1. Signaling Pathways
  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. Product Name Effect Purity Chemical Structure
  • HY-14541S1
    Olanzapine-d4
    Antagonist
    Olanzapine-d4 (LY170053-d4) is deuterium-labeled Olanzapine (HY-14541).
    Olanzapine-d<sub>4</sub>
  • HY-106973A
    Nolomirole hydrochloride
    Agonist
    Nolomirole (CHF 1035) hydrochloride is an orally active and selective DA2 dopaminergic receptor/α2-adrenoceptor agonist. Nolomirole attenuates the heart failure signs in the Monocrotaline (HY-N0750)-induced congestive heart failure model. Nolomirole increases cardiac output.
    Nolomirole hydrochloride
  • HY-B0010E
    Arformoterol maleate
    Agonist
    Arformoterol ((R,R)-Formoterol) maleate, the (R,R)-enantiomer of Formoterol, is a long-acting β2-adrenergic receptor (β2-AR) agonist, with a Kd of 2.9 nM. Arformoterol maleate can be used for the research of chronic obstructive pulmonary disease (COPD).
    Arformoterol maleate
  • HY-167689
    Parethoxycaine hydrochloride
    Parethoxycaine hydrochloride is an anesthetic with nerve conduction blocking activity. Parethoxycaine hydrochloride exhibits non-selective inhibitory effects on responses to various stimulants in rat vas deferens and guinea pig ileum muscles. Parethoxycaine hydrochloride has an enhanced effect on the action of norepinephrine, and its methyl bromide derivative also exhibits the same properties on the action of norepinephrine and potassium ions. Derivatives of parethoxycaine hydrochloride have significant effects on calcium dose-response curves, displaying different tissue and stimulant selectivities. The mechanism of action of Parethoxycaine hydrochloride involves the regulation of calcium transport processes.
    Parethoxycaine hydrochloride
  • HY-17495AR
    Carteolol hydrochloride (Standard)
    Antagonist
    Carteolol hydrochloride (Standard) is the analytical standard of Carteolol hydrochloride. This product is intended for research and analytical applications. Carteolol hydrochloride (OPC-1085 hydrochloride) is a non-selective beta blocker used to treat glaucoma.
    Carteolol hydrochloride (Standard)
  • HY-B1347R
    Clorprenaline hydrochloride (Standard)
    Agonist
    Clorprenaline hydrochloride (Standard) is the analytical standard of Clorprenaline hydrochloride. This product is intended for research and analytical applications. Clorprenaline hydrochloride is a β2-adrenergic receptor agonist that is implicated in bronchial expansion. Clorprenaline has the potential for asthma research.
    Clorprenaline hydrochloride (Standard)
  • HY-15413
    Edivoxetine
    Inhibitor
    Edivoxetine is a selective and potent norepinephrine reuptake inhibitor (NERI) being used in depressive disorder or attention-deficit/hyperactivity disorder.
    Edivoxetine
  • HY-W714108
    Metrazoline
    Ligand
    Metrazoline (o-Methyl-tracizoline) is the ligand for adrenergic receptor (low affinity) and imidazoline I2 receptor.
    Metrazoline
  • HY-B0371AR
    Terazosin (hydrochloride dihydrate) (Standard)
    Antagonist
    Terazosin (hydrochloride dihydrate) (Standard) is the analytical standard of Terazosin (hydrochloride dihydrate). This product is intended for research and analytical applications. Terazosin hydrochloride dihydrate is a quinazoline derivative and a competitive and orally active α1-adrenoceptor antagonist. Terazosin hydrochloride dihydrate works by relaxing blood vessels and the opening of the bladder. Terazosin hydrochloride dihydrate has the potential for benign prostatic hyperplasia (BPH) and high blood pressure treatment.
    Terazosin (hydrochloride dihydrate) (Standard)
  • HY-117071A
    Dabuzalgron hydrochloride
    Agonist
    Dabuzalgron (Ro 115-1240) hydrochloride is an orally active and selective α-1A adrenergic receptor agonist for the treatment of urinary incontinence. Dabuzalgron hydrochloride protects against Doxorubicin-induced cardiotoxicity by preserving mitochondrial function.
    Dabuzalgron hydrochloride
  • HY-126107
    (±)-4-Hydroxy propranolol β-D-glucuronide
    Control
    (±)-4-Hydroxy propranolol β-D-glucuronide is a metabolite of the β-adrenergic receptor antagonist 4-Hydroxypropranolol (HY-100634).
    (±)-4-Hydroxy propranolol β-D-glucuronide
  • HY-W741999
    Metaproterenol-d7-1 hemisulfate
    Agonist
    Metaproterenol-d7-1 (hemisulfate) is deuterium labeled Metaproterenol (hemisulfate). Metaproterenol hemisulfate (Orciprenaline hemisulfate) is a direct-acting sympathomimetic and a β2-adrenergic receptor (β2AR) agonist with an IC50 of 68 nM. Metaproterenol hemisulfate also has anti-inflammatory activity.
    Metaproterenol-d<sub>7</sub>-1 hemisulfate
  • HY-106769B
    (3aR,9aR)-Fluparoxan
    (3aR,9aR)-Fluparoxan ((3aR,9aR)-GR50360) is a highly selective and potent α2B adrenaline receptor antagonist with the activity of preventing, improving or inhibiting neurodevelopmental disorders and neurodegenerative diseases. As an α2B receptor antagonist, (3aR,9aR)-Fluparoxan can promote the recovery of neurological function. The mechanism of action of (3aR,9aR)-Fluparoxan makes it have important application potential in neuroscience research.
    (3aR,9aR)-Fluparoxan
  • HY-W042920A
    TDIQ hydrochloride
    Ligand
    TDIQ hydrochloride is an analog of Amphetamine with high affinity for α2-adrenergic receptor. TDIQ hydrochloride is a selective α2-adrenoceptor ligand with the Ki values of 75 nM, 95 nM, and 65 nM for α2A-, α2B-, and α2C-adrenergic receptors, respectively.
    TDIQ hydrochloride
  • HY-107327R
    Carazolol (Standard)
    Antagonist
    Carazolol (Standard) is the analytical standard of Carazolol. This product is intended for research and analytical applications. Carazolol is a β12 adrenoceptor antagonist of high potency used in the research of hypertension. Carazolol is also a potent, selective β3-adrenoceptor agonist.
    Carazolol (Standard)
  • HY-W103372
    Vasorelaxant agent-2
    Modulator
    Vasorelaxant agent-2 (Compound 8h) targets α1A-adrenergic receptor with an affinity of pD2=5.4. Vasorelaxant agent-2 exhibits vasodilator activity in rats aortic rings with an EC50 of 0.79 μM.
    Vasorelaxant agent-2
  • HY-103201
    A 80426 mesylate
    Antagonist
    A 80426 mesylate is an α2-adrenoceptor antagonist. A 80426 mesylate is used in antidepressant research.
    A 80426 mesylate
  • HY-B0938
    Mephentermine hemisulfate
    Mephentermine is a sympathomimetic amine, frequently used as a vasopressor.
    Mephentermine hemisulfate
  • HY-121692A
    (S)-Alprenolol L-tartrate
    Antagonist
    (S)-Alprenolol is a potent and nonselective β-adrenoceptor antagonist.
    (S)-Alprenolol L-tartrate
  • HY-101752A
    (±)-Befunolol hydrochloride
    Inhibitor
    (±)-Befunolol hydrochloride is a β-adrenoceptor blocking agent.
    (±)-Befunolol hydrochloride
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