95 Results for "

β2-adrenoceptor

" in MedChemExpress (MCE) Product Catalog:
Products (95)

95 Results for "β2-adrenoceptor" in MCE Product Catalog:

8
8 Publications Verification
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 Publications Verification
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-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 [2].
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7
7 Cited Publications
Cat. No.: HY-B0010B
CAS No.: 73573-87-2
Synonyms: (±)Formoterol
Target:  

Adrenergic Receptor

Research Areas:  

Inflammation/Immunology

Formoterol ((±)Formoterol) is a selective β2-adrenoceptor agonist. Formoterol is at least as β2-adrenoceptor selective as Salbutamol (HY-B1037) and Terbutaline (HY-B0802A). Formoterol abolishs the contraction induced by Acetylcholine in bronchioles. Formoterol can be used for the research of chronic obstructive pulmonary disease and bronchial asthma [2].
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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 [2] .
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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 [2] .
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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 [2] .
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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 [2] .
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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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2
2 Cited Publications
Cat. No.: HY-14301A
CAS No.: 869477-96-3
Purity:  99.70%
Synonyms: BI1744 hydrochloride
Olodaterol (BI1744) hydrochloride 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 [2] .
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2
2 Cited Publications
Cat. No.: HY-W011733
CAS No.: 56776-01-3
Synonyms: C-78
Tulobuterol 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 [2].
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1
1 Cited Publications
Cat. No.: HY-14304A
CAS No.: 38241-28-0
Purity:  99.34%
Synonyms: MJ 9184 hydrochloride
Target:  

Adrenergic Receptor

Research Areas:  

Cardiovascular Disease

Zinterol hydrochloride (MJ 9184 hydrochloride) is a potent and selective β2-adrenoceptor agonist . Zinterol hydrochloride increases ICa in a concentration-dependent manner with an EC50 of 2.2 nM [2]. Zinterol hydrochloride induces ventricular arrhythmias in conscious heart failure rabbits .
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1
1 Cited Publications
Cat. No.: HY-107327
CAS No.: 57775-29-8
Purity:  99.71%
Synonyms: (±)-Carazolol; DL-Carazolol; Suacron
Target:  

Adrenergic Receptor

Research Areas:  

Cardiovascular Disease

Carazolol is a β12 adrenoceptor antagonist of high potency used in the research of hypertension. Carazolol is also a potent, selective β3-adrenoceptor agonist .
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1
1 Cited Publications
Cat. No.: HY-B1035
CAS No.: 27912-14-7
Synonyms: l-Bunolol hydrochloride
Levobunolol (l-Bunolol) hydrochloride is a non-selective β-adrenergic antagonist and vasodilator. By blocking calcium ion influx and reducing the sensitivity of vascular smooth muscle to calcium, Levobunolol hydrochloride effectively dilates the ciliary arteries and increases ocular blood flow, so it is widely used in research on glaucoma and ocular hypertension. Levobunolol hydrochloride inhibits the β-receptor signaling pathway and the expression of related proliferation markers (such as CK3, CK14, CK19, Ki67) in corneal cells. In rabbit models, Levobunolol hydrochloride not only does not inhibit corneal epithelial regeneration, but also accelerates the healing of mechanical injury without adverse effects. Levobunolol hydrochloride also inhibits histamine-induced vasoconstriction and intracellular calcium elevation, exhibiting unique vascular regulatory activity. Levobunolol hydrochloride protects ocular blood flow and promotes corneal repair [2] .
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Cat. No.: HY-B0976
CAS No.: 13392-18-2
Synonyms: Th-1165; Phenoterol
Fenoterol (Th-1165), a sympathomimetic agent, is a selective and orally active β2-adrenoceptor agonist. Fenoterol is an effective bronchodilator and can be used for bronchospasm associated with asthma, bronchitis and other obstructive airway diseases research [2].
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Cat. No.: HY-B0976A
CAS No.: 1944-12-3
Synonyms: Th-1165a; Phenoterol hydrobromide
Fenoterol hydrobromide (Th-1165a), a sympathomimetic agent, is a selective and orally active β2-adrenoceptor agonist. Fenoterol hydrobromide is an effective bronchodilator and can be used for bronchospasm associated with asthma, bronchitis and other obstructive airway diseases research [2].
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Cat. No.: HY-W744625
Synonyms: BI1744-d3 hydrochloride
Olodaterol-d3 hydrochloride (BI1744-d3 hydrochloride) is the deuterium labeled Olodaterol hydrochloride (HY-14301A). Olodaterol (BI1744) hydrochloride is a selective, long acting β2-adrenoceptor (β2-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 [2] .
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Cat. No.: HY-12463
CAS No.: 137888-11-0
Purity:  98.73%
Target:  

Adrenergic Receptor

Research Areas:  

Inflammation/Immunology

Carmoterol hydrochloride is a highly potent, selective and long-acting β2-adrenoceptor agonist with the pEC50 of 10.19. Carmoterol has 53 times higher affinity for the β2-adrenoceptors than for the β1-adrenoceptors. Carmoterol hydrochloride can be used for the research of asthma and chronic obstructive pulmonary disease (COPD) [2].
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Cat. No.: HY-12980
CAS No.: 743461-65-6
Purity:  98.30%
Synonyms: GSK961081; TD-5959
Batefenterol (GSK961081;TD-5959) is a novel muscarinic receptor antagonist and β2-adrenoceptor agonist; displays high affinity for hM2, hM3 muscarinic and hβ2-adrenoceptor with Ki values of 1.4, 1.3 and 3.7 nM, respectively.
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Cat. No.: HY-101355B
CAS No.: 105737-62-0
Purity:  ≥99.0%
Synonyms: CGP 20712 mesylate
Target:  

Adrenergic Receptor

Research Areas:  

Cardiovascular Disease

CGP 20712 A (CGP 20712 mesylate) is a highly selective β1-adrenoceptor antagonist with an IC50 of 0.7 nM. CGP 20712 A exhibits ~10,000-fold selectivity over β2-adrenoceptors .
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