1. Signaling Pathways
  2. Neuropeptide S Receptor

Neuropeptide S Receptor (神经肽 S 受体)

Neuropeptide S Receptor; NPSR; GPR154; Vasopressin receptor-related receptor 1; VRR1

神经肽 S 受体 (NPSR) 是 G 蛋白偶联受体 (GPCR) 超家族的成员,是神经肽 S (NPS) 的特异性受体。NPSR 与 NPS 结合时具有高亲和力,可激活 Gq 和 Gs 蛋白,导致细胞内钙水平升高和环磷酸腺苷 (cAMP) 积累。NPSR 主要在与焦虑和应激反应相关的大脑区域表达,包括杏仁核复合体、室旁下丘脑核和海马体。该受体在各种生理过程中发挥重要作用,包括炎症、痛觉、运动活动、觉醒、焦虑调节和食物摄入,尤其与哮喘的发病机制有关

Neuropeptide S Receptor (NPSR) is a member of the G protein-coupled receptor (GPCR) superfamily and serves as the specific receptor for neuropeptide S (NPS). Upon binding to NPS, which occurs with high affinity, NPSR activates both Gq and Gs proteins, resulting in increased intracellular calcium levels and cyclic adenosine monophosphate (cAMP) accumulation. NPSR is predominantly expressed in brain regions associated with anxiety and stress responses, including the amygdaloid complex, paraventricular hypothalamic nucleus, and hippocampus. This receptor plays significant roles in various physiological processes, including inflammation, nociception, locomotor activity, wakefulness, anxiety regulation, and food intake, and is particularly implicated in the pathogenesis of asthma[1][2].

Neuropeptide S Receptor 相关产品 (2):

Cat. No. Product Name Effect Purity Chemical Structure
  • HY-108625
    SHA 68 Antagonist 99.84%
    SHA 68 是一种有效的选择性非肽神经肽 S 受体 (NPSR) 拮抗剂,对 NPSR Asn107 和 NPSR Ile107IC50 分别为 22.0 和 23.8 nM。SHA 68 具有有限的血脑屏障 (BBB) 渗透能力和用于神经痛的活性。
    SHA 68
  • HY-P1437A
    Neuropeptide S(Mouse) TFA Agonist
    Neuropeptide S(Mouse) TFA 是一种有效的内源性神经肽 S 受体 (NPSR) 激动剂 (EC50=3 nM)。 Neuropeptide S(Mouse) TFA 可诱导细胞内 Ca2+ 的动员。Neuropeptide S(Mouse) TFA 可以增加小鼠的运动活性和清醒度。Neuropeptide S(Mouse) TFA 还可以减少小鼠的焦虑样行为。
    Neuropeptide S(Mouse) TFA