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  3. Isochlorogenic acid A

Isochlorogenic acid A  (Synonyms: 3,5-Dicaffeoylquinic acid; 3,5-CQA)

Cat. No.: HY-N0056 Purity: 99.53%
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Isochlorogenic acid A (3,5-Dicaffeoylquinic acid) is a natural phenolic acid with anti-mutagenicity, anti-HBV, anti-HIV, anti-oxidant, anti-bacterial, and anti-inflammatoryy activities.

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

CAS No. : 2450-53-5

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Solid + Solvent (Highly Recommended)
10 mM * 1 mL in DMSO
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Customer Review

Based on 13 publication(s) in Google Scholar

Other Forms of Isochlorogenic acid A:

Top Publications Citing Use of Products

    Isochlorogenic acid A purchased from MedChemExpress. Usage Cited in: Antiviral Res. 2025 Dec 4:245:106323.  [Abstract]

    Cytotoxicity assay of Isochlorogenic acid A (ICAA) on HepAD38 and HepG2 cells. Cells were incubated with different concentrations (up to 1000 μM) of ICAA for 6 days, and the toxicity was assessed using a cell viability assay (Presto Blue).

    Isochlorogenic acid A purchased from MedChemExpress. Usage Cited in: Antiviral Res. 2025 Dec 4:245:106323.  [Abstract]

    Isochlorogenic acid A (ICAA: 200 μM). Representative images from Western blots showing the intracellular core protein and its quantification.

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    • Biological Activity

    • Purity & Documentation

    • References

    • Customer Review

    Description

    Isochlorogenic acid A (3,5-Dicaffeoylquinic acid) is a natural phenolic acid with anti-mutagenicity, anti-HBV, anti-HIV, anti-oxidant, anti-bacterial, and anti-inflammatoryy activities[1].

    Cellular Effect
    Cell Line Type Value Description References
    HeLa IC50
    >500 μM
    Compound: RLE30
    Inhibition of HDAC in human HeLa cells using Boc-Lys(AC)-AMC as substrate after 24 to 48 hrs by spectrofluorometry
    Inhibition of HDAC in human HeLa cells using Boc-Lys(AC)-AMC as substrate after 24 to 48 hrs by spectrofluorometry
    [PMID: 26996372]
    HT-22 EC50
    >100 μM
    Compound: 25
    Neuroprotective activity against glutamate-induced cell death in mouse HT-22 cells assessed as increase in cell viability after 24 hrs by EZ-Cytox assay
    Neuroprotective activity against glutamate-induced cell death in mouse HT-22 cells assessed as increase in cell viability after 24 hrs by EZ-Cytox assay
    [PMID: 32991171]
    MT2 ED50
    1 μg/mL
    Compound: 3,5-DCQA
    Antiviral activity against HIV1 LAI in human MT2 cells assessed as virus-induced cytopathic effect after 72 hrs
    Antiviral activity against HIV1 LAI in human MT2 cells assessed as virus-induced cytopathic effect after 72 hrs
    [PMID: 11430019]
    MT2 ED50
    1.9 μM
    Compound: 3,5-dicaffeoylquinic acid
    Antiviral activity against HIV1 LAI in MT2 cells assessed as inhibition of virus-induced cytopathic effect
    Antiviral activity against HIV1 LAI in MT2 cells assessed as inhibition of virus-induced cytopathic effect
    [PMID: 18674899]
    MT2 ED50
    2 μM
    Compound: 3,5-DCQA
    Concentration that inhibits Human Immunodeficiency Virus Type 1 (HIV-1)-induced death of MT-2 cells
    Concentration that inhibits Human Immunodeficiency Virus Type 1 (HIV-1)-induced death of MT-2 cells
    [PMID: 9986720]
    MT2 IC50
    1.9 μM
    Compound: 8
    Inhibition of HIV1 integrase activity assessed as suppression of viral replication in human MT2 cells
    Inhibition of HIV1 integrase activity assessed as suppression of viral replication in human MT2 cells
    [PMID: 27676157]
    In Vitro

    Isochlorogenic acid A inhibits the aminoacylation activity of LeuRS from Giardia lamblia (GlLeuRS), with an IC50 of 5.82 μg/mL[1].
    Isochlorogenic acid A (5-100 μM, 48 h) increases melanin content in B16 cells, and increases TYR proteins activity[4].
    Isochlorogenic acid A shows DPPH (IC50=4.26 µg/mL), ABTS radical scavenging activity[6].
    Isochlorogenic acid A (0-250 μg/mL, 24 h) inhibits nitric oxide production in LPS-stimulated RAW 264.7 cells[6].

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

    Western Blot Analysis[4]

    Cell Line: B16 cells
    Concentration: 48 h
    Incubation Time: 5, 50, and 100 μM
    Result: Increased tyrosinase (TYR), TRP1, TRP2, p-MITF, and total MITF protein expressions.
    Induced the phosphorylation of Akt at Thr308.
    In Vivo

    Isochlorogenic acid A (5 and 10 mg/kg, p.o., once a day for 3 weeks) ameliorates cognitive impairment induced by TMT in ICR male mice[5].

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

    Animal Model: TMT-induced ICR male mice[5]
    Dosage: 5 and 10 mg/kg
    Administration: p.o., once a day for 3 weeks
    Result: Improved spatial memory and learning ability of mice in MWM test.
    Reduced the TMT-induced increased AChE activity.
    Reduced the MDA content compared to the TMT group.
    Molecular Weight

    516.45

    Formula

    C25H24O12

    CAS No.
    Appearance

    Solid

    Color

    White to light yellow

    SMILES

    OC(C=C1/C=C/C(O[C@H]2[C@@H]([C@@H](C[C@](O)(C2)C(O)=O)OC(/C=C/C3=CC(O)=C(C=C3)O)=O)O)=O)=C(C=C1)O

    Structure Classification
    Initial Source
    Shipping

    Room temperature in continental US; may vary elsewhere.

    Storage
    Powder -20°C 3 years
    4°C 2 years
    In solvent -80°C 6 months
    -20°C 1 month
    Solvent & Solubility
    In Vitro: 

    DMSO : ≥ 50 mg/mL (96.81 mM; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)

    *"≥" means soluble, but saturation unknown.

    Preparing
    Stock Solutions
    Concentration Solvent Mass 1 mg 5 mg 10 mg
    1 mM 1.9363 mL 9.6815 mL 19.3630 mL
    5 mM 0.3873 mL 1.9363 mL 3.8726 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. When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.

    • Molarity Calculator

    • Dilution Calculator

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

    Mass
    =
    Concentration
    ×
    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

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    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: ≥ 2.5 mg/mL (4.84 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 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: ≥ 2.5 mg/mL (4.84 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.
    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.
    Please enter your animal formula composition:
    %
    DMSO +
    +
    %
    Tween-80 +
    %
    Saline
    Recommended: Keep the proportion of DMSO in working solution below 2% if your animal is weak.
    The co-solvents required include: DMSO, . All of co-solvents are available by MedChemExpress (MCE). , Tween 80. All of co-solvents are available by MedChemExpress (MCE).
    Calculation results:
    Working solution concentration: mg/mL
    Method for preparing stock solution: mg drug dissolved in μL  DMSO (Stock solution concentration: mg/mL).
    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).
    Method for preparing in vivo working solution for animal experiments: Take μL DMSO stock solution, add μL . μL , mix evenly, next add μL Tween 80, mix evenly, then add μL Saline.
     If the continuous dosing period exceeds half a month, please choose this protocol carefully.
    Please ensure that the stock solution in the first step is dissolved to a clear state, and add co-solvents in sequence. You can use ultrasonic heating (ultrasonic cleaner, recommended frequency 20-40 kHz), vortexing, etc. to assist dissolution.
    Purity & Documentation

    Purity: 99.53%

    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. 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 1 mM 1.9363 mL 9.6815 mL 19.3630 mL 48.4074 mL
    5 mM 0.3873 mL 1.9363 mL 3.8726 mL 9.6815 mL
    10 mM 0.1936 mL 0.9681 mL 1.9363 mL 4.8407 mL
    15 mM 0.1291 mL 0.6454 mL 1.2909 mL 3.2272 mL
    20 mM 0.0968 mL 0.4841 mL 0.9681 mL 2.4204 mL
    25 mM 0.0775 mL 0.3873 mL 0.7745 mL 1.9363 mL
    30 mM 0.0645 mL 0.3227 mL 0.6454 mL 1.6136 mL
    40 mM 0.0484 mL 0.2420 mL 0.4841 mL 1.2102 mL
    50 mM 0.0387 mL 0.1936 mL 0.3873 mL 0.9681 mL
    60 mM 0.0323 mL 0.1614 mL 0.3227 mL 0.8068 mL
    80 mM 0.0242 mL 0.1210 mL 0.2420 mL 0.6051 mL
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    • 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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