1. GPCR/G Protein
  2. Adrenergic Receptor

Adrenergic 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.

Adrenergic Receptor 相关产品 (174):

Cat. No. Product Name Effect Purity
  • HY-B0468
    Isoprenaline hydrochloride Agonist >99.0%
    Isoprenaline hydrochloride是一种非选择性的β-肾上腺素能受体激动剂,具有有效的外周血管扩张剂,支气管扩张剂和心脏刺激活性。
  • HY-13715B
    Norepinephrine bitartrate monohydrate Agonist 99.75%
    Norepinephrine bitartrate monohydrate 是β1-选择性的肾上腺素能受体激动剂,EC50 为 5.37 μM。
  • HY-B0573
    Propranolol hydrochloride Antagonist 99.92%
    Propranolol hydrochloride是一种非选择性β-肾上腺素能受体(βAR)拮抗剂, IC50 值为12 nM。
  • HY-13951
    ICI 118,551 hydrochloride Antagonist 98.50%
    ICI 118,551 hydrochloride 是一种高度选择性的 β2 adrenergic receptor 拮抗剂,能够作用于β2,β1 和 β3 受体,Ki 值分别为 0.7,49.5 和 611 nM。
  • HY-B0471
    (R)-(-)-Phenylephrine hydrochloride Agonist 98.10%
    (R)-(-)-Phenylephrine hydrochloride是一种选择性的α1-肾上腺素能受体激动剂,对α1D,α1B 和α1A 受体的pKis 分为5.86,4.87和4.70。
  • HY-B0447B
    L-Epinephrine Agonist >99.0%
    L-Epinephrine是由肾上腺髓质分泌的激素。它是α-adrenergicβ-adrenergic受体激动剂。
  • HY-19057A
    Vatinoxan hydrochloride Antagonist 99.25%
    Vatinoxan hydrochloride (MK-467hydrochloride;L-659066 hydrochloride) 是一种外周 α2 肾上腺素能受体 (α2 adrenergic receptor) 拮抗剂。
  • HY-101385
    L-765314 Agonist
    L-765314 是 α1b 肾上腺素能受体 (α1b adrenergic receptor) 的一个有效的、选择性拮抗剂,其在大鼠和人体中的 Ki 值分别为 5.4 nM 和 2.0 nM。
  • HY-N0127
    Yohimbine Hydrochloride Antagonist 99.85%
    Yohimbine hydrochloride 是α-2肾上腺素能受体抑制剂,阻断突触前或突触后的α-2肾上腺素能受体,引起去甲肾上腺素和多巴胺的释放。
  • HY-14773
    Mirabegron Agonist 99.08%
    Mirabegron 是一种选择性的肾上腺素受体 (β3-adrenoceptor) 激动剂,EC50 为 22.4 nM。
  • HY-B0193A
    Prazosin hydrochloride Antagonist 99.73%
    Prazosin盐酸盐是α肾上腺素阻断剂,可作用于高血压、焦虑和恐慌症等。
  • HY-B0162A
    Ivabradine hydrochloride Inhibitor 98.39%
    Ivabradine hydrochloride 是一个新颖的 If 抑制剂,IC50值为 2.9 μM,用于降低心率。
  • HY-B0362A
    Phentolamine mesylate Antagonist 99.83%
    Phentolamine mesylate是竞争性,可逆的 α-肾上腺素能受体 拮抗剂,IC50 在5和30 nM之间。
  • HY-B0437
    Sotalol hydrochloride Antagonist 99.77%
    Sotalol盐酸盐是肾上腺素受体拮抗剂,可作用于威胁生命的心律失常。
  • HY-17416
    Guanfacine hydrochloride Agonist 99.64%
    Guanfacine盐酸盐是α2A肾上腺素受体激动剂,Kd为31 nM,具有抗高血压的活性。
  • HY-B0006
    Carvedilol Inhibitor 99.93%
    Carvedilol(BM14190)是非选择性β和α1阻断剂,能抑制LDL的氧化,IC50为3.8 μM。
  • HY-B1614
    Clenbuterol hydrochloride Agonist 99.23%
    Clenbuterol hydrochloride是β2 adrenergic受体激动剂。它是一种强效的支气管扩张剂,具有脂肪燃烧性能。
  • HY-B0802
    Terbutaline sulfate Agonist >98.0%
    Terbutaline硫酸盐是肾上腺素能受体_beta_2激动剂。
  • HY-B0443A
    Xylazine hydrochloride Agonist 99.90%
    Xylazine盐酸盐是α2肾上腺素受体激动剂。
  • HY-17453
    Salmeterol xinafoate Agonist
    Salmeterol xinafoate 是长效 β2 肾上腺素能受体 (β2AR) 激动剂,对WT β2AR的Ki值为 1.5 nM。
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