1. Signaling Pathways
  2. GPCR/G Protein
    Neuronal Signaling
  3. Cholecystokinin Receptor

Cholecystokinin Receptor (胆囊收缩素受体)

CCK Receptor

Cholecystokinin receptors are a group of G-protein coupled receptors which bind the peptide hormones cholecystokinin (CCK) and gastrin. Two types of functional membrane receptors, cholecystokinin A receptor (CCK-AR), located mainly on pancreatic acinar cells, and CCK-BR, mostly in the stomach and nervous system tissues, have been identified as the endogenous receptors of CCK. Both have high affinity for the sulfated CCK octapeptide (CCK-8), whereas only the CCK-BR has high affinity for gastrin.

CCK is a peptide hormone discovered in the small intestine. Together with secretin and gastrin, CCK constitutes the classical gut hormone triad. In addition to gallbladder contraction, CCK also regulates pancreatic enzyme secretion and growth, intestinal motility, satiety signalling and the inhibition of gastric acid secretion. CCK is also a transmitter in central and intestinal neurons.

Cholecystokinin Receptor 相关产品 (50):

Cat. No. Product Name Effect Purity Chemical Structure
  • HY-160045
    AP1153 aptamer sodium Chemical
    AP1153 aptamer sodium 是特异性结合胆囊收缩素受体 CCKBR 的 DNA 适体 (Kd: ~15 pM),但不激活 CCKBR 相关信号通路。AP1153 aptamer sodium 以受体介导的方式被胰腺导管腺癌 (PDAC) 细胞内化。AP1153 aptamer sodium 可以与荧光纳米颗粒表面发生生物共轭,在体内促进纳米颗粒递送至 PDAC 肿瘤。
    AP1153 aptamer sodium
  • HY-103354A
    Proglumide hemicalcium

    丙谷胺钙盐

    Antagonist
    Proglumide hemicalcium 是一种非肽和口服活性胆囊收缩素 (CCK)-A/B 受体拮抗剂。Proglumide hemicalcium 选择性阻断 CCK 在中枢神经系统中的作用。Proglumide hemicalcium 具有抑制胃分泌和保护胃十二指肠粘膜的能力,还具有抗癫痫和抗氧化活性。
    Proglumide hemicalcium
  • HY-162070
    CCK antagonist 1 Antagonist 99.96%
    CCK antagonist 1 (compound 3d) 是 CCK 拮抗剂,对 CCK1 和 CCK2 的 IC50s 分别为 1.1 μM 和 4 μM。CCK antagonist 1 可用于癌症和精神疾病的研究。
    CCK antagonist 1
  • HY-125314
    AG-041R Antagonist
    AG-041R 是一种有效的选择性的 CCK2 受体/胃泌素 (CCK2 Receptor/Gastrin) 拮抗剂。AG-041R 抑制胃泌素诱导的胰抑素分泌,其 IC50 为 2.2 nM。AG-041R 抑制 Mastomys ECL 类癌细胞的生长。
    AG-041R
  • HY-U00062
    Tarazepide

    他折派特

    Antagonist
    Tarazepide 是一种有效且特异性的 CCK-A 受体拮抗剂。
    Tarazepide
  • HY-U00363
    CHEMBL333994 Antagonist
    CHEMBL333994 是一种有口服活性的,缩胆囊素 A (CCK-A) 的有效拮抗剂,其 IC50 值为 0.67 nM。
    CHEMBL333994
  • HY-11076
    GI 181771 Agonist
    GI 181771是用于研究肥胖症的胆囊收缩素1 (cholecystokinin 1) 受体激动剂。
    GI 181771
  • HY-P1593
    Mini Gastrin I, human
    Mini Gastrin I, human 为由 13 个氨基酸组成的短的人胃泌素 (gastrin)。
    Mini Gastrin I, human
  • HY-U00387
    CCK-A receptor inhibitor 1 Inhibitor
    CCK-A receptor inhibitor 1 是一种缩胆囊素 A (cholecystokinin A, CCK-A) 受体抑制剂,IC50 为 340 nM。
    CCK-A receptor inhibitor 1
  • HY-U00375
    Gastrin/CCK antagonist 1 Antagonist
    Gastrin/CCK antagonist 1 是 gastrin/CCK 的拮抗剂,可用于肠胃失调疾病的研究。
    Gastrin/CCK antagonist 1