130 Results for "

alpha 2-adrenoceptor

" in MedChemExpress (MCE) Product Catalog:
Products (130)

130 Results for "alpha 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 .
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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 .
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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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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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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 .
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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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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 .
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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 .
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1
1 Cited Publications
Cat. No.: HY-B0352
CAS No.: 85650-52-8
Synonyms: Org3770; 6-Azamianserin
Mirtazapine (Org3770) is a potent and orally active noradrenergic and specific serotonergic antidepressant (NaSSA) agent. Mirtazapine is also a 5-HT2, 5-HT3, histamine H1 receptor and α2-adrenoceptor antagonist with pKi values of 8.05, 8.1, 9.3 and 6.95, respectively .
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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 .
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1
1 Cited Publications
Cat. No.: HY-17034B
CAS No.: 86347-15-1
Synonyms: MPV785
Target:  

Adrenergic Receptor

Research Areas:  

Neurological Disease Endocrinology

Medetomidine hydrochloride is an orally active α2-adrenoceptor agonist (Ki: 1.08 nM). Medetomidine hydrochloride has sedative and analgesic effects. Medetomidine hydrochloride can cause peripheral vasoconstriction through the activation of α2 adrenoceptors on blood vessels .
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1
1 Cited Publications
Cat. No.: HY-12707
CAS No.: 3605-01-4
Purity:  99.33%
Piribedil is a potent and orally active dopamine D2 and dopamine D3 agonist. Piribedil is also a α2-adrenoceptors antagonist. Piribedil can inhibit MLL1 methyltransferase activity (EC50: 0.18 μM). Piribedil has the potential for the research of parkinson's disease, circulatory disorders, cancers .
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1
1 Cited Publications
Cat. No.: HY-N3198A
CAS No.: 6882-66-2
Synonyms: (-)-Sophoramine
Sophoramine ((-)-Sophoramine) is a prejunctional α2-adrenoceptor inhibitor that can be found in the seeds of Sophora alopecuroides. Sophoramine inhibits prejunctional α2-adrenoceptors to facilitate norepinephrine release from adrenergic nerves. Sophoramine shows cytotoxic activity against human cancer cells, positive inotropic activity, and activity in rodent arrhythmia models. Sophoramine can be used for the research of arrhythmias .
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Cat. No.: HY-N1163
CAS No.: 6474-90-4
Synonyms: (-)-Tetrahydroalstonine
Tetrahydroalstonine ((-)-Tetrahydroalstonine) is an indole alkaloid and a selective α₂-adrenergic receptor antagonist. Tetrahydroalstonine exhibits certain neuroprotective effects. Tetrahydroalstonine can regulate autophagy-lysosomal function by activating the Akt/mTOR pathway, significantly reducing OGD/R-induced primary cortical neuronal injury .
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Cat. No.: HY-100490
CAS No.: 54187-04-1
Purity:  ≥99.0%
Rilmenidine, an innovative antihypertensive agent, is an orally active, selective I1 imidazoline receptor agonist. Rilmenidine is an alpha 2-adrenoceptor agonist. Rilmenidine induces autophagy. Rilmenidine acts both centrally by reducing sympathetic overactivity and in the kidney by inhibiting the Na +/H + antiport. Rilmenidine modulates proliferation and stimulates the proapoptotic protein Bax thus inducing the perturbation of the mitochondrial pathway and apoptosis in human leukemic K562 cells .
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Cat. No.: HY-100490B
CAS No.: 85409-38-7
Purity:  ≥98.0%
Rilmenidine phosphate, an innovative antihypertensive agent, is an orally active, selective I1 imidazoline receptor agonist. Rilmenidine phosphate is an alpha 2-adrenoceptor agonist. Rilmenidine phosphate induces autophagy. Rilmenidine phosphate acts both centrally by reducing sympathetic overactivity and in the kidney by inhibiting the Na +/H + antiport. Rilmenidine phosphate modulates proliferation and stimulates the proapoptotic protein Bax thus inducing the perturbation of the mitochondrial pathway and apoptosis in human leukemic K562 cells .
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Cat. No.: HY-109075A
CAS No.: 1465908-73-9
Purity:  99.32%
Target:  

Adrenergic Receptor

Research Areas:  

Neurological Disease

Tasipimidine sulfate is an orally active and selective α2A-adrenoceptor agonist with a pEC50 of 7.57 for human α2A-adrenoceptors and an EC50 of 5.7 nM for rat α2-adrenoceptor. Tasipimidine sulfate can be utilized in research related to situational anxiety and fear .
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