1. GPCR/G Protein Neuronal Signaling Apoptosis PI3K/Akt/mTOR
  2. Cholecystokinin Receptor Apoptosis PI3K Akt
  3. Sincalide

Sincalide  (Synonyms: Cholecystokinin octapeptide; CCK-8; SQ19844)

Cat. No.: HY-P0093 Purity: 99.30%
Handling Instructions Technical Support

Sincalide (Cholecystokinin octapeptide, CCK-8) is a rapid-acting amino acid polypeptide hormone analogue of cholecystokinin (CCK) for intravenous use in postevacuation cholecystography. Sincalide is a major bioactive segment of CCK that retains most of the biological activities of CCK. Sincalide can promote gallbladder contraction by injection and helps diagnose gallbladder and pancreas disorders. Sincalide can increase bile secretion, cause the gallbladder to contract and relax the sphincter of Oddi, resulting in bile drainage into the duodenum. Sincalide is a major bioactive segment of CCK that retains most of the biological activities of CCK.

For research use only. We do not sell to patients.

Custom Peptide Synthesis

CAS No. : 25126-32-3

Size Price Stock Quantity
1 mg In-stock
5 mg In-stock
10 mg In-stock
50 mg   Get quote  
100 mg   Get quote  

* Please select Quantity before adding items.

This product is a controlled substance and not for sale in your territory.

Customer Review

Based on 4 publication(s) in Google Scholar

Other Forms of Sincalide:

Top Publications Citing Use of Products
Bio/Physico-chemical Assay
Cell Imaging/Staining
RT-PCR
Cell Proliferation/Viability Assay

    Sincalide purchased from MedChemExpress. Usage Cited in: J Gene Med. 2025 Dec;27(12):e70063.  [Abstract]

    Sincalide (Cholecystokinin; CCK) increased the expression of IL-6, TNF-α, and IL-1β in 266-6 cells.

    Sincalide purchased from MedChemExpress. Usage Cited in: Antioxidants (Basel). 2022 Dec 31;12(1):100.

    After transfection with GPX4 siRNA, mouse pancreatic acinar carcinoma 266-6 cells were treated with Sincalide (Cholecystokinin; CCK) (5 μM; 6 h), and lipid reactive oxygen species (ROS) levels and the extent of cell death were determined.

    Sincalide purchased from MedChemExpress. Usage Cited in: Immunogenetics. 2023 Feb;75(1):17-25.  [Abstract]

    Sincalide (CCK-8) (10 μL; 37 ℃; 2 h) was used to evaluate the proliferative ability of LUAD cells.

    Sincalide purchased from MedChemExpress. Usage Cited in: Immunogenetics. 2023 Feb;75(1):17-25.  [Abstract]

    Sincalide (CCK-8) (10 μL; 37 ℃; 2 h) was used to illustrate that si-IL4I1 + RO8191 had the ability to reverse the restraining impact of si-IL4I1 on LUAD cell proliferation.

    Sincalide purchased from MedChemExpress. Usage Cited in: Biomed Pharmacother. 2019 Aug:116:109001.  [Abstract]

    The OATP superfamily blocker Sincalide (SIN) (20 μM; 2 h) blocked Caba-780 uptake in renal cell carcinoma (RCC) cells.

    View All Cholecystokinin Receptor Isoform Specific Products:

    View All PI3K Isoform Specific Products:

    View All Akt Isoform Specific Products:

    • Biological Activity

    • Purity & Documentation

    • References

    • Customer Review

    Description

    Sincalide (Cholecystokinin octapeptide, CCK-8) is a rapid-acting amino acid polypeptide hormone analogue of cholecystokinin (CCK) for intravenous use in postevacuation cholecystography. Sincalide is a major bioactive segment of CCK that retains most of the biological activities of CCK. Sincalide can promote gallbladder contraction by injection and helps diagnose gallbladder and pancreas disorders. Sincalide can increase bile secretion, cause the gallbladder to contract and relax the sphincter of Oddi, resulting in bile drainage into the duodenum. Sincalide is a major bioactive segment of CCK that retains most of the biological activities of CCK[1][2][3].

    Cellular Effect
    Cell Line Type Value Description References
    CHO EC50
    0.63 nM
    Compound: CCK-8
    Affinity against Cholecystokinin type B receptor expressed in CHO cells on rat brain.
    Affinity against Cholecystokinin type B receptor expressed in CHO cells on rat brain.
    [PMID: 11020275]
    CHO EC50
    0.63 nM
    Compound: CCK8
    Effective concentration for the stimulation of Inositol Phosphate accumulation in CHO cells expressing wild-type Cholecystokinin type B receptor
    Effective concentration for the stimulation of Inositol Phosphate accumulation in CHO cells expressing wild-type Cholecystokinin type B receptor
    [PMID: 9057851]
    CHO IC50
    1.2 x 10-10 M
    Compound: CCK-8s
    Displacement of [125I]CCK-8s from human recombinant CCK-B receptor expressed in CHO cells
    Displacement of [125I]CCK-8s from human recombinant CCK-B receptor expressed in CHO cells
    [PMID: 26988801]
    CHO IC50
    1.2 x 10-10 M
    Compound: CCK-8s
    Displacement of [125I]CCK-8s from human recombinant CCK2 receptor expressed in CHO cells measured after 60 mins by scintillation counting method
    Displacement of [125I]CCK-8s from human recombinant CCK2 receptor expressed in CHO cells measured after 60 mins by scintillation counting method
    [PMID: 27876250]
    CHO IC50
    1.3 x 10-10 M
    Compound: CCK-8s
    Displacement of [125I]CCK-8s from human recombinant CCK-A receptor expressed in CHO cells
    Displacement of [125I]CCK-8s from human recombinant CCK-A receptor expressed in CHO cells
    [PMID: 26988801]
    CHO IC50
    1.3 x 10-10 M
    Compound: CCK-8s
    Displacement of [125I]CCK-8s from human recombinant CCK1 receptor expressed in CHO cells measured after 60 mins by scintillation counting method
    Displacement of [125I]CCK-8s from human recombinant CCK1 receptor expressed in CHO cells measured after 60 mins by scintillation counting method
    [PMID: 27876250]
    HEK293 EC50
    27 nM
    Compound: CCK-8, SO3
    Antagonist activity at CCK2 receptor expressed in HEK293 cells assessed as accumulation of [3H]inositol phosphates by PI assay
    Antagonist activity at CCK2 receptor expressed in HEK293 cells assessed as accumulation of [3H]inositol phosphates by PI assay
    [PMID: 16686530]
    HEK293 EC50
    28 nM
    Compound: CCK-8, SO3
    Antagonist activity at CCK1 receptor expressed in HEK 293 cells assessed as accumulation of [3H]inositol phosphates by PI assay
    Antagonist activity at CCK1 receptor expressed in HEK 293 cells assessed as accumulation of [3H]inositol phosphates by PI assay
    [PMID: 16686530]
    Jurkat EC50
    0.093 nM
    Compound: sincalide
    Displacement of [125I]CCK-8 from CCK2 receptor in human FGS7 Jurkat cells
    Displacement of [125I]CCK-8 from CCK2 receptor in human FGS7 Jurkat cells
    [PMID: 16562853]
    Jurkat EC50
    2 nM
    Compound: CCK-8S
    Compound was evaluated for calcium mobilization in Jurkat cells
    Compound was evaluated for calcium mobilization in Jurkat cells
    [PMID: 10866391]
    In Vitro

    Sincalide (Cholecystokinin octapeptide, CCK-8), as a novel cardiovascular hormone, has a significant inhibitory effect on myocardial fibrosis in noninfarcted areas. Sincalide also plays a positive role in fighting inflammation, apoptosis and collagen deposition. Sincalide protects H9c2 cardiomyoblasts from Ang II-induced apoptosis partly via activation of the CCK1 receptor and the phosphatidyqinositol-3 kinase/protein kinase B (PI3K/Akt) signaling pathway[3].

    MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

    Cell Viability Assay[3]

    Cell Line: H9c2 cells
    Concentration: 0.001, 0.01, 0.1, 1, 10, or 100 μmol/L
    Incubation Time: 24 h
    Result: Attenuated Ang II‐induced toxicity in H9c2 cells

    Apoptosis Analysis[3]

    Cell Line: H9c2 cells
    Concentration: 0.001, 0.01, 0.1, 1, 10, or 100 μmol/L
    Incubation Time: 24 h
    Result: Decreased apoptotic cells, and prevented Ang II‐induced cytotoxicity that involves modulation of the PI3K/Akt pathway.

    Western Blot Analysis[3]

    Cell Line: H9c2 cells
    Concentration: 0.001, 0.01, 0.1, 1, 10, or 100 μmol/L
    Incubation Time: 24 h
    Result: Expressed the protein and mRNAs of CCK and both its receptors in H9c2 cells.

    RT-PCR[3]

    Cell Line: H9c2 cells
    Concentration: 0.001, 0.01, 0.1, 1, 10, or 100 μmol/L
    Incubation Time: 24 h
    Result: Increased the protein and mRNA expression levels of CCK and decreased CCK 1 receptor expression levels at both the protein and mRNA levels with Ang II stimulation markedly.
    In Vivo

    Sincalide (Cholecystokinin octapeptide, CCK-8) (i.p.; 50 μg/kg/d; for 4 weeks) alleviates fibrosis in the noninfarcted regions and delay the left ventricular remodeling and the progress of heart failure in a MI rat model[4].

    MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

    Animal Model: MI rat model[4]
    Dosage: 50 μg/kg
    Administration: i.p.; 50 μg/kg/d; for 4 weeks
    Result: Had significant inhibitory effect on myocardial fibrosis in noninfarcted areas.
    Molecular Weight

    1143.27

    Formula

    C49H62N10O16S3

    CAS No.
    Appearance

    Solid

    Color

    White to off-white

    Sequence

    Asp-{SO3H-Tyr}-Met-Gly-Trp-Met-Asp-Phe-NH2

    Sequence Shortening

    D-{SO3H-Tyr}-MGWMDF-NH2

    Shipping

    Room temperature in continental US; may vary elsewhere.

    Storage

    Sealed storage, away from moisture and light, under nitrogen

    Powder -80°C 2 years
    -20°C 1 year

    *In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture and light, under nitrogen)

    Solvent & Solubility
    In Vitro: 

    H2O : 50 mg/mL (43.73 mM; ultrasonic and adjust pH to 11 with NH3·H2O)

    DMF : 50 mg/mL (43.73 mM; Need ultrasonic)

    DMSO : 25 mg/mL (21.87 mM; Need ultrasonic; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)

    Preparing
    Stock Solutions
    Concentration Solvent Mass 1 mg 5 mg 10 mg
    1 mM 0.8747 mL 4.3734 mL 8.7468 mL
    5 mM 0.1749 mL 0.8747 mL 1.7494 mL
    View the Complete Stock Solution Preparation Table

    * Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
    Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture and light, under nitrogen). When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.

    * Note: If you choose water as the stock solution, please dilute it to the working solution, then filter and sterilize it with a 0.22 μm filter before use.

    • Molarity Calculator

    • Dilution Calculator

    Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

    Mass
    =
    Concentration
    ×
    Volume
    ×
    Molecular Weight *

    Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

    This equation is commonly abbreviated as: C1V1 = C2V2

    Concentration (start)

    C1

    ×
    Volume (start)

    V1

    =
    Concentration (final)

    C2

    ×
    Volume (final)

    V2

    In Vivo:

    Select the appropriate dissolution method based on your experimental animal and administration route.

    For the following dissolution methods, please ensure to first prepare a clear stock solution using an In Vitro approach and then sequentially add co-solvents:
    To ensure reliable experimental results, the clarified stock solution can be appropriately stored based on storage conditions. As for the working solution for in vivo experiments, it is recommended to prepare freshly and use it on the same day.
    The percentages shown for the solvents indicate their volumetric ratio in the final prepared solution. If precipitation or phase separation occurs during preparation, heat and/or sonication can be used to aid dissolution.

    • Protocol 1

      Add each solvent one by one:  10% DMSO    90% (20% SBE-β-CD in Saline)

      Solubility: ≥ 2.5 mg/mL (2.19 mM); Clear solution

      This protocol yields a clear solution of ≥ 2.5 mg/mL (saturation unknown).

      Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (25.0 mg/mL) to 900 μL 20% SBE-β-CD in Saline, and mix evenly.

      Preparation of 20% SBE-β-CD in Saline (4°C, storage for one week): 2 g SBE-β-CD powder is dissolved in 10 mL Saline, completely dissolve until clear.
    • Protocol 2

      Add each solvent one by one:  10% DMSO    90% Corn Oil

      Solubility: ≥ 2.5 mg/mL (2.19 mM); Clear solution

      This protocol yields a clear solution of ≥ 2.5 mg/mL (saturation unknown). If the continuous dosing period exceeds half a month, please choose this protocol carefully.

      Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (25.0 mg/mL) to 900 μL Corn oil, and mix evenly.

    In Vivo Dissolution Calculator
    Please enter the basic information of animal experiments:

    Dosage

    mg/kg

    Animal weight
    (per animal)

    g

    Dosing volume
    (per animal)

    μL

    Number of animals

    Recommended: Prepare an additional quantity of animals to account for potential losses during experiments.
    Calculation results:
    Working solution concentration: mg/mL
    This product has good water solubility, please refer to the measured solubility data in water/PBS/Saline for details.
    The concentration of the stock solution you require exceeds the measured solubility. The following solution is for reference only.If necessary, please contact MedChemExpress (MCE).
    Purity & Documentation
    References

    Complete Stock Solution Preparation Table

    * Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
    Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture and light, under nitrogen). When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.

    Optional Solvent Concentration Solvent Mass 1 mg 5 mg 10 mg 25 mg
    DMSO / H2O / DMF 1 mM 0.8747 mL 4.3734 mL 8.7468 mL 21.8671 mL
    5 mM 0.1749 mL 0.8747 mL 1.7494 mL 4.3734 mL
    10 mM 0.0875 mL 0.4373 mL 0.8747 mL 2.1867 mL
    15 mM 0.0583 mL 0.2916 mL 0.5831 mL 1.4578 mL
    20 mM 0.0437 mL 0.2187 mL 0.4373 mL 1.0934 mL
    H2O / DMF 25 mM 0.0350 mL 0.1749 mL 0.3499 mL 0.8747 mL
    30 mM 0.0292 mL 0.1458 mL 0.2916 mL 0.7289 mL
    40 mM 0.0219 mL 0.1093 mL 0.2187 mL 0.5467 mL

    * Note: If you choose water as the stock solution, please dilute it to the working solution, then filter and sterilize it with a 0.22 μm filter before use.

    • No file chosen (Maximum size is: 1024 Kb)
    • If you have published this work, please enter the PubMed ID.
    • Your name will appear on the site.
    Help & FAQs
    • Do most proteins show cross-species activity?

      Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

    Your Recently Viewed Products:

    Inquiry Online

    Your information is safe with us. * Required Fields.

    Product Name

     

    Requested Quantity *

    Applicant Name *

     

    Salutation

    Email Address *

     

    Phone Number *

    Department

     

    Organization Name *

    City

    State

    Country or Region *

         

    Remarks

    Bulk Inquiry

    Inquiry Information

    Product Name:
    Sincalide
    Cat. No.:
    HY-P0093
    Quantity:
    MCE Japan Authorized Agent: