1. Signaling Pathways
  2. GPCR/G Protein
  3. Neuromedin U Receptor (NMUR)

Neuromedin U Receptor (NMUR) (神经调节肽 U 受体)

Neuromedin U Receptor

神经调节肽 U 受体属于 G 蛋白偶联受体家族,归类为 Class A。神经调节肽 U 受体可与神经肽激素神经质素 U 和神经质素 S 结合。神经调节肽 U 受体包括 NMUR1 和 NMUR2,NMUR1 主要在胃肠道等外周组织表达,NmU-R2 主要在中枢神经系统表达。神经调节肽 U 受体能介导细胞内 Ca2+ 等信号转导,调节胃肠道、心血管、神经内分泌等多系统的生理功能,如影响平滑肌收缩、血压、摄食、能量平衡和应激反应等。神经调节肽 U 受体与癌症、疼痛、代谢性疾病、胃肠道疾病等的发生发展密切相关,是极具潜力的疾病治疗靶点[1]

Neuromedin U Receptor belongs to the G protein-coupled receptors family and is classified as Class A. Neuromedin U Receptor can bind the neuropeptide hormones neuromedin U and neuromedin S. Neuromedin U Receptor includes NMUR1 and NMUR2. NMUR1 is mainly expressed in peripheral tissues such as the gastrointestinal tract, while NmU-R2 is mainly expressed in the central nervous system. Neuromedin U Receptor can mediate intracellular signal transduction such as Ca2+ and regulate the physiological functions of multiple systems such as the gastrointestinal tract, cardiovascular system, and neuroendocrine system, for example, affecting smooth muscle contraction, blood pressure, feeding, energy balance, and stress responses. Neuromedin U Receptor is closely related to the occurrence and development of diseases such as cancer, pain, metabolic diseases, and gastrointestinal diseases, and is a highly potential target for disease treatment[1].

Neuromedin U Receptor (NMUR) 相关产品 (5):

Cat. No. Product Name Effect Purity Chemical Structure
  • HY-145086
    R-PSOP Antagonist 99.90%
    R-PSOP 是一种高效、选择性的非肽 NMUR2 拮抗剂。R-PSOP 与 NMUR2 结合,对人和大鼠 NMUR2 的 Ki 分别为 52 和 32 nM。R-PSOP 可中度通过血脑屏障。R-PSOP 可用于研究饮食障碍、肥胖、疼痛和应激相关障碍。
    R-PSOP
  • HY-P3030
    CPN-219 Agonist 98.13%
    CPN-219,一种新一代六肽类 NMUR2 激动剂,实现了对 NMUR2 的剂量依赖性和选择性激活,其 EC50 值为 2.2 nM.
    CPN-219
  • HY-P5084
    Neuromedin S (human) Modulator
    Neuromedin S (human) 是一种神经肽,含有 33 个氨基酸。Neuromedin S (human) 已在大脑中被鉴定为 G 蛋白偶联受体 (GPCR) FM-4/TGR-1 的内源性配体,并作用于神经调节素 U (NMU) 受体 2 (NMUR2) 调节体重稳态。
    Neuromedin S (human)
  • HY-P10473
    CPN-351 Antagonist
    CPN-351 (compound 9a) 是一种 hNMUR1 的选择性拮抗剂。CPN-351 可用于炎症和癌症的研究。
    CPN-351
  • HY-124681
    NY0116 Agonist
    NY0116 是一种神经调节肽 U 受体 2 (NMUR2) 激动剂,hNMUR1 的 EC50 值为 27.76 μM,hNMUR2 的 EC50 值为 13.61 μM。NY0116 降低 cAMP,同时刺激稳定表达 NMUR2 HEK293 细胞中的钙信号传导。
    NY0116