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 26-50 of 63

  • GV150013X
    Cat. No.
    A59663

    GV150013X

    GV150013X is a potent antagonist of the cholecystokinin-2/gastrin receptor (CCK2R), exhibiting a Ki value of 2.29 nM. This compound has demonstrated efficacy in attenuating central nervous system disorders, particularly in models of anxiety and panic disorder. Its application in research may provide valuable insights into the therapeutic potential for CCK2R modulation in neuropsychiatric conditions.

    1 mg
    $65.00
    5 mg
    $165.00
    All 7 sizes
  • RP 72540
    Cat. No.
    A59664

    RP 72540

    Synonyms: RPR101048

    RP 72540 is a selective antagonist of the CCK-B receptor, exhibiting IC50 values of 2.4 nM, 1.2 nM, and 3.8 nM in guinea pig, rat, and mouse cerebral cortices, respectively. This compound effectively inhibits CCK-8-induced neuronal firing and demonstrates a dose-dependent reduction in gastric acid secretion. RP 72540 serves as a valuable tool in research applications aiming to elucidate the physiological roles of CCK-B receptors, particularly in the context of gastrointestinal processes and neurophysiology.

    25 mg
    $1,275.00
    50 mg
    $1,625.00
    All 3 sizes
  • CI-1015
    Cat. No.
    A59667

    CI-1015

    Synonyms: PD 144598

    CI-1015 is a potent antagonist of the cholecystokinin B (CCK-B) receptor, which plays a critical role in gastrointestinal physiology and neurotransmission. This compound effectively inhibits CCK-B receptor activity, making it valuable for research into gastrointestinal disorders, anxiety, and pain modulation. Its specificity for the CCK-B receptor allows for the exploration of therapeutic avenues in conditions where CCK signaling is implicated.

    25 mg
    $1,275.00
    50 mg
    $1,625.00
    All 3 sizes
  • CI-988 meglumin
    Cat. No.
    A59671

    CI-988 meglumin

    Synonyms: PD134308 meglumin

    CI-988 meglumin is a potent cholecystokinin 2 receptor (CCK2R) antagonist. By inhibiting CCK2R, CI-988 meglumin plays a critical role in mitigating the gastrin-mediated cardioprotective effects associated with ischemia/reperfusion injury. This compound is valuable for research in cardiac physiology and pathophysiology, particularly in studies exploring receptor signaling and myocardial stress responses.

    Out of stock

    All 3 sizes
  • Gastrazole free acid
    Cat. No.
    A59676

    Gastrazole free acid

    Synonyms: JB95008 free acid

    Gastrazole free acid is a cholecystokinin receptor antagonist that demonstrates potential in inhibiting pancreatic cancer growth. By targeting gastrin receptors, this compound plays a crucial role in the modulation of gastric functions and may aid in the investigation of therapeutic strategies for gastrointestinal malignancies. Its utility in research provides insights into receptor-mediated pathways and cancer biology.

    25 mg
    $1,275.00
    50 mg
    $1,625.00
    All 3 sizes
  • PD 136450
    Cat. No.
    A59677

    PD 136450

    Synonyms: CAM 1189

    PD 136450 is a potent antagonist of cholecystokinin 2 (CCK2) receptors. This compound demonstrates significant biological activity, including anti-secretory, anxiolytic, and anti-ulcer effects. PD 136450 effectively inhibits gastric acid secretion with an IC50 of 1 mg/kg and significantly reduces hemorrhagic lesions in rat models, with an IC50 of 4.7 mg/kg. It is a valuable tool for investigating gastrointestinal disorders and evaluating potential therapeutic approaches in related pharmacological research.

    Out of stock

    All 3 sizes
  • Proglumide hemicalcium
    Cat. No.
    A59679

    Proglumide hemicalcium

    Proglumide hemicalcium is a non-peptide antagonist of cholecystokinin (CCK)-A/B receptors. It selectively inhibits the actions of CCK in the central nervous system, demonstrating key biological activities such as the inhibition of gastric secretion and protection of the gastroduodenal mucosa. Additionally, Proglumide hemicalcium exhibits antiepileptic and antioxidant properties, making it a valuable reagent for research in gastrointestinal protection and neurological studies.

    Out of stock

    All 3 sizes
  • JNJ-17156516
    Cat. No.
    A59681

    JNJ-17156516

    JNJ-17156516 is a potent and selective antagonist of the cholecystokinin (CCK)1 receptor. This compound demonstrates significant biological activity in inhibiting CCK-induced signaling, making it valuable for research in gastrointestinal physiology and related disorders. Its oral bioavailability positions it as a useful tool in the exploration of CCK1 receptor functions and therapeutic applications.

    25 mg
    $1,275.00
    50 mg
    $1,625.00
    All 3 sizes
  • Spiroglumide
    Cat. No.
    A59682

    Spiroglumide

    Synonyms: CR-2194

    Spiroglumide is a selective cholecystokinin B (CCKB) receptor antagonist. It demonstrates significant biological activity through the inhibition of CCKB receptor signaling, making it valuable for studying the physiological roles of cholecystokinin in various biological systems. Research applications include the investigation of gastrointestinal disorders and the exploration of potential therapeutic strategies in conditions linked with dysregulated CCKB receptor activity.

    1 mg
    $55.00
    5 mg
    $135.00
    All 7 sizes
  • PD 135158
    Cat. No.
    A59685

    PD 135158

    Synonyms: CAM 1028

    PD 135158 is a selective antagonist of the CCKB receptor, exhibiting an IC50 of 2.8 nM in mouse cortex assays. This compound demonstrates notable anxiolytic properties, making it a valuable tool for research into anxiety disorders and related neuropharmacological studies. Its specificity and potency make PD 135158 suitable for investigating the role of CCKB receptors in various biological contexts.

    25 mg
    $2,035.00
    50 mg
    $2,610.00
    All 3 sizes
  • LY262691
    Cat. No.
    A59686

    LY262691

    LY262691 is a selective antagonist of the cholecystokinin B (CCK-B) receptor, known for its antipsychotic properties. This compound effectively reduces the activity of spontaneously firing A9 and A10 dopamine neurons, making it a valuable tool in antipsychotic research. Its mechanism offers insights into the modulation of dopaminergic signaling pathways related to psychiatric disorders.

    25 mg
    $1,275.00
    50 mg
    $1,625.00
    All 3 sizes
  • LY 202769
    Cat. No.
    A59687

    LY 202769

    LY 202769 is a cholecystokinin (CCK) and gastrin receptor antagonist, providing a valuable tool for investigating the roles of these receptors in physiological processes. This compound exhibits potent antagonistic activity, making it suitable for research into gastrointestinal disorders as well as central nervous system diseases. Its application can aid in understanding the mechanisms of action associated with CCK and gastrin receptors in these pathologies.

    25 mg
    $1,275.00
    50 mg
    $1,625.00
    All 3 sizes
  • Lorglumide
    Cat. No.
    A59688

    Lorglumide

    Synonyms: CR-1409

    Lorglumide is a potent cholecystokinin (CCK) receptor antagonist that effectively blocks the activity of CCK at its receptors. This compound is instrumental in studying the regulation of pancreatic secretion and growth. Lorglumide serves as a valuable tool for investigating gastrointestinal physiology and related disorders.

    Out of stock

    All 3 sizes
  • Cholecystokinin (27-32)-amide
    Cat. No.
    A59689

    Cholecystokinin (27-32)-amide

    Synonyms: CCK-27-32-NH2

    Cholecystokinin (27-32)-amide is a potent antagonist of the cholecystokinin (CCK) receptor, primarily interfering with CCK-mediated signaling pathways. This compound exhibits significant biological activity in regulating digestive processes and satiety. It is widely utilized in research applications focused on gastrointestinal function, neuropeptide signaling, and potential therapeutic interventions for related disorders.

    Out of stock

    All 3 sizes
  • RP-69758
    Cat. No.
    A59690

    RP-69758

    RP-69758 is a selective non-peptide antagonist of the cholecystokinin-B (CCKB)/gastrin receptor, demonstrating over 200-fold specificity for CCKB compared to CCKA receptors. This compound effectively inhibits CCK-8-induced neuronal firing in rat hippocampal slices and suppresses pentagastrin-induced gastric acid secretion in rats. RP-69758 serves as a valuable tool for investigating neurological disorders and gastrointestinal diseases in research applications.

    Out of stock

    All 3 sizes
  • CHEMBL333994
    Cat. No.
    A59693

    CHEMBL333994

    Synonyms: FK-480

    CHEMBL333994 is a selective antagonist of the Cholecystokinin A receptor (CCK-A receptor), exhibiting a potent inhibitory activity with an IC50 of 0.67 nM. This compound selectively targets peripheral CCK receptors and has been shown to increase CCK mRNA levels. CHEMBL333994 is useful in research related to chronic pancreatitis, providing insights into its therapeutic potential in gastrointestinal disorders.

    1 mg
    $235.00
    5 mg
    $590.00
    All 6 sizes
  • GV-150013
    Cat. No.
    A59694

    GV-150013

    GV-150013 is a selective antagonist of the cholecystokinin B (CCK-B) receptor, known for its ability to modulate neurotransmitter activity. This compound is primarily utilized in studies investigating sleep regulation and related disorders. Its distinct mechanism of action positions GV-150013 as a valuable tool for research into the pharmacological management of sleep disturbances and anxiety-related conditions.

    1 mg
    $160.00
    5 mg
    $395.00
    All 7 sizes
  • JMV 167
    Cat. No.
    A59695

    JMV 167

    JMV 167 is a potent antagonist of the peripheral cholecystokinin receptor (CKK), exhibiting an IC50 value of 500 nM. This compound is valuable for research applications involving the modulation of digestive processes and appetite regulation. Its role in studying the effects of cholecystokinin signaling makes it an essential tool for investigating therapeutic strategies related to gastrointestinal disorders and metabolic conditions.

    25 mg
    $1,275.00
    All 1 sizes
  • L-740093
    Cat. No.
    A59697

    L-740093

    L-740093 is a potent cholecystokinin-B (CCK-B) receptor antagonist with significant central nervous system (CNS) penetration. This compound is utilized in research to investigate the role of CCK-B receptors in various physiological and pathological processes, including anxiety and pain modulation. Its ability to effectively cross the blood-brain barrier makes it a valuable tool for exploring CNS-related mechanisms.

    25 mg
    $1,275.00
    50 mg
    $1,625.00
    All 3 sizes
  • Benzotript
    Cat. No.
    A59698

    Benzotript

    Synonyms: Benzotriptum

    Benzotript is a cholecystokinin (CCK) and gastrin receptor antagonist. It exhibits significant antiproliferative effects in human colon carcinoma cell lines, making it valuable for cancer research. This compound can be employed in studies investigating the role of CCK and gastrin signaling pathways in tumor growth and development.

    1 mg
    $105.00
    2 mg
    $160.00
    All 7 sizes
  • L 368935
    Cat. No.
    A59699

    L 368935

    L 368935 is a potent antagonist of the cholecystokinin B receptor (CCKB receptor), demonstrating effective brain penetration and central activity. This compound is significant for research applications focused on neuropharmacology and gastrointestinal physiology, as well as studying the roles of CCKB receptors in various neurological disorders.

    25 mg
    $1,275.00
    50 mg
    $1,625.00
    All 3 sizes
  • 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
  • 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

Items 26-50 of 63

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