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Adrenergic Receptor Isoform Specific Products
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Adrenergic Receptor Inhibitors
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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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SU-4029 dihydrochloride
0 ImagesSu-4029 is an agent that interacts with alpha receptors. It negates the blockade of norepinephrine by the reversible adrenergic blocker phentolamine but not by the irreversible blocker Dibenamine, suggesting Su-4029 acts at the same site as these blockers. Su-4029 pretreatment results in three categories of responses to pressor phenylalkylamines: irreversible blockade of amines with no or only p-hydroxylation, reversible blockade of amines with beta-carbon hydroxylation, and no blockade or augmentation of amines with m and p-hydroxylation or m or p plus beta-hydroxylation. Su-4029 may deform the alpha receptor site affected by adrenergic blocking agents. -
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Terazosin hydrochloride (Standard)
0 ImagesTerazosin (hydrochloride) (Standard) is the analytical standard of Terazosin (hydrochloride). This product is intended for research and analytical applications. Terazosin hydrochloride is a quinazoline derivative and a competitive and orally active α1-adrenoceptor antagonist. Terazosin hydrochloride works by relaxing blood vessels and the opening of the bladder. Terazosin hydrochloride has the potential for benign prostatic hyperplasia (BPH) and high blood pressure treatment. -
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Ridazolol
0 ImagesCat. No.: HY-106684CAS No.: 83395-21-5Ridazolol is a β-adrenergic receptor (βAR) antagonist. Ridazolol exhibits a high degree of selectivity for β-1 adrenergic receptor (β1AR) and possesses moderate intrinsic sympathomimetic activity (ISA). Ridazolol can competitively antagonize the relaxation effects induced by isoproterenol. Ridazolol is utilized in the research of cardiovascular diseases. -
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BMY 7378 (Standard)
0 ImagesCat. No.: HY-100554RCAS No.: 21102-95-4BMY 7378 (Standard) is the analytical standard of BMY 7378 (HY-100554). This product is intended for research and analytical applications. BMY 7378 is a selective antagonist of α1D-adrenoceptor (α1D-AR). BMY 7378 binds to membranes expressing the cloned rat α1D-AR with a >100-fold higher affinity (Ki=2 nM) than binding to either the cloned rat α1A-AR (Ki=800 nM) or the hamster α1B-AR (Ki=600 nM). BMY 7378 is a 5-HT1A receptor partial agonist. -
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Monatepil
0 ImagesCat. No.: HY-106818CAS No.: 103377-41-9Synonyms: AJ-2615 free baseMonatepil (AJ-2615 free base) is a calcium antagonist with potent α1-adrenoceptor blocking activity. Monatepil inhibits vasopressin- or methacholine-induced ischemic electrocardiographic changes in a rat model of vasospastic angina and reduces the mean arterial pressure in anesthetized rats. Monatepil also enhances low-density lipoprotein (LDL) receptor activity in human skin fibroblasts. Monatepil can be used in research related to hypertension, atherosclerosis, hyperlipidemia and vasospastic angina. -
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Tamsulosin (Standard)
0 ImagesCat. No.: HY-B0661RCAS No.: 106133-20-4Synonyms: (R)-(-)-YM12617 free base (Standard); LY253351 free base (Standard)Tamsulosin (Standard) is the analytical standard of Tamsulosin. This product is intended for research and analytical applications. Tamsulosin ((R)-(-)-YM12617 free base) is an inhibitor of α1-adrenergic receptor. Tamsulosin is used for the research of prostatic hyperplasia. Tamsulosin attenuates abdominal aortic aneurysm growth in animal models. -
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QF0301B
0 ImagesCat. No.: HY-101690CAS No.: 149247-12-1QF0301B is an α1 adrenergic receptor antagonist and a low α2 adrenoceptor, 5-HT2A, and histamine H1 receptor blocker. -
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Tertatolol
0 ImagesCat. No.: HY-U00356CAS No.: 83688-84-0Synonyms: (±)-Tertatolol; Racemic Tertatolol; dl-TertatololTertatolol is a potent antagonist of beta-adrenoceptor and 5-HT receptor, with unique renal vasodilatatory effects. -
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(4E)-SUN9221
0 ImagesCat. No.: HY-U00367CAS No.: 222318-55-0(4E)-SUN9221 is a potent antagonist of α1-adrenergic receptor and 5-HT2 receptor, with antihypertensive and anti-platelet aggregation activities. -
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Fiduxosin
0 ImagesCat. No.: HY-U00399CAS No.: 208993-54-8Fiduxosin is a potent α1-adrenoceptor antagonist, with Ki of 0.160 nM, 24.9 nM, and 0.920 nM for α1a-, α1b-, and α1d-adrenoceptors, respectively. -
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MG 1
0 ImagesCat. No.: HY-U00110CAS No.: 148274-76-4MG 1 is an α1 adrenergic receptor antagonist. -
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5-HT2 antagonist 1
0 ImagesCat. No.: HY-U00365CAS No.: 191592-09-35-HT2 antagonist 1 is a potent antagonist of 5-HT2 receptor, with weak α1 adrenoceptor blocking activity. -
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Fenmetozole Tosylate
0 ImagesCat. No.: HY-U00402CAS No.: 83474-08-2Fenmetozole Tosylate is an antagonist of the actions of ethanol, also antagonizes α2-adrenergic receptor, and acts as an antidepressant agent. -
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Bometolol Hydrochloride
0 ImagesCat. No.: HY-U00386CAS No.: 65023-16-7Bometolol Hydrochloride is a beta-adrenergic blocking agent, used for the research of cardiovascular disease. -
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Falintolol, (Z)-
0 ImagesCat. No.: HY-U00283CAS No.: 106401-52-9Falintolol, (Z)-, a new β-adrenergic antagonist, is characterized by the presence of an oxime function. -
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Phentolamine Analogue 1
0 ImagesCat. No.: HY-U00404CAS No.: 47142-51-8Phentolamine Analogue 1 is an analogue of phentolamine. Phentolamine is a nonselective alpha-adrenergic antagonist. -
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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.