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-19401A
    L-796568 free base
    Agonist
    L-796568 free base is a β(3)-adrenergic receptor agonist. L-796568 free base can be used for the research of obesity.
    L-796568 free base
  • HY-106554A
    Trimazosin hydrochloride hydrate
    Inhibitor
    Trimazosin hydrochloride hydrate is an orally active, quinazoline derivative which is structurally related to prazosin. Trimazosin shows hypotensive effect by selectively block α1-adrenergic receptor.
    Trimazosin hydrochloride hydrate
  • HY-B0556AR
    Tetrahydrozoline hydrochloride (Standard)
    Agonist
    Tetrahydrozoline (hydrochloride) (Standard) is the analytical standard of Tetrahydrozoline (hydrochloride). This product is intended for research and analytical applications. Tetrahydrozoline hydrochloride (Tetryzoline hydrochloride), a derivative of imidazoline, is an α-adrenergic agonist that causes vasoconstriction. Tetrahydrozoline hydrochloride is widely used for the research of nasal congestion and conjunctival congestion.
    Tetrahydrozoline hydrochloride (Standard)
  • HY-B0661R
    Tamsulosin (Standard)
    Antagonist
    Tamsulosin (Standard) is the analytical standard of Tamsulosin. This product is intended for research and analytical applications. Tamsulosin ((R)-(-)-YM12617 free base) is an inhibitor of α1-adrenergic receptor. Tamsulosin is used for the research of prostatic hyperplasia. Tamsulosin attenuates abdominal aortic aneurysm growth in animal models.
    Tamsulosin (Standard)
  • HY-124208A
    L-770644 dihydrochloride
    Agonist
    L-770644 is an orally active, potent and selective agonist of the human β3 adrenergic receptor (EC50 = 13 nM).
    L-770644 dihydrochloride
  • HY-G0008AR
    O-Desmethyl Mebeverine alcohol hydrochloride (Standard)
    Diethyl phthalate (Standard) is the analytical standard of Diethyl phthalate. This product is intended for research and analytical applications. Diethyl phthalate is an endocrine disruptor that has the activity of affecting the apoptosis system of PC12 cells. Diethyl phthalate is widely used in a variety of plastics and personal care products. Diethyl phthalate has shown the potential to induce male reproductive toxicity unrelated to androgens in animal experiments.
    O-Desmethyl Mebeverine alcohol hydrochloride (Standard)
  • HY-U00303
    Trecadrine
    Agonist
    Trecadrine is a β3-adrenergic agonist.
    Trecadrine
  • HY-U00391
    β3-AR agonist 2
    Agonist
    β3-AR agonist 2 is a potent and selective β3-adrenergic receptor (β3-AR) agonist with an EC50 of 8 nM.
    β3-AR agonist 2
  • HY-101690
    QF0301B
    Antagonist
    QF0301B is an α1 adrenergic receptor antagonist and a low α2 adrenoceptor, 5-HT2A, and histamine H1 receptor blocker.
    QF0301B
  • HY-U00356
    Tertatolol
    Antagonist
    Tertatolol is a potent antagonist of beta-adrenoceptor and 5-HT receptor, with unique renal vasodilatatory effects.
    Tertatolol
  • HY-U00367
    (4E)-SUN9221
    Antagonist
    (4E)-SUN9221 is a potent antagonist of α1-adrenergic receptor and 5-HT2 receptor, with antihypertensive and anti-platelet aggregation activities.
    (4E)-SUN9221
  • HY-U00333
    α1 adrenoceptor-MO-1
    Modulator
    α1 adrenoceptor-MO-1, an S enantiomer, has affinity at alpha 1 adrenergic receptor, shows alphalytic activity, and possesses analgesic action; more active than R enantiomer.
    α1 adrenoceptor-MO-1
  • HY-U00206
    D2343
    Modulator
    D2343 is a β2-adrenoceptor agonist and also is an α1- adrenoceptor inhibitor.
    D2343
  • HY-U00183
    Epanolol
    Agonist
    Epanolol (Visacor; ICI141292) is a potent β-adrenoceptor partial agonist with a greater affinity for β1- than β2-adrenoceptors.
    Epanolol
  • HY-U00399
    Fiduxosin
    Antagonist
    Fiduxosin is a potent α1-adrenoceptor antagonist, with Ki of 0.160 nM, 24.9 nM, and 0.920 nM for α1a-, α1b-, and α1d-adrenoceptors, respectively.
    Fiduxosin
  • HY-U00110
    MG 1
    Antagonist
    MG 1 is an α1 adrenergic receptor antagonist.
    MG 1
  • HY-U00313
    Tropodifene
    Inhibitor
    Tropodifene (Tropaphen) is an α-Adrenergic receptor inhibitor.
    Tropodifene
  • HY-U00365
    5-HT2 antagonist 1
    Antagonist
    5-HT2 antagonist 1 is a potent antagonist of 5-HT2 receptor, with weak α1 adrenoceptor blocking activity.
    5-HT2 antagonist 1
  • HY-U00244
    Benzquinamide
    Inhibitor
    Benzquinamide (P2647) is an antiemetic which can bind to the α2A, α2B, and α2C adrenergic receptors (α2-AR) with Ki values of 1,365, 691, and 545 nM, respectively.
    Benzquinamide
  • HY-U00191
    GP2-114
    GP2-114 (GP-2-114) produces current-dependent cardiovascular action when administered by transdermal iontophoresis.
    GP2-114
Cat. No. Product Name / Synonyms Application Reactivity

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