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.

Items 51-63 of 63

  • (rac)-CHEMBL333994
    Cat. No.
    A59710

    (rac)-CHEMBL333994

    Synonyms: (rac)-FK-480

    (rac)-CHEMBL333994 is a potent Cholecystokinin A (CCK-A) receptor antagonist with an IC50 of 0.67 nM, demonstrating effective oral bioavailability. This compound selectively targets peripheral CCK receptors, making it valuable for studying mechanistic pathways involved in gastrointestinal disorders. Its ability to increase CCK mRNA levels positions (rac)-CHEMBL333994 as a useful tool in research aimed at understanding chronic pancreatitis and related conditions.

    1 mg
    $155.00
    2 mg
    $235.00
    All 3 sizes
  • DA-3934
    Cat. No.
    A59714

    DA-3934

    DA-3934 is a cholecystokinin (CCK)-B receptor antagonist that effectively inhibits gastric acid secretion. Through its mechanism of action, DA-3934 blocks Pentagastrin-induced gastric acid release in rat models. This compound is valuable for research applications focused on gastrointestinal physiology and the modulation of acid secretion pathways.

    25 mg
    $1,780.00
    50 mg
    $2,280.00
    All 3 sizes
  • VL-0395
    Cat. No.
    A59715

    VL-0395

    VL-0395 is a selective antagonist of the cholecystokinin receptor 1 (CCK1), demonstrating an IC50 of 0.197 μM in rat pancreatic acinar cells. This compound effectively inhibits CCK1-mediated signaling pathways, making it a valuable tool for studying the physiological and pathological roles of CCK1 in digestive processes and pancreatic function. Its specificity and potency position VL-0395 as an essential reagent for research in gastrointestinal pharmacology and related fields.

    25 mg
    $1,275.00
    50 mg
    $1,625.00
    All 3 sizes
  • KSG-504 anhydrous
    Cat. No.
    A59716

    KSG-504 anhydrous

    KSG-504 anhydrous is a potent antagonist of the cholecystokinin (CCK) receptor. This compound has been shown to inhibit Ethionine-induced acute pancreatitis in rat models, demonstrating its relevance in studying pancreatic function and pathology. Additionally, KSG-504 facilitates the regeneration of acinar cells, making it a valuable tool for investigating therapeutic strategies in pancreatic diseases.

    25 mg
    $1,275.00
    50 mg
    $1,625.00
    All 3 sizes
  • TP-680
    Cat. No.
    A59719

    TP-680

    TP-680 is a potent cholecystokinin receptor antagonist, exhibiting a 1510-fold higher binding affinity for rat pancreatic CCKA receptors (IC50 = 1.2 nM) compared to rat brain CCKB receptors (IC50 = 1812.5 nM). This selectivity makes TP-680 a valuable tool for investigating gastrointestinal diseases. Its ability to modulate CCK receptor activity provides insights into gastrointestinal physiology and potential therapeutic applications in disorders related to CCK signaling.

    25 mg
    $1,275.00
    50 mg
    $1,625.00
    All 3 sizes
  • Asperlicin
    Cat. No.
    A59720

    Asperlicin

    Asperlicin is a cholecystokinin antagonist derived from Aspergillus alliaceus. This compound exhibits inhibitory effects on cholecystokinin receptors, which play a crucial role in regulating gastrointestinal functions and satiety. Asperlicin is primarily utilized in research related to digestive disorders, appetite regulation, and the study of neuropeptide signaling pathways. Its ability to modulate cholecystokinin activity makes it a valuable tool for understanding gastrointestinal and metabolic processes.

    Out of stock

    All 3 sizes
  • L-736380
    Cat. No.
    A59721

    L-736380

    L-736380 is a potent antagonist of the cholecystokinin B (CCK-B) receptor, exhibiting a high affinity with an IC50 of 0.054 nM for CCK-B and 400 nM for CCK-A. This compound effectively inhibits gastric acid secretion in anesthetized rats with an ID50 of 0.064 mg/kg. Additionally, L-736380 demonstrates significant activity in ex vivo binding assays of [125I]CCK-8S in BKTO mouse brain membranes, with an ED50 of 1.7 mg/kg. Its function as a CCK-B antagonist makes it a valuable tool for studies related to gastrointestinal physiology and neuropharmacology.

    25 mg
    $1,780.00
    50 mg
    $2,280.00
    All 3 sizes
  • CCK antagonist 1
    Cat. No.
    A59722

    CCK antagonist 1

    CCK Antagonist 1 is a potent antagonist of cholecystokinin (CCK) receptors, exhibiting IC50 values of 1.1 μM for CCK1 and 4 μM for CCK2. This compound is valuable for research into the roles of CCK in cancer and mental health disorders, facilitating the exploration of therapeutic interventions targeting these pathways. Its specificity and efficacy make it a useful tool for studying the biological functions of CCK receptors.

    1 mg
    $25.00
    5 mg
    $65.00
    All 7 sizes
  • S-0509
    Cat. No.
    A59723

    S-0509

    S-0509 is a selective antagonist of the CCKB/gastrin receptor, demonstrating potent inhibition of gastric secretion. This compound exhibits strong anti-secretory properties, making it a valuable tool in studies related to gastrointestinal health. S-0509 is particularly useful for research focused on the prevention of duodenal ulcers and the modulation of gastric acid secretion.

    Out of stock

    All 3 sizes
  • LY219057
    Cat. No.
    A59724

    LY219057

    LY219057 is a potent antagonist of cholecystokinin octapeptide (CCK-8), exhibiting an ID50 of 287.5 nM. This compound interferes with CCK-8 signaling pathways, making it valuable for investigating gastrointestinal and central nervous system functions. Its application spans research into appetite regulation, digestive processes, and potential therapeutic strategies for related disorders.

    25 mg
    $1,275.00
    All 1 sizes
  • PD-140548
    Cat. No.
    A59725

    PD-140548

    PD-140548 is a selective cholecystokinin (CCK-A) receptor antagonist, which plays a pivotal role in modulating neuropeptide signaling. This compound has demonstrated potential in the investigation of schizophrenia and related neuropsychiatric disorders, offering insights into the CCK system's influence on behavioral outcomes. Its specificity makes it a valuable tool for elucidating the role of CCK-A receptors in various biological processes.

    25 mg
    $1,530.00
    50 mg
    $1,950.00
    All 3 sizes
  • AG-041R
    Cat. No.
    A59726

    AG-041R

    AG-041R is a selective antagonist of the CCK2 receptor and functions as a gastrin inhibitor. It effectively inhibits gastrin-induced secretion of pancreastatin with an IC50 of 2.2 nM. Additionally, AG-041R demonstrates significant anti-proliferative effects on Mastomys ECL carcinoid tumor cells, making it a valuable tool for research applications related to gastrointestinal physiology and cancer biology.

    1 mg
    $120.00
    5 mg
    $560.00
    All 2 sizes
  • Gastrin/CCK antagonist 1
    Cat. No.
    A59728

    Gastrin/CCK antagonist 1

    Gastrin/CCK Antagonist 1 is a selective antagonist of the cholecystokinin receptor (CCK). This compound plays a significant role in inhibiting the action of gastrin and CCK, making it a valuable tool for studying gastrointestinal disorders. Research applications include evaluating gastrointestinal motility, secretion, and potential therapeutic approaches for conditions associated with dysregulated CCK signaling.

    1 mg
    $560.00
    5 mg
    $1,475.00
    All 2 sizes

Items 51-63 of 63

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