CCK

Cholecystokinin receptors (CCKRs) are a class of G-protein coupled receptors that respond to the peptide hormone cholecystokinin (CCK). CCK is predominantly found in the gastrointestinal tract and the central nervous system. There are two primary subtypes of cholecystokinin receptors: CCK-A (CCK1) receptor, mainly located in the pancreas, gallbladder, stomach, and certain areas of the brain, and CCK-B (CCK2) receptor, found predominantly in the brain and the stomach lining.

The primary function of CCKRs is to mediate the physiological actions of CCK. In the digestive system, CCK is involved in stimulating the digestion of fats and protein. It achieves this by inducing the secretion of digestive enzymes from the pancreas and bile from the gallbladder. Moreover, CCK plays a crucial role in regulating appetite by promoting satiety, making it a point of interest in obesity research.

In the central nervous system, CCK is involved in various functions, including anxiety, pain, and neuroendocrine control. CCK and its receptors are also implicated in psychiatric disorders like anxiety and panic attacks.

CCKRs are also significant in the medical field as potential targets for therapeutic intervention. For instance, CCK-B antagonists are being explored for their potential in treating anxiety disorders and gastrointestinal issues.

Overall, cholecystokinin receptors are integral to various physiological processes, from digestion to brain function, highlighting their importance in both understanding bodily functions and developing medical treatments.

10 Items

per page
Set Descending Direction
目录号
产品名
应用
产品描述
文献引用
  1. CCK-A receptor antagonist

    Loxiglumide (CR1505) 是一种胆囊收缩素拮抗剂
  2. CCK-2 receptor antagonist

    Z-360 是一种选择性的、可口服的、1,5-苯二氮䓬衍生物,是胃泌素/胆囊收缩素2(CCK-2)受体拮抗剂,具有潜在的抗肿瘤活性。
  3. CCK antagonist

    普鲁格鲁胺钠盐是一种非选择性胆囊收缩素(CCK)拮抗剂。它抑制CCK刺激的淀粉酶分泌,并防止CCK诱导的2-脱氧葡萄糖在小鼠胰腺泡中的摄取。
  4. CCK-2 receptor antagonist

    Nastorazepide 是一种选择性的、可口服的、1,5-苯二氮䓬衍生物 胃泌素/胆囊收缩素2(CCK-2)受体拮抗剂,具有潜在的抗肿瘤活性。
  5. CCK antagonist

    Proglumide 是一种药物,具有抑制胃分泌和减少胃肠蠕动的作用。Proglumide 是已知的胆囊收缩素(CCK)拮抗剂。
  6. Sincalide,也被称为 CCK-8,是一种用于治疗胆囊炎的药物。Sincalide 是一种存在于肠道和大脑中的八肽激素。当它从胃粘膜分泌时,它会刺激胆囊释放胆汁和胰腺释放消化酶。
  7. CCKA receptor antagonist

    Dexloxiglumide 是一种选择性的胆囊收缩素A型(CCKA)受体拮抗剂。Dexloxiglumide 是 Loxiglumide 的活性对映体,能够抑制由胆囊收缩素八肽(CCK-8)引起的平滑肌细胞收缩。
  8. nonpeptide cholecystokinin 1 receptor agonist

    SR 146131 是一种强效的、可口服的、选择性的非肽(胆囊收缩素1)受体激动剂。
  9. cholecystokinin 1 receptor agonist

    GI 181771 是一种胆囊收缩素1受体激动剂,正在研究用于治疗肥胖症。
  10. Gastrin/CCK-B antagonist

    Sograzepide(Netazepide;YF 476;YM-220)是一种极其强效、高度选择性且口服活性的胃泌素/CCK-B拮抗剂,具有0.1 nM的IC50值,对胃泌素/CCK-A活性具有抑制作用,其IC50为502 nM。

10 Items

per page
Set Descending Direction
苏ICP备14027875号-1