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Adrenergic Receptor
Beta Receptor
Adrenergic Receptor Isoform Specific Products
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Adrenergic Receptor Ligands
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Adrenergic Receptor Related Products (1630)
Related Products (1630)
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Antibodies (4)
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Adrenergic Receptor Isoform Comparison
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Tedatioxetine hydrobromide
0 ImagesSynonyms: Lu AA24530 hydrobromideTedatioxetine (Lu AA24530) hydrobromide acts as a serotonin and norepinephrine (NE)-preferring triple reuptake inhibitor (TRI) and 5-HT2A, 5-HT2C, 5-HT3 and α1A-adrenergic receptor antagonist. , -
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Indanidine
0 ImagesIndanidine is a selective alpha-adrenergic agonist. Indanidine shows a partial agonist in rat aorta. -
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Lidanserin
0 ImagesCat. No.: HY-101815CAS No.: 73725-85-6Synonyms: ZK-33839Lidanserin (ZK-33839) acts as a 5-HT2A and α1-adrenergic receptor antagonist. -
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Xamoterol
0 ImagesCat. No.: HY-101327CAS No.: 81801-12-9Synonyms: Corwin; ICI 118587Xamoterol (Corwin; ICI 118587) is an orally active and selective β1-adrenoceptor partial agonist. Xamoterol acts as agonist at low sympathetic tone, antagonist at high sympathetic tone, with context-dependent cardiovascular effects including modulated heart rate, blood pressure, and cardiac output. Xamoterol can be used for the research of heart failure, postural hypotension, and ischemic heart disease. -
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(RS)-Butyryltimolol
0 Images(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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α2A-AR agonist 1
0 Imagesα2A-AR agonist 1 (Compound B9) is a selective agonist for α2-adrenergic receptor (α2A-AR) with EC50 of 0.23 nM. α2A-AR agonist 1 exhibits a hypnotic effect, with ED50 of 0.138 mg/kg in the loss of righting reflex (LORR) experiment. α2A-AR agonist 1 exhibits metabolic stability in mouse liver microsomes. -
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Isoxsuprine-d6 hydrochloride
0 ImagesIsoxsuprine-d6 (hydrochloride) is the deuterium labeled Isoxsuprine hydrochloride. Isoxsuprine hydrochloride is a beta-adrenergic receptor agonist with Kis of 13.65 μΜ and 3.48 μΜ for myometrial and placcntal beta-adrenergic receptor, respectively. Isoxsuprine hydrochloride is also a NMDA receptor antagonist. -
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L-771688
0 ImagesL-771688 is a highly selective α1A-Adrenoceptor antagonist with a Ki of 0.43±0.02 nM. -
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ARC 239
0 ImagesARC 239 is an α2B/C-adrenergic receptor antagonist with pKi of 7.06 and 6.95 for rat kidney α2B and human α2C, respectively. ARC 239 also inhibits 5-HT1A receptor with a Ki of 63.1 nM. -
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Midaglizole hydrochloride
0 ImagesSynonyms: (±)-DG5128; DG5128Midaglizole hydrochloride (DG5128) is a preferential α2-adrenoceptor antagonist. Midaglizole hydrochloride (DG5128) exhibits 7.4 times higher affinity (pKi=6.28) toward α2-adrenoceptor than α1-adrenoceptor. -
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Tulobuterol hydrochloride
0 ImagesSynonyms: C-78Tulobuterol hydrochloride (C-78) is a long-acting β2-adrenoceptor agonist, which reduces the frequency of exacerbations of chronic obstructive pulmonary disease and bronchial asthma. Tulobuterol hydrochloride is also a sympathomimetic agent used as a transdermal patch, increases normal diaphragm muscle strength. Tulobuterol hydrochloride inhibit rhinovirus replication and modulate airway inflammation. -
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Nafetolol
0 ImagesSynonyms: K 5407 free baseNafetolol (K 5407 free base) is a β1-selective blocker with high hepatic clearance in humans and dogs, and undergoes extrahepatic, high-level metabolism. -
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Romifidine
0 ImagesCat. No.: HY-119456CAS No.: 65896-16-4Romifidine is an α2 adrenergic receptor agonist. Romifidine shows sedation effects in vivo. -
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Zinterol
0 ImagesCat. No.: HY-14304CAS No.: 37000-20-7Synonyms: MJ 9184Zinterol (MJ 9184) is a potent and selective β2-adrenoceptor agonist. Zinterol increases ICa in a concentration-dependent manner with an EC50 of 2.2 nM. -
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ST1936
0 ImagesST1936 is a selective, nanomolar affinity 5-HT6 receptor agonist with Ki values of 13 nM, 168 nM and 245 nM for human 5-HT6, 5-HT7 and 5-HT2B receptors, respectively. ST1936 also shows moderate affinity (Ki of 300 nM) for human and rat α2 adrenergic receptor. -
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Cimbuterol
0 ImagesCimbuterol is a β-adrenergic agonist. β-adrenergic agonists act as bronchodilators and tocolytics. β-adrenergic agonists promote growth. -
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Dexmedetomidine-13C,d3 hydrochloride
0 ImagesCat. No.: HY-17034ASSynonyms: (+)-Medetomidine-13C,d3 hydrochloride; (S)-Medetomidine-13C,d3 hydrochlorideDexmedetomidine-13C,d3 (hydrochloride) is the 13C- and deuterium labeled Dexmedetomidine (hydrochloride). Dexmedetomidine hydrochloride ((+)-Medetomidine hydrochloride) is a potent, selective and orally active agonist of α2-adrenoceptor, with a Ki of 1.08 nM. Dexmedetomidine hydrochloride shows 1620-fold selectivity against α1-adrenoceptor. Dexmedetomidine hydrochloride exhibits anxiolysis, sedation, and modest analgesia effects. -
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Oxyfedrine
0 ImagesCat. No.: HY-112070CAS No.: 15687-41-9Oxyfedrine, a vasodilator, is an orally active β-adrenoreceptor agonist. Oxyfedrine decreases the tonicity of coronary vessels. Oxyfedrine can be used in the research of cardiovascular disease. -
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AGN 192836
0 ImagesAGN 192836 is a potent and selective α2 adrenergic agonist with EC50s of 8.7, 41 and 6.6 nM for α2A, α2B and α2C receptor, respectively. -
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Alfuzosin-d3
0 ImagesSynonyms: SL 77499-d3Alfuzosin-d3 is deuterium labeled Alfuzosin. -
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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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