1. Vías de señalización
  2. GPCR/G Protein
    Neuronal Signaling
  3. Adrenergic Receptor

Adrenergic Receptor

Beta Receptor

Adrenergic receptors are a class of G protein-coupled receptors that are targets of the catecholamines, especially norepinephrine and epinephrine. Many cells possess these receptors, and the binding of a catecholamine to the receptor will generally stimulate the sympathetic nervous system. The sympathetic nervous system is responsible for the fight-or-flight response, which includes widening the pupils of the eye, mobilizing energy, and diverting blood flow from non-essential organs to skeletal muscle. There are two main groups of adrenergic receptors, α and β, with several subtypes. α receptors have the subtypes α1 and α2. β receptors have the subtypes β1, β2 and β3. All three are linked to Gs proteins, which in turn are linked to adenylate cyclase. Agonist binding thus causes a rise in the intracellular concentration of the second messenger cAMP. Downstream effectors of cAMP include cAMP-dependent protein kinase (PKA), which mediates some of the intracellular events following hormone binding.

Cat. No. Nombre del producto Efecto Pureza Chemical Structure
  • HY-N14184
    Luminacin G1
    Luminacin G1 has a strong inhibitory effect on capillary formation (IC50 is less than 0.1 μg/mL).
    Luminacin G1
  • HY-W726392
    N-Nitrosometoprolol
    Inhibitor
    N-Nitrosometoprolol is an N-nitroso derivative formed by the in vitro reaction of β-adrenergic blockers with sodium nitrite. N-Nitrosometoprolol can induce micronuclei in rat liver, bone marrow and spleen.
    N-Nitrosometoprolol
  • HY-134125
    Yohimbic acid ethyl ester
    Antagonist
    Yohimbic acid ethyl ester (Compound 3a) is a selective ADRA2A antagonist with an IC50 of 31 nM.
    Yohimbic acid ethyl ester
  • HY-W722796
    Tuaminoheptane sulfate
    Agonist
    Tuaminoheptane sulfate is an alpha-adrenergic receptor agonist. Tuaminoheptane sulfate exerts its decongestant and irritant effects by inhibiting norepinephrine reuptake and promoting its release. Tuaminoheptane sulfate can be used in research on nasal diseases such as decongestion.
    Tuaminoheptane sulfate
  • HY-B0192AR
    Alfuzosin hydrochloride (Standard)
    Antagonist
    Alfuzosin (hydrochloride) (Standard) is the analytical standard of Alfuzosin (hydrochloride). This product is intended for research and analytical applications. Alfuzosin (SL 77499-10) hydrochloride is an orally active, selective and competitive α1-adrenoceptor antagonist. Alfuzosin hydrochloride relaxes the muscles of the prostate and bladder neck, aiding in urination. Alfuzosin hydrochloride can be used in study of benign prostatic hyperplasia (BPH).
    Alfuzosin hydrochloride (Standard)
  • HY-W752055
    (Rac)-Nebivolol-d4 hydrochloride
    Inhibitor
    (Rac)-Nebivolol-d4 hydrochloride is a labelled racemic Nebivolol. Nebivolol selectively inhibits β1-adrenergic receptor with an IC50 of 0.8 nM.
    (Rac)-Nebivolol-d<sub>4</sub> hydrochloride
  • HY-124208
    L-770644
    Agonist
    L-770644 is an orally active, potent and selective agonist of the human β3 adrenergic receptor (EC50 = 13 nM).
    L-770644
  • HY-B1506AS
    Acepromazine-d6maleate
    Antagonist
    Acepromazine-d6 (maleate) (Acetopromazine-d6 (maleate)) is deuterium labeled Acepromazine (maleate). Acepromazine (Acetopromazine) maleate is a phenothiazine tranquilizer and is alpha-adrenoceptor antagonist.
    Acepromazine-d<sub>6</sub>maleate
  • HY-N14033
    Luminacin C1
    Luminacin C1 has a strong inhibitory effect on capillary formation (IC50 is less than 0.1 μg/mL).
    Luminacin C1
  • HY-17503D
    Metoprolol Hydrochloride
    Antagonist
    Metoprolol Hydrochloride is an orally active and selective β1-adrenoceptor antagonist. Metoprolol Hydrochloride exhibits anti-inflammatory, antitumor, and anti-angiogenic properties.
    Metoprolol Hydrochloride
  • HY-123514
    SNAP8719 free base
    Antagonist
    SNAP8719 free base is a selective α1D-adrenoceptor antagonist (pKi = 8.89). SNAP8719 free base shows affinity for the dopamine D2-, 5-HT1A-, and the human clonal α2a-adrenoceptor, with pKi values of 5.98, 6.47, and <5.0, respectively. SNAP8719 free base causes a concentration-dependent increase in the twitch response.
    SNAP8719 free base
  • HY-105672
    Cafaminol
    Cafaminol (Methylcoffanolamine) is a vasoconstrictor and anticatarrhal that selectively binds to alpha-1 receptors, causing blood vessels to constrict. Cafaminol is an xanthine derivative which can be utilized in decongestant and antitumor research.
    Cafaminol
  • HY-119456AS
    Romifidine-d4 hydrochloride
    Romifidine-d4 (hydrochloride) is the deuterium labeled Romifidine hydrochloride.
    Romifidine-d<sub>4</sub> hydrochloride
  • HY-A0008R
    Talipexole dihydrochloride (Standard)
    Agonist
    Talipexole (dihydrochloride) (Standard) is the analytical standard of Talipexole (dihydrochloride). This product is intended for research and analytical applications. Talipexole dihydrochloride (B-HT 920 dihydrochloride) is a dopamine D2 receptor agonist, α2-adrenoceptor agonist and 5-HT3 receptor antagonist, which displays antiParkinsonian activity.
    Talipexole dihydrochloride (Standard)
  • HY-122120
    Rafabegron
    Rafabegron (AJ-9677) is a specific beta3-adrenoceptor agonist. Rafabegron can reduce blood glucose, insulin, FFA, and triglyceride levels in diabetic and obese mouse models.
    Rafabegron
  • HY-103212
    Azepexole dihydrochloride
    Agonist
    Azepexole (B-HT 933) dihydrochloride is a potent and selective alpha 2-adrenoceptor agonist with pKis of 8.3, 7.6, and 7.5 for α2A-, α2B- and α2C-adrenoceptor subtypes, resepctively. Azepexole dihydrochloride causes concentration-dependent inhibition of peristaltic contractions (IC50= 78.72 nM).
    Azepexole dihydrochloride
  • HY-17416S2
    Guanfacine-13C,d5 hydrochloride
    Agonist
    Guanfacine-13C,d5 hydrochloride is the deuterium and 13C labeled Guanfacine hydrochloride (HY-17416). Guanfacine hydrochloride is an orally active noradrenergic α2A agonist and has high selective for the α2A receptor subtype. Guanfacine has effects in producing hypotension and sedation. Guanfacine can be used for the research of a variety of prefrontal cortex (PFC) cognitive disorders, including tourette's syndrome and attention deficit hyperactivity disorder (ADHD).
    Guanfacine-<sup>13</sup>C,d<sub>5</sub> hydrochloride
  • HY-B0381BR
    Levobetaxolol hydrochloride (Standard)
    Inhibitor
    Levobetaxolol (hydrochloride) (Standard) is the analytical standard of Levobetaxolol (hydrochloride). This product is intended for research and analytical applications.
    Levobetaxolol hydrochloride (Standard)
  • HY-121692B
    (S)-Alprenolol hydrochloride
    Inhibitor
    (S)-Alprenolol hydrochloride is a potent and nonselective β-blocker.
    (S)-Alprenolol hydrochloride
  • HY-B0432R
    Propafenone (Standard)
    Antagonist
    Propafenone (Standard) is the analytical standard of Propafenone. This product is intended for research and analytical applications. Propafenone (SA-79), a sodium-channel blocker, acts an antiarrhythmic agent. Propafenone also has high affinity for the β receptor (IC50=32 nM). Propafenone blocks the transient outward current (Ito) and the sustained delayed rectifier K current (Isus) with IC50 values of 4.9 μm and 8.6 μm, respectively. Propafenone suppresses esophageal cancer proliferation through inducing mitochondrial dysfunction and induce apoptosis.
    Propafenone (Standard)
Cat. No. Nombre del producto / Synonyms Application Reactivity

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