212 Results for "

2-adrenoceptor

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

212 Results for "2-adrenoceptor" in MCE Product Catalog:

32
32 Publications Verification
Cat. No.: HY-12719
CAS No.: 113775-47-6
Purity:  99.93%
Synonyms: (+)-Medetomidine; (S)-Medetomidine
Target:  

Adrenergic Receptor

Research Areas:  

Neurological Disease Cancer

Dexmedetomidine ((+)-Medetomidine) is a potent, selective and orally active agonist of α2-adrenoceptor, with a Ki of 1.08 nM. Dexmedetomidine shows 1620-fold selectivity against α1-adrenoceptor. Dexmedetomidine exhibits anxiolysis, sedation, and modest analgesia effects [2] .
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32
32 Publications Verification
Cat. No.: HY-17034A
CAS No.: 145108-58-3
Synonyms: (+)-Medetomidine hydrochloride; (S)-Medetomidine hydrochloride
Target:  

Adrenergic Receptor

Research Areas:  

Infection Cancer

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 [2] .
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9
9 Cited Publications
Cat. No.: HY-12380A
CAS No.: 104054-27-5
Purity:  99.84%
Synonyms: MPV 1248
Target:  

Adrenergic Receptor

Research Areas:  

Neurological Disease Endocrinology

Atipamezole (MPV 1248) is a potent α2-adrenoceptor antagonist with a Ki of 1.6 nM .
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9
9 Cited Publications
Cat. No.: HY-12380
CAS No.: 104075-48-1
Purity:  99.97%
Synonyms: MPV-1248 hydrochloride
Target:  

Adrenergic Receptor

Research Areas:  

Neurological Disease Endocrinology

Atipamezole (MPV-1248) hydrochloride is a potent α2-adrenoceptor antagonist with a Ki of 1.6 nM .
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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-B0409A
CAS No.: 4205-91-8
Clonidine hydrochloride is an agonist of α2-adrenoceptor and potent antihypertensive agent.
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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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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 [2].
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5
5 Cited Publications
Cat. No.: HY-B0528A
CAS No.: 770-05-8
Synonyms: (±)-p-Octopamine hydrochloride
Octopamine ((±)-p-Octopamine) hydrochloride, a biogenic monoamine structurally related to noradrenaline, acts as a neurohormone, a neuromodulator and a neurotransmitter in invertebrates. Octopamine hydrochloride can stimulate alpha2-adrenoceptors (ARs) in Chinese hamster ovary cells transfected with human alpha2-ARs. Octopamine hydrochloride increased glycogenolysis, glycolysis, oxygen uptake, gluconeogenesis and the portal perfusion pressure [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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4
4 Cited Publications
Cat. No.: HY-12724
CAS No.: 5051-62-7
Purity:  99.85%
Research Areas:  

Cardiovascular Disease Cancer

Guanabenz is an orally active α-2-adrenoceptor agonist. Guanabenz has antihypertensive effect and antiparasitic activity. Guanabenz interferes ER stress-signalling and has protective effects in cardiac myocytes. Guanabenz also is used for the research of high blood pressure [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-12724A
CAS No.: 23113-43-1
Purity:  99.94%
Research Areas:  

Cardiovascular Disease Cancer

Guanabenz hydrochloride is an orally active α-2-adrenoceptor agonist. Guanabenz hydrochloride has antihypertensive effect and antiparasitic activity. Guanabenz hydrochloride interferes ER stress-signalling and has protective effects in cardiac myocytes. Guanabenz hydrochloride also is used for the research of high blood pressure [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-12710
CAS No.: 131-03-3
Purity:  98.27%
Synonyms: α-Yohimbine; Corynanthidine; Isoyohimbine
Rauwolscine is a selective α2-adrenoceptor antagonist that inhibits tumor growth and induces apoptosis .
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1
1 Cited Publications
Cat. No.: HY-17034
CAS No.: 86347-14-0
Target:  

Adrenergic Receptor

Research Areas:  

Neurological Disease Endocrinology

Medetomidine is an orally active α2-adrenoceptor agonist (Ki: 1.08 nM). Medetomidine has sedative and analgesic effects. Medetomidine can cause peripheral vasoconstriction through the activation of α2 adrenoceptors on blood vessels [2] .
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