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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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(R)-Propranolol-d7
0 ImagesCat. No.: HY-B0573CSCAS No.: 1346617-25-1(R)-Propranolol-d7 is the deuterium labeled (R)-Propranolol. -
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Desipramine-d3
0 ImagesCat. No.: HY-B1272AS1CAS No.: 65100-49-4Desipramine-d3 is the deuterium labeled Desipramine (HY-B1272A). Desipramine 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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(S)-Metoprolol-d7
0 ImagesCat. No.: HY-17503S2CAS No.: 1292906-91-2(S)-Metoprolol-d7 is the deuterium labeled Metoprolol. Metoprolol (Toprol) is a selective β1 receptor blocker used in treatment of several diseases of the cardiovascular system, especially hypertension[1][2]. -
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(S)-Atenolol-d7
0 ImagesCat. No.: HY-17498ASCAS No.: 1309283-20-2(S)-Atenolol-d7 is the deuterium labeled (S)-Atenolol. -
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Phenoxybenzamine-d5 hydrochloride
0 ImagesCat. No.: HY-B0431ASCAS No.: 1329838-45-0Phenoxybenzamine-d5 (hydrochloride) is the deuterium labeled Phenoxybenzamine hydrochloride. Phenoxybenzamine hydrochloride is a nonselective, irreversible, orally active α-adrenoceptor antagonist that is commonly used for the research of hypertension, specifically caused by pheochromocytoma. Phenoxybenzamine hydrochloride also shows antitumor activity[1][2][3]. -
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Atomoxetine-d3 hydrochloride
0 ImagesCat. No.: HY-110223CAS No.: 1217776-38-9Atomoxetine-d3 hydrochloride is the deuterium labeled Atomoxetine hydrochloride. Atomoxetine hydrochloride is a potent and selective noradrenalin re-uptake inhibitor (Ki values are 5, 77 and 1451 nM for inhibition of radioligand binding to human NET, SERT and DAT respectively). -
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Alfuzosin-d3 hydrochloride
0 ImagesCat. No.: HY-B0192ASCAS No.: 1216383-97-9Synonyms: SL 77499-10-d3Alfuzosin-d3 hydrochloride is the deuterium labeled Alfuzosin hydrochloride. Alfuzosin hydrochloride is an α1 adrenergic receptor antagonist used to treat benign prostatic hyperplasia (BPH). -
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(R)-Metoprolol-d7
0 Images(R)-Metoprolol-d7 is the deuterium labeled Metoprolol. Metoprolol (Toprol) is a selective β1 receptor blocker used in treatment of several diseases of the cardiovascular system, especially hypertension[1][2]. -
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Nomifensine-d3 maleate
0 ImagesCat. No.: HY-B1110SCAS No.: 1795140-41-8Synonyms: (±)-Nomifensine-d3 maleate; Nomifensin-d3 maleateNomifensine-d3 ((±)-Nomifensine-d3) maleate is the deuterium labeled Nomifensine maleate (HY-B1110A). 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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Diclofensine-d3 (hydrochloride)
0 ImagesCat. No.: HY-18610SCAS No.: 1794780-41-8Diclofensine-d3 (Ro-8-4650-d3) hydrochloride is the deuterium labeled Diclofensine hydrochloride. Diclofensine hydrochloride is an orally active neuronal monoamine uptake inhibitor. Diclofensine hydrochloride blocks the uptake of dopamine, noradrenaline, and serotonin by rat brain synaptosomes with IC50 values of 0.74, 2.3 and 3.7 nM, respectively. Diclofensine hydrochloride potentiates norepinephrine-induced hypertension and attenuates Tyramine (HY-W007606)-induced hypertension. Diclofensine hydrochloride produces psychostimulant and mood-elevating effects without causing sudden disappearance or withdrawal reactions. Diclofensine hydrochloride can be used in the research of moderate to severe depression. -
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Prazobind-d8
0 ImagesCat. No.: HY-118335SCAS No.: 1189701-23-2Synonyms: SZL 49-d8Prazobind-d8 (SZL 49-d8) is the deuterium labeled Prazobind (HY-118335). Prazobind, a prazosin analog, is an irreversible α1-adrenoceptor antagonist. Prazobind competes for alpha 1-adrenoceptor binding sites with a similar potency (IC50 of 1 nM) in tissues enriched in both the alpha 1A (hippocampus) and alpha 1B (liver) subtypes. Prazobind partially inhibits the contractions of circular muscles, longitudinal muscles and smooth muscles of the spleen. Prazobind can be used for the study of blood pressure. -
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Clonidine-d4 hydrochloride
0 ImagesCat. No.: HY-12721SCAS No.: 67151-02-4Clonidine-d4 (hydrochloride) is the deuterium labeled Clonidine. Clonidine hydrochloride is an alpha 2-adrenergic agonist. -
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Medetomidine-d3 hydrochloride
0 ImagesCat. No.: HY-17034BSCAS No.: 1246820-20-1Synonyms: MPV785-d3Medetomidine-d3 (hydrochloride) is the deuterium labeled Medetomidine hydrochloride. Medetomidine hydrochloride is an agonist of adrenergic alpha-2 receptor. -
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(Rac)-Tamsulosin-d3 hydrochloride
0 ImagesCat. No.: HY-B0661CSCAS No.: 1189923-88-3(Rac)-Tamsulosin-d3 hydrochloride is the deuterated-labeled Tamsolusin hydrochloride (HY-B0661C). Tamsolusin hydrochloride (YM12617 hydrochloride; LY253351 hydrochloride) is an isomer of Tamsulosin (HY-B0661). Tamsolusin hydrochloride is a sulfonamide phenethylamine derivative and a competitive antagonist of selective post-synaptic α1-adrenoceptors. Tamsolusin hydrochloride inhibits CYP3A4 activity in a non-competitive, enantiomer-specific manner, with an IC50 and Ki of 6.75 μM. Tamsolusin hydrochloride produces dose-dependent hypotension, preferentially antagonizing α1-adrenoceptor-mediated pressor responses, and inhibits α2-adrenoceptor-mediated pressor responses at high doses. Tamsolusin hydrochloride can be used in research related to various diseases such as metabolism. -
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Terbutaline-d9
0 ImagesCat. No.: HY-B0802ASCAS No.: 1189658-09-0Terbutaline-d9 is the deuterium labeled Terbutaline. -
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Carteolol-d9 hydrochloride
0 ImagesCat. No.: HY-17495ASCAS No.: 1346602-13-8Synonyms: OPC-1085-d9 hydrochlorideCarteolol-d9 (hydrochloride) is the deuterium labeled Carteolol hydrochloride. Carteolol hydrochloride (OPC-1085 hydrochloride) is a non-selective beta blocker used to treat glaucoma. -
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Indacaterol-d3
0 ImagesCat. No.: HY-14299SCAS No.: 2699828-16-3Indacaterol-d3 is deuterium labeled Indacaterol. -
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Azepexole
0 ImagesCat. No.: HY-103212BCAS No.: 36067-73-9Synonyms: B-HT 933Azepexole (B-HT 933) is a selective α2 adrenergic inducer with over 300-fold selectivity for α2 adrenergic receptors over α1 adrenergic receptors. Azepexole can be used to study the biological functions of α2 adrenergic receptors and inhibition of related diseases. Azepexole may also play a role in regulating mood and improving cognitive function. -
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Naftopidil-d5
0 ImagesCat. No.: HY-B0391S1CAS No.: 2747918-58-5Synonyms: KT-611-d5; BM-15275-d5Naftopidil-d5 is deuterium labeled Naftopidil. Naftopidil (KT-611) is is a selective alpha1-adrenoceptor antagonist, with Kis of 3.7 nM, 20 nM and 1.2 nM for the cloned human α1a-, α1b- and α1d-adrenoceptor subtypes, respectively. Naftopidil has antiproliferative effects. Naftopidil can be used for the research of prostate hyperplasia. -
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Solabegron hydrochloride
0 ImagesCat. No.: HY-19436ACAS No.: 451470-34-1Synonyms: GW 427353BSolabegron hydrochloride is a selective β3-adrenergic receptor agonist, stimulating cAMP accumulation in Chinese hamster ovary cells expressing the human β3-AR, with an EC50 value of 22 nM. Solabegron hydrochloride (GW 427353) is being developed for the treatment of overactive bladder and irritable bowel syndrome. -
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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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