1. Metabolic Enzyme/Protease
  2. Endogenous Metabolite
  3. Protocatechuic acid

Protocatechuic acid  (Synonyms: 3,4-Dihydroxybenzoic acid)

Cat. No.: HY-N0294 Purity: 99.98%
Handling Instructions Technical Support

Protocatechuic acid is a phenolic compound which exhibits neuroprotective effect.

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

CAS No. : 99-50-3

Size Price Stock Quantity
Free Sample (0.1 - 0.2 mg)   Apply Now  
Solid + Solvent (Highly Recommended)
10 mM * 1 mL in DMSO
ready for reconstitution
In-stock
Solution
10 mM * 1 mL in DMSO In-stock
Solid
200 mg In-stock
1 g In-stock
5 g   Get quote  
10 g   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 9 publication(s) in Google Scholar

Other Forms of Protocatechuic acid:

Top Publications Citing Use of Products

    Protocatechuic acid purchased from MedChemExpress. Usage Cited in: Cell Biol Toxicol. 2024 Nov 26;40(1):104.  [Abstract]

    MHCC97-H cells were first pretreated with Protocatechuic acid (PCA) (10 μM) for 16 h, followed by treatment with ferroptosis inducers, erastin (10 μM) and sorafenib (5 μM) for 24 h. Cell viability was evaluated using CCK-8.

    Protocatechuic acid purchased from MedChemExpress. Usage Cited in: Cell Biol Toxicol. 2024 Nov 26;40(1):104.  [Abstract]

    MHCC97-H cells were first pretreated with Protocatechuic acid (PCA) (10 μM) for 16 h, followed by treatment with ferroptosis inducers, erastin (10 μM) and sorafenib (5 μM) for 24 h. The mRNA expression of PTGS2, a marker gene for ferroptosis, was quantified using qPCR.

    Protocatechuic acid purchased from MedChemExpress. Usage Cited in: Cell Biol Toxicol. 2024 Nov 26;40(1):104.  [Abstract]

    To evaluate the effect of Protocatechuic acid (PCA) on hepatic steatosis, MHCC97-H cells were first pretreated with PCA (10 μM) for 16 h, and subsequently exposed to palmitic acid (PA, 200 μM) for 24 h. The accumulation of lipid droplets was quantified using Nile Red staining.

    Protocatechuic acid purchased from MedChemExpress. Usage Cited in: Cell Biol Toxicol. 2024 Nov 26;40(1):104.  [Abstract]

    The Protocatechuic acid (PCA) (10 μM) preconditioning also effectively reduced the cellular ROS level, contributing to the protection of PA-mediated lipotoxicity.

    Protocatechuic acid purchased from MedChemExpress. Usage Cited in: Cell Biol Toxicol. 2024 Nov 26;40(1):104.  [Abstract]

    MHCC97-H cells were exposed to various concentrations of Protocatechuic acid (PCA) (10 μM) for 16 h, after which the cell samples were collected for western blot analysis to ascertain the impact of PCA on NRF2 activation.

    View All Endogenous Metabolite Isoform Specific Products:

    • Biological Activity

    • Protocol

    • Purity & Documentation

    • References

    • Customer Review

    Description

    Protocatechuic acid is a phenolic compound which exhibits neuroprotective effect.

    IC50 & Target

    Microbial Metabolite

     

    Cellular Effect
    Cell Line Type Value Description References
    A549 IC50
    > 50 μM
    Compound: 6, Catechol
    Cytotoxicity against human A549 cells after 48 hrs by MTT assay
    Cytotoxicity against human A549 cells after 48 hrs by MTT assay
    [PMID: 26276433]
    BMDC IC50
    > 50 μM
    Compound: 2
    Inhibition of LPS-induced IL-12 p40 production in wild-type C57BL/6 mouse BMDC pretreated with compound for 1 hr before LPS treatment measured 16 hrs by ELISA
    Inhibition of LPS-induced IL-12 p40 production in wild-type C57BL/6 mouse BMDC pretreated with compound for 1 hr before LPS treatment measured 16 hrs by ELISA
    [PMID: 25769817]
    BMDC IC50
    > 50 μM
    Compound: 2
    Inhibition of LPS-induced IL-6 production in wild-type C57BL/6 mouse BMDC pretreated with compound for 1 hr before LPS treatment measured 16 hrs by ELISA
    Inhibition of LPS-induced IL-6 production in wild-type C57BL/6 mouse BMDC pretreated with compound for 1 hr before LPS treatment measured 16 hrs by ELISA
    [PMID: 25769817]
    BMDC IC50
    > 50 μM
    Compound: 2
    Inhibition of LPS-induced TNF-alpha production in wild-type C57BL/6 mouse BMDC pretreated with compound for 1 hr before LPS treatment measured 16 hrs by ELISA
    Inhibition of LPS-induced TNF-alpha production in wild-type C57BL/6 mouse BMDC pretreated with compound for 1 hr before LPS treatment measured 16 hrs by ELISA
    [PMID: 25769817]
    BMDM IC50
    89 μM
    Compound: Protocatechuic acid
    Inhibition of M-CSF/RANKL-induced osteoclast differentiation in C57BL/6 mouse bone marrow macrophage assessed as reduction in multinucleated TRAP+ cells incubated for 6 days with fresh media replacement on day 3 and measured on day 6 by TRAP staining-based microscopic analysis
    Inhibition of M-CSF/RANKL-induced osteoclast differentiation in C57BL/6 mouse bone marrow macrophage assessed as reduction in multinucleated TRAP+ cells incubated for 6 days with fresh media replacement on day 3 and measured on day 6 by TRAP staining-based microscopic analysis
    [PMID: 31257875]
    BV-2 IC50
    > 100 μM
    Compound: 27
    Antineuroinflammatory activity in mouse BV2 cells assessed as inhibition of LPS-induced NO production after 24 hrs in presence of LPS by Griess reaction based assay
    Antineuroinflammatory activity in mouse BV2 cells assessed as inhibition of LPS-induced NO production after 24 hrs in presence of LPS by Griess reaction based assay
    [PMID: 28911817]
    HEK293 IC50
    > 15 mM
    Compound: 6
    Cytotoxicity against HEK293 cells harboring pendrin P123S mutant after 72 hrs by MTT assay
    Cytotoxicity against HEK293 cells harboring pendrin P123S mutant after 72 hrs by MTT assay
    [PMID: 28341401]
    HL-60 IC50
    > 50 μM
    Compound: 6, Catechol
    Cytotoxicity against human HL60 cells after 48 hrs by MTT assay
    Cytotoxicity against human HL60 cells after 48 hrs by MTT assay
    [PMID: 26276433]
    HT-22 EC50
    > 100 μM
    Compound: 35
    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]
    L02 IC50
    > 50 μM
    Compound: 6, Catechol
    Cytotoxicity against human HL7702 cells after 48 hrs by MTT assay
    Cytotoxicity against human HL7702 cells after 48 hrs by MTT assay
    [PMID: 26276433]
    SMMC-7721 IC50
    > 50 μM
    Compound: 6, Catechol
    Cytotoxicity against human SMMC7721 cells after 48 hrs by MTT assay
    Cytotoxicity against human SMMC7721 cells after 48 hrs by MTT assay
    [PMID: 26276433]
    SW480 IC50
    > 50 μM
    Compound: 6, Catechol
    Cytotoxicity against human SW480 cells after 48 hrs by MTT assay
    Cytotoxicity against human SW480 cells after 48 hrs by MTT assay
    [PMID: 26276433]
    In Vitro

    Protocatechuic acid inhibits the aggregation of Aβ and αS and destabilizes their preformed fibrils. Protocatechuic acid prevents the death of PC12 cells triggered by Aβ- and αS-induced toxicity[3].

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

    In Vivo

    Protocatechuic acid is able to prevent stress induced immobility time in forced swim test without altering locomotor activity in mice. Further, Protocatechuic acid treatment attenuates the elevation of serum corticosterone, lipid peroxidation and restores enzymatic antioxidants in cerebral cortex and hippocampus in ARS mice[1]. Rat administered cadmium and treated with prostigmine and doses of Protocatechuic acid (10 20 mg/kg) has significantly reduced BChE activity. Cadmium and either Prostigmine or Protocatechuic acid (10 20 mg/kg) treated rats shows significant reduction in MDA level[2].

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

    Clinical Trial
    Molecular Weight

    154.12

    Formula

    C7H6O4

    CAS No.
    Appearance

    Solid

    Color

    White to off-white

    SMILES

    O=C(O)C1=CC=C(O)C(O)=C1

    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 : 100 mg/mL (648.85 mM; Need ultrasonic; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)

    H2O : 10 mg/mL (64.88 mM; Need ultrasonic)

    Preparing
    Stock Solutions
    Concentration Solvent Mass 1 mg 5 mg 10 mg
    1 mM 6.4885 mL 32.4423 mL 64.8845 mL
    5 mM 1.2977 mL 6.4885 mL 12.9769 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.

    * 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    40% PEG300    5% Tween-80    45% Saline

      Solubility: ≥ 2.5 mg/mL (16.22 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 (16.22 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.

    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: 16.67 mg/mL (108.16 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.
    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: 99.98%

    References
    Kinase Assay
    [2]

    AChE activity investigation is carried out in a reaction mixture containing 50 μL of tissue homogenate, 50 μL of 5, 5'-dithiobis-(2-nitrobenzoic) acid (DTNB), 1175 μL of 0.1 M phosphate-buffered solution, pH 8.0. After incubation for 20 min at 25°C, 25 μL of acetylthiocholine iodide solution is added as the substrate. The AChE activity is determined as changes in absorbance reading at 412 nm for 3 min at 25°C and using a UV/Visible spectrophotometer.

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

    Cell Assay
    [3]

    Dilutions of Protocatechuic acid (2, 5, 10, 20, 50, and 100 μM) are prepared from stock solutions, with serum-free culture medium. Equal volumes of each solution are mixed with Aβ1-42 (10 μM), then incubated for 24 h on a thermoblock, with continuous agitation, and then exposed to PC12 cells for 24 h to test whether Protocatechuic acid can prevent cell death triggered by Aβ. Cell viability is determined by MTT reduction assay. Cells are treated with 200 μL per well of MTT solution (final concentration, 0.5 mg/mL in DMEM-Glutamax medium) for 3 h, at 37°C, with 5% CO2. The dark blue formazan crystals that formed are solubilized with 100 μL per well of DMSO, for 30 min. Absorbance is measured at 540 nm, with a microplate reader. Results are expressed as the percentage of MTT reduction in relation to the absorbance of control cells at 100%.

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

    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
    H2O / DMSO 1 mM 6.4885 mL 32.4423 mL 64.8845 mL 162.2113 mL
    5 mM 1.2977 mL 6.4885 mL 12.9769 mL 32.4423 mL
    10 mM 0.6488 mL 3.2442 mL 6.4885 mL 16.2211 mL
    15 mM 0.4326 mL 2.1628 mL 4.3256 mL 10.8141 mL
    20 mM 0.3244 mL 1.6221 mL 3.2442 mL 8.1106 mL
    25 mM 0.2595 mL 1.2977 mL 2.5954 mL 6.4885 mL
    30 mM 0.2163 mL 1.0814 mL 2.1628 mL 5.4070 mL
    40 mM 0.1622 mL 0.8111 mL 1.6221 mL 4.0553 mL
    50 mM 0.1298 mL 0.6488 mL 1.2977 mL 3.2442 mL
    60 mM 0.1081 mL 0.5407 mL 1.0814 mL 2.7035 mL
    DMSO 80 mM 0.0811 mL 0.4055 mL 0.8111 mL 2.0276 mL
    100 mM 0.0649 mL 0.3244 mL 0.6488 mL 1.6221 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:
    Protocatechuic acid
    Cat. No.:
    HY-N0294
    Quantity:
    MCE Japan Authorized Agent: