212 Results for "

beta adrenoceptor

" in MedChemExpress (MCE) Product Catalog:
Products (212)

212 Results for "beta adrenoceptor" in MCE Product Catalog:

28
28 Publications Verification
Cat. No.: HY-116771
CAS No.: 183720-02-7
Purity:  99.37%
Target:  

Adrenergic Receptor

Research Areas:  

Metabolic Disease

CL316243 free acid is a highly potent selective β3-adrenoceptor agonist with a EC50 of 3 nM, but is an extremely poor to β1/2- receptors. CL316243 free acid is a effective stimulant of adipocyte lipolysis and increases brown adipose tissue thermogenesis and metabolic rate. CL316243 free acid has the potential for the treatment obesity, diabetes and urge urinary incontinence .
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28
28 Publications Verification
Cat. No.: HY-116771A
CAS No.: 138908-40-4
Purity:  99.98%
Target:  

Adrenergic Receptor

Research Areas:  

Metabolic Disease

CL316243 is a highly potent selective β3-adrenoceptor agonist with a EC50 of 3 nM, but is an extremely poor to β1/2- receptors .CL316243 is a effective stimulant of adipocyte lipolysis and increases brown adipose tissue thermogenesis and metabolic rate . CL316243 has the potential for the treatment obesity, diabetes and urge urinary incontinence .
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21
21 Cited Publications
Cat. No.: HY-17498
CAS No.: 29122-68-7
Synonyms: (RS)-Atenolol
Atenolol ((RS)-Atenolol) is a cardioselective β1-adrenergic receptor blocker, with a Ki of 697 nM at β1-adrenoceptor in guine pig left ventricle membrane. Atenolol can be used for the research of hypertension and angina pectoris .
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17
17 Cited Publications
Cat. No.: HY-15477
CAS No.: 132836-42-1
Purity:  99.92%
YS-49 is a PI3K/Akt (a downstream target of RhoA) activator, to reduce RhoA/PTEN activation in the 3-methylcholanthrene-treated cells. YS-49 inhibits angiotensin II (Ang II)-stimulated proliferation of VSMCs via induction of heme oxygenase (HO)-1. YS-49 is also an isoquinoline compound alkaloid, has a strong positive inotropic action through activation of cardiac β-adrenoceptors .
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17
17 Cited Publications
Cat. No.: HY-15477A
CAS No.: 3028631-24-2
Purity:  99.71%
YS-49 (monohydrate) is a PI3K/Akt (a downstream target of RhoA) activator, to reduce RhoA/PTEN activation in the 3-methylcholanthrene-treated cells. YS-49 inhibits angiotensin II (Ang II)-stimulated proliferation of VSMCs via induction of heme oxygenase (HO)-1. YS-49 is also an isoquinoline compound alkaloid, has a strong positive inotropic action through activation of cardiac β-adrenoceptors .
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16
16 Cited Publications
Cat. No.: HY-17503
CAS No.: 51384-51-1
Metoprolol is an orally active, selective β1-adrenoceptor antagonist. Metoprolol shows anti-inflammation, antitumor and anti-angiogenic properties .
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16
16 Cited Publications
Cat. No.: HY-17503B
CAS No.: 56392-17-7
Metoprolol tartrate is an orally active, selective β1-adrenoceptor antagonist. Metoprolol tartrate shows anti-inflammation, antitumor and anti-angiogenic properties .
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16
16 Cited Publications
Cat. No.: HY-17503A
CAS No.: 98418-47-4
Metoprolol succinate is an orally active, selective β1-adrenoceptor antagonist. Metoprolol succinate shows anti-inflammation, antitumor and anti-angiogenic properties .
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9
9 Cited Publications
Cat. No.: HY-B1517
CAS No.: 13655-52-2
Synonyms: (RS)-Alprenolol; dl-Alprenolol
Target:  

5-HT Receptor

Research Areas:  

Cardiovascular Disease Cancer

Alprenolol ((RS)-Alprenolol; dl-Alprenolol) is an orally active non-selective β-adrenoceptor antagonist and an antagonist of 5-HT1A and 5-HT1B receptors. Alprenolol is used as an anti-hypertensive, anti-anginal and anti-arrhythmic agent .
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9
9 Cited Publications
Cat. No.: HY-B1517A
CAS No.: 13707-88-5
Synonyms: (RS)-Alprenolol hydrochloride; dl-Alprenolol hydrochloride
Target:  

5-HT Receptor

Research Areas:  

Cardiovascular Disease Cancer

Alprenolol ((RS)-Alprenolol; dl-Alprenolol) hydrochloride is an orally active non-selective β-adrenoceptor antagonist and an antagonist of 5-HT1A and 5-HT1B receptors. Alprenolol hydrochloride is used as an anti-hypertensive, anti-anginal and anti-arrhythmic agent .
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8
8 Cited Publications
Cat. No.: HY-14302
CAS No.: 89365-50-4
Purity:  99.70%
Synonyms: GR33343X
Salmeterol (GR33343X) is a potent and selective human β2 adrenoceptor agonist. Salmeterol shows potent stimulation of cAMP accumulation in CHO cells expressing human β2, β1 and β3 adrenoceptors with pEC50s of 9.6, 6.1, and 5.9, respectively .
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8
8 Cited Publications
Cat. No.: HY-17453
CAS No.: 94749-08-3
Synonyms: GR 33343X xinafoate
Salmeterol (GR 33343X) xinafoate is a potent and selective human β2 adrenoceptor agonist. Salmeterol shows potent stimulation of cAMP accumulation in CHO cells expressing human β2, β1 and β3 adrenoceptors with pEC50s of 9.6, 6.1, and 5.9, respectively .
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7
7 Cited Publications
Cat. No.: HY-108901
CAS No.: 183814-30-4
Purity:  99.91%
Formoterol hemifumarate hydrate is a selective, long-acting beta 2-adrenoceptor agonist. Formoterol is a bronchodilator used for the research of the asthma and chronic obstructive pulmonary disease (COPD). Formoterol hemifumarate hydrate induces mitochondrial biogenesis and promotes cognitive recovery after traumatic brain injury .
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6
6 Cited Publications
Cat. No.: HY-B0010
CAS No.: 43229-80-7
Synonyms: (±)Formoterol fumarate
Target:  

Adrenergic Receptor

Research Areas:  

Inflammation/Immunology

Formoterol fumarate ((±)Formoterol fumarate) is a selective β2-adrenoceptor agonist. Formoterol fumarate is at least as β2-adrenoceptor selective as Salbutamol (HY-B1037) and Terbutaline (HY-B0802A). Formoterol fumarate abolishs the contraction induced by Acetylcholine in bronchioles. Formoterol fumarate can be used for the research of chronic obstructive pulmonary disease and bronchial asthma .
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6
6 Cited Publications
Cat. No.: HY-17380
CAS No.: 26921-17-5
Synonyms: (S)-L-714,465 maleate; MK 950
(S)-Timolol Maleate (L-714,465 Maleate) is a non-cardioselective hydrophilic β-adrenoceptor blocker. (S)-Timolol Maleate is widely used as standard medication for intraocular pressure (glaucoma) by preventing the production of aqueous humor. (S)-Timolol Maleate can be used for hypertension, angina pectoris and myocardial infarction .
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5
5 Cited Publications
Cat. No.: HY-14773
CAS No.: 223673-61-8
Purity:  99.90%
Synonyms: YM178
Mirabegron is a selective β3-adrenoceptor agonist with EC50 of 22.4 nM.
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5
5 Cited Publications
Cat. No.: HY-15746
CAS No.: 49745-95-1
Purity:  99.60%
Dobutamine hydrochloride is a synthetic catecholamine that acts on α1-AR, β1-AR, β2-AR (α-1, β-1 andβ-2 adrenoceptors). Dobutamine hydrochloride is a selective β1-AR agonist, relatively weak activity at α1-AR and β2-AR. Dobutamine hydrochloride can increase cardiac output and correct hypoperfusion .
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5
5 Cited Publications
Cat. No.: HY-15746A
CAS No.: 34368-04-2
Dobutamine is a synthetic catecholamine that acts on α1-AR, β1-AR, β2-AR (α-1, β-1 andβ-2 adrenoceptors). Dobutamine is a selective β1-AR agonist, relatively weak activity at α1-AR and β2-AR. Dobutamine can increase cardiac output and correct hypoperfusion .
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2
2 Cited Publications
Cat. No.: HY-14301
CAS No.: 868049-49-4
Purity:  98.47%
Synonyms: BI1744
Olodaterol (BI1744) is a selective, long acting β2-adrenoceptor 2-AR) agonist (EC50=0.1 nM and pKi= 9.14 for human β2-adrenoceptor, respectively). Olodaterol can be used for chronic obstructive pulmonary disease (COPD) and pulmonary fibrosis .
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2
2 Cited Publications
Cat. No.: HY-B1810
CAS No.: 41570-61-0
Synonyms: C-78 free base
Tulobuterol (C-78 free base) is a long-acting β2-adrenoceptor agonist, which reduces the frequency of exacerbations of chronic obstructive pulmonary disease and bronchial asthma. Tulobuterol is also a sympathomimetic agent used as a transdermal patch, and increases normal diaphragm muscle strength .
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