d6
0 ImagesCat. No.: HY-A0016S3CAS No.: 1132693-87-8Synonyms: SR 33589-d6Dronedarone-d6 (SR 33589-d6) is deuterium labeled Dronedarone. Dronedarone (SR 33589), a derivative of amiodarone (HY-14187), is a class III antiarrhythmic agent for the study of atrial fibrillation (AF) and atrial flutter. Dronedarone is a potent blocker of multiple ion currents, including potassium current, sodium current, and L-type calcium current, and exhibits antiadrenergic effects by noncompetitive binding to β-adrenergic receptors. Dronedarone is a substrate for and a moderate inhibitor of CYP3A4. -
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L-748328
0 ImagesCat. No.: HY-118944CAS No.: 244192-93-6L-748328 is a potent and selective human β3-adrenergic receptor antagonist. L-748328 has a Ki of 3.7 nM against human cloned β3-AR expressed in Chinese hamster ovary (CHO) cells. In addition, L-748328 inhibits the lipolytic response induced by the β3-AR agonist L-742791 in isolated non-human primate adipocytes. -
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Sorry. There is currently no product that acts on isoform Bcl-2, Bcl-W and Bim together.Please
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