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  3. Eptifibatide

Eptifibatide is a cyclic heptapeptide, acts as a competitive antagonist for the activated platelet glycoprotein IIb/IIIa receptor, with anti-platelet activity.

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

Custom Peptide Synthesis

CAS No. : 188627-80-7

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Customer Review

Based on 9 publication(s) in Google Scholar

Other Forms of Eptifibatide:

Top Publications Citing Use of Products

    Eptifibatide purchased from MedChemExpress. Usage Cited in: Nat Commun. 2024 Apr 11;15(1):3129.  [Abstract]

    The median fluorescence intensity of HRG and platelets were calculated and plotted over time from mice treated or untreated with Eptifibatide (10 μg/g body weight, repeated every 15-20 min).

    Eptifibatide purchased from MedChemExpress. Usage Cited in: Nat Commun. 2024 Apr 11;15(1):3129.  [Abstract]

    The scatter plot of pixel intensities of green (HRG) and red (CD31) fluorescence in ROI1 and ROI2 as indicated were presented. The Pearson's correlation coefficients (r) for pixels with intensity above the threshold (indicated by the dashed lines) in the thrombus (ROI2) and in the area without the thrombus (ROI1-ROI2) were inserted. Veh vehicle, Epti eptifibatide.

    Eptifibatide purchased from MedChemExpress. Usage Cited in: Nat Commun. 2024 Apr 11;15(1):3129.  [Abstract]

    When mice were treated with eptifibatide, an integrin αIIbβ3 antagonist that eliminated platelet deposition and thus platelet-derived Zn2+, HRG accumulation at the site of vessel injury was significantly reduced by 58.3%.

    Eptifibatide purchased from MedChemExpress. Usage Cited in: Ghent University. 2018 May.

    Concentration eptifibatide in function of buffer volume eluted from the column.

    Eptifibatide purchased from MedChemExpress. Usage Cited in: Ghent University. 2018 May.

    Calibration curve eptifibatide (0.25 mg/mL-0,00012207 mg/mL).
    • Biological Activity

    • Purity & Documentation

    • References

    • Customer Review

    Description

    Eptifibatide is a cyclic heptapeptide, acts as a competitive antagonist for the activated platelet glycoprotein IIb/IIIa receptor, with anti-platelet activity[1].

    Cellular Effect
    Cell Line Type Value Description References
    Platelet IC50
    0.012 μM
    Compound: Eptifibatide
    Antiplatelet activity in platelet (unknown origin) assessed as inhibition of platelet aggregation
    Antiplatelet activity in platelet (unknown origin) assessed as inhibition of platelet aggregation
    [PMID: 24461295]
    In Vitro

    Eptifibatide is a cyclic heptapeptide, acts as a competitive antagonist for the activated platelet glycoprotein IIb/IIIa receptor, with anti-platelet activity[1].

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

    Clinical Trial
    Molecular Weight

    831.96

    Formula

    C35H49N11O9S2

    CAS No.
    Appearance

    Solid

    Color

    White to off-white

    Sequence

    MPA-HAR-Gly-Asp-Trp-Pro-Cys-NH2

    Sequence Shortening

    MPA-HAR-GDWPC-NH2

    Shipping

    Room temperature in continental US; may vary elsewhere.

    Storage

    Sealed storage, away from moisture and light

    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)

    Solvent & Solubility
    In Vitro: 

    DMSO : 200 mg/mL (240.40 mM; Need ultrasonic; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)

    H2O : 50 mg/mL (60.10 mM; Need ultrasonic)

    Preparing
    Stock Solutions
    Concentration Solvent Mass 1 mg 5 mg 10 mg
    1 mM 1.2020 mL 6.0099 mL 12.0198 mL
    5 mM 0.2404 mL 1.2020 mL 2.4040 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). 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
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    Concentration
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    Volume
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    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    40% PEG300    5% Tween-80    45% Saline

      Solubility: ≥ 2.08 mg/mL (2.50 mM); Clear solution

      This protocol yields a clear solution of ≥ 2.08 mg/mL (saturation unknown).

      Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (20.8 mg/mL) to 400 μL PEG300, and mix evenly; then add 50 μL Tween-80 and mix evenly; then add 450 μL Saline to adjust the volume to 1 mL.

      Preparation of Saline: Dissolve 0.9 g sodium chloride in ddH₂O and dilute to 100 mL to obtain a clear Saline solution.
    • Protocol 2

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

      Solubility: ≥ 2.08 mg/mL (2.50 mM); Clear solution

      This protocol yields a clear solution of ≥ 2.08 mg/mL (saturation unknown).

      Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (20.8 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.

    For the following dissolution methods, please prepare the working solution directly. It is recommended to prepare fresh solutions and use them promptly within a short period of time.
    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:  PBS

      Solubility: 100 mg/mL (120.20 mM); Clear solution; Need ultrasonic

    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

    Purity: 99.79%

    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). 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
    H2O / DMSO 1 mM 1.2020 mL 6.0099 mL 12.0198 mL 30.0495 mL
    5 mM 0.2404 mL 1.2020 mL 2.4040 mL 6.0099 mL
    10 mM 0.1202 mL 0.6010 mL 1.2020 mL 3.0050 mL
    15 mM 0.0801 mL 0.4007 mL 0.8013 mL 2.0033 mL
    20 mM 0.0601 mL 0.3005 mL 0.6010 mL 1.5025 mL
    25 mM 0.0481 mL 0.2404 mL 0.4808 mL 1.2020 mL
    30 mM 0.0401 mL 0.2003 mL 0.4007 mL 1.0017 mL
    40 mM 0.0300 mL 0.1502 mL 0.3005 mL 0.7512 mL
    50 mM 0.0240 mL 0.1202 mL 0.2404 mL 0.6010 mL
    60 mM 0.0200 mL 0.1002 mL 0.2003 mL 0.5008 mL
    DMSO 80 mM 0.0150 mL 0.0751 mL 0.1502 mL 0.3756 mL
    100 mM 0.0120 mL 0.0601 mL 0.1202 mL 0.3005 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.

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    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.

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    Product Name:
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    Cat. No.:
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