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 76-100 of 105

  • CI-988
    Cat. No.
    A59701

    CI-988

    Synonyms: PD134308

    CI-988 is a potent and selective antagonist of the cholecystokinin 2 receptor (CCK2R), exhibiting an IC50 of 1.7 nM in mouse cortex assays. Demonstrating over 1600-fold selectivity for CCK2 over the CCK1 receptor, CI-988 has been shown to possess anxiolytic and anti-tumor properties. This compound is valuable for research into therapeutic applications in anxiety disorders and cancer treatment.

    5 mg
    $485.00
    10 mg
    $800.00
    All 2 sizes
  • Itriglumide
    Cat. No.
    A59702

    Itriglumide

    Synonyms: CR 2945

    Itriglumide is a potent and selective antagonist of the cholecystokinin B receptor (CCKBR), exhibiting an IC50 of 2.3 nM. It effectively antagonizes gastrin response in a dose-dependent manner, with an IC50 of 5.9 nM. Itriglumide demonstrates significant antisecretory and antiulcer properties, making it a valuable reagent for research in gastrointestinal pharmacology and related studies.

    1 mg
    $235.00
    2 mg
    $360.00
    All 6 sizes
  • Caerulein, desulfated
    Cat. No.
    A59703

    Caerulein, desulfated

    Caerulein, desulfated is a desulfurated form of the decapeptide Caerulein, which shares five carboxyl-terminal amino acids with gastrin and cholecystokinin (CCK). This compound primarily targets and activates CCK receptors, playing a significant role in gastrointestinal physiology. It is widely utilized in research applications focused on understanding digestive processes, appetite regulation, and modulation of pancreatic activities.

    1 mg
    $50.00
    5 mg
    $115.00
    All 6 sizes
  • FPL 14294
    Cat. No.
    A59704

    FPL 14294

    Synonyms: ARL 14294

    FPL 14294 is an intranasally active anorectic agent and cholecystokinin octapeptide (CCK) analog known for its enhanced metabolic stability. This compound effectively induces satiety across various species, making it a valuable tool for research in appetite regulation and metabolic studies. Its unique properties facilitate investigations into mechanisms of weight control and potential therapeutic interventions for obesity.

    Out of stock

    All 3 sizes
  • Cholecystokinin (1-21)
    Cat. No.
    A59705

    Cholecystokinin (1-21)

    Synonyms: CCK-1-21

    Cholecystokinin (1-21) is a fragment of the cholecystokinin polypeptide that primarily targets the CCK receptors. This peptide is known to stimulate lipolysis in human adipose tissue, making it an important reagent for studies focused on metabolic regulation and energy homeostasis. Its application extends to research involving appetite regulation and gastrointestinal function.

    Out of stock

    All 3 sizes
  • LY288513
    Cat. No.
    A59706

    LY288513

    LY288513 is a selective non-peptide antagonist of the cholecystokinin B (CCK-B) receptor, exhibiting an IC50 value of 16 nM. It has been demonstrated to produce anxiolytic-like effects in murine models, making it a valuable tool for research in anxiety disorders and related neurobiological studies. Its specificity for the CCK-B receptor allows for targeted investigation into the mechanisms underlying anxiety and stress responses.

    1 mg
    $200.00
    5 mg
    $515.00
    All 4 sizes
  • JMV 179
    Cat. No.
    A59707

    JMV 179

    JMV 179 is a cholecystokinin receptor (CKK) antagonist with an IC50 of 30 nM. This peptide analog is designed to inhibit CCK receptor activity, making it a valuable tool for studying the physiological and pathophysiological roles of CCK signaling. JMV 179 is utilized in various research applications, particularly in gastrointestinal studies and neuropharmacology, to explore the therapeutic potential of modulating CCK pathways.

    25 mg
    $1,275.00
    All 1 sizes
  • PD-135666
    Cat. No.
    A59708

    PD-135666

    PD-135666 is a potent dipeptide inhibitor of cholecystokinin B (CCK B) receptors, demonstrating an IC50 of 0.1 nM in mouse cerebral cortex. Unlike its enantiomer, PD-140548, which selectively targets CCK A receptors in rat pancreas, PD-135666 primarily interacts with CCK B receptors. This compound has been shown to exhibit anxiolytic effects in various animal models, making it a valuable tool for studying anxiety-related disorders and CCK receptor biology.

    25 mg
    $1,405.00
    50 mg
    $1,790.00
    All 3 sizes
  • Cholecystokinin-33 (swine)
    Cat. No.
    A59709

    Cholecystokinin-33 (swine)

    Cholecystokinin-33 (swine) is a biologically active fragment of cholecystokinin (CCK) that primarily targets CCK receptors. It is known to reduce food intake and promote gallbladder contraction, making it relevant for studies focused on appetite regulation and gastrointestinal motility. This peptide can be utilized in research to investigate its roles in digestive processes and related metabolic disorders.

    Out of stock

    All 3 sizes
  • (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
  • JMV 170
    Cat. No.
    A59711

    JMV 170

    JMV 170 is a selective CCK-B agonist that specifically targets the CCK-B receptor with a binding affinity ten times greater than that for the CCK-A receptor. This compound induces contractile effects in pig smooth muscle cells, exhibiting an EC50 value of 9 pmol/L. JMV 170 is primarily utilized in research applications focusing on gastrointestinal physiology and neurobiology, particularly in studies investigating the roles of cholecystokinin in smooth muscle contractility.

    Out of stock

    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
  • PD-149164
    Cat. No.
    A59717

    PD-149164

    PD-149164 is a selective agonist of the cholecystokinin B (CCK-B) receptor, exhibiting high binding affinity with IC50 values of 0.083 nM for CCK-B and 75 nM for CCK-A. This compound is instrumental in studying the role of CCK-B receptors in physiological and pathological processes, including appetite regulation, anxiety, and enhanced memory function. It serves as a valuable tool for research in neuropharmacology and gastrointestinal studies.

    Out of stock

    All 3 sizes
  • A-70874
    Cat. No.
    A59718

    A-70874

    A-70874 is a tyrosine-free tetrapeptide analog of cholecystokinin (CCK-4), acting as an agonist for pancreatic amylase release. It also serves as a partial agonist, promoting phosphoinositide decomposition in pancreatic cells. With an IC50 of 4.9 nM for the guinea pig pancreatic CCK receptor, A-70874 shows a notable affinity of 1.6 μM for the CCK-B/gastrin receptor. This compound is valuable for investigating the physiological roles of CCK receptors in both the digestive system and the central nervous system.

    25 mg
    $1,275.00
    All 1 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
  • CCK-A receptor inhibitor 1
    Cat. No.
    A59727

    CCK-A receptor inhibitor 1

    CCK-A receptor inhibitor 1 is a selective inhibitor of the cholecystokinin A (CCK-A) receptor, exhibiting a binding IC50 of 340 nM. By modulating CCK-A receptor activity, this compound plays a crucial role in studying gastrointestinal physiology and related disorders. Its inhibitory properties make it useful for research applications focused on appetite regulation and the gastrointestinal system.

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

Items 76-100 of 105

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