Adrenergic Receptor Inhibitor
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Adrenergic Receptor Inhibitor (267)
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Dronedarone (Standard)
0 ImagesSynonyms: SR 33589 (Standard)Dronedarone (Standard) is the analytical standard of Dronedarone. This product is intended for research and analytical applications. 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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Tasipimidine sulfate (Standard)
0 ImagesCat. No.: HY-109075ARCAS No.: 1465908-73-9Tasipimidine sulfate (Standard) is the analytical standard of Tasipimidine (sulfate) (HY-109075A). This product is intended for research and analytical applications. Tasipimidine sulfate is an orally active and selective α2A-adrenoceptor agonist with a pEC50 of 7.57 for human α2A-adrenoceptors and an EC50 of 5.7 nM for rat α2-adrenoceptor. Tasipimidine sulfate can be utilized in research related to situational anxiety and fear.
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(RS)-Butyryltimolol (Standard)
0 ImagesCat. No.: HY-102032ARCAS No.: 2320274-78-8(RS)-Butyryltimolol (Standard) is the analytical standard of (RS)-Butyryltimolol. This product is intended for research and analytical applications. (RS)-Butyryltimolol is the racemate of Butyryltimolol. Butyryltimolol, an effective proagent of Timolol, improves the corneal penetration of Timolol. Butyryltimolol is a β-adrenergic blocker.
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Nomifensine maleate (Standard)
0 ImagesCat. No.: HY-B1110ARCAS No.: 32795-47-4Synonyms: (±)-Nomifensine maleate (Standard); Nomifensin maleate (Standard)Nomifensine (maleate) (Standard) is the analytical standard of Nomifensine (maleate). This product is intended for research and analytical applications. Nomifensine ((±)-Nomifensine) maleate is a potent norepinephrine (NE) and dopamine (DA) reuptake inhibitor. Nomifensine maleate inhibits uptake of NE, DA and 5-HT in rat brain synaptosomes, with IC50 values of 6.6 nM, 48 nM and 830 nM, and Ki values of 4.7 nM, 26 nM and 4000 nM, respectively. Nomifensine maleate has antidepressant and analgesic effects. Nomifensine maleate is used in neurodegenerative diseases, compound addiction, and pain research.
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Binodaline
0 ImagesCat. No.: HY-105132CAS No.: 60662-16-0Synonyms: BinedalineBinodaline is a selective norepinephrine reuptake inhibitor with a Ki of 25 nM. Binodaline can be used in the study of depressive disorder.
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Desvenlafaxine hydrochloride
0 ImagesCat. No.: HY-B0602CCAS No.: 300827-87-6Synonyms: O-Desmethylvenlafaxine hydrochlorideDesvenlafaxine (O-Desmethylvenlafaxine) hydrochloride is a selective serotonin and norepinephrine reuptake inhibitor. Desvenlafaxine (O-Desmethylvenlafaxine) hydrochloride is the major metabolite of the antidepressant venlafaxine. Desvenlafaxine (O-Desmethylvenlafaxine) hydrochloride has the potential for the research of depression and related disorders and diseases (extracted from patent WO2009049354A1).
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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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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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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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(rac)-Nebivolol-d4
0 ImagesCat. No.: HY-B0203BS1CAS No.: 1219407-55-2(rac)-Nebivolol-d4 is a labelled racemic Nebivolol. Nebivolol selectively inhibits β1- adrenergic receptor with IC50 of 0.8 nM[1][2].
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Esmolol hydrochloride (Standard)
0 ImagesEsmolol hydrochloride (Standard) is the analytical standard of Esmolol hydrochloride (HY-B1392).This product is intended for research and analytical applications. Esmolol hydrochloride is an ultra-short-acting cardioselective β1-adrenergic blocker. Esmolol hydrochloride exerts its antiarrhythmic effect by activating Neurokinin 1 ReceptorEsmolol hydrochloride attenuates post resuscitation myocardial dysfunction. Esmolol hydrochloride improves diabetic wound healing by inhibiting aldose reductase and the production of advanced glycation end products and promoting fibroblast migration. Esmolol hydrochloride can be used to study cardiac diseases such as arrhythmias and diabetic foot ulcers.
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Teoprolol
0 ImagesCat. No.: HY-U00016CAS No.: 65184-10-3Teoprolol is a β-adrenergic receptor blocker.
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Amosulalol hydrochloride
0 ImagesCat. No.: HY-106720ACAS No.: 70958-86-0Synonyms: YM 09538 hydrochlorideAmosulalol (YM 09538) hydrochloride is an orally active and dual inhibitor of α1/β1-Adrenergic Receptor. Amosulalol hydrochloride exhibits antihypertensive activity via α1-Adrenergic Receptor inhibition. Amosulalol hydrochloride decreases reflexogenic increases in heart rate and plasma renin activity (PRA) via β1-Adrenergic Receptor inhibition in spontaneously hypertensive rats (SHR).
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N-Nitrosometoprolol
0 ImagesCat. No.: HY-W726392CAS No.: 138768-62-4N-Nitrosometoprolol is an N-nitroso derivative formed by the in vitro reaction of β-adrenergic blockers with sodium nitrite. N-Nitrosometoprolol can induce micronuclei in rat liver, bone marrow and spleen.
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(Rac)-Nebivolol-d4 hydrochloride
0 ImagesCat. No.: HY-W752055CAS No.: 2701283-32-9Synonyms: (Rac)-R 065824-d4 hydrochloride(Rac)-Nebivolol-d4 hydrochloride is a labelled racemic Nebivolol. Nebivolol selectively inhibits β1-adrenergic receptor with an IC50 of 0.8 nM.
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Levobetaxolol hydrochloride (Standard)
0 ImagesSynonyms: (S)-Betaxolol hydrochloride (Standard); AL-1577A (Standard)Levobetaxolol (hydrochloride) (Standard) is the analytical standard of Levobetaxolol (hydrochloride). This product is intended for research and analytical applications.
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(S)-Alprenolol hydrochloride
0 ImagesCat. No.: HY-121692BCAS No.: 15132-12-4(S)-Alprenolol hydrochloride is a potent and nonselective β-blocker.
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YM-430
0 ImagesCat. No.: HY-19115CAS No.: 153192-22-4YM-430 is an oral active calcium entry-blocking and beta-adrenoceptor-blocking agent. YM-430 inhibits Amifampridine (HY-14946)-induced rhythmic contractions with an IC50 value of 59.2 nM and inhibits arginine vasopressin-induced ST-segment depression with an IC50 value of 36.6 mg/kg. YM-430 can be used for study of angina pectoris.
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Asenapine-d3,13C
0 ImagesCat. No.: HY-10121S4CAS No.: 1217729-73-1Synonyms: Org 5222-d3,13CAsenapine-d3,13C (Org 5222-d3,13C) is deuterium and 13C labeled Asenapine. Asenapine (Org 5222), an atypical antipsychotic, is an antagonist of serotonin receptors (pKi: 8.4-10.5), adrenoceptors (pKi: 8.9-9.5), dopamine receptors (pKi: 8.9-9.4) and histamine receptors (pKi: 8.2-9.0). Asenapine can be used in the research of schizophrenia and bipolar disorder.
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