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Catalpol (Catalpinoside), an iridoid glycoside found in Rehmannia glutinosa. Catalpol has neuroprotective, hypoglycemic, anti-inflammatory, anti-cancer, anti-spasmodic, anti-oxidant effects and anti-HBV effects.

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

CAS No. : 2415-24-9

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10 mM * 1 mL in DMSO
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Customer Review

Based on 13 publication(s) in Google Scholar

Other Forms of Catalpol:

Top Publications Citing Use of Products

    Catalpol purchased from MedChemExpress. Usage Cited in: Bioeng Transl Med. 2024 Dec 29;10(3):e10746.

    Organoids (generation of cerebral organoids; 22 D; 10 uM). Immunofluorescence staining for TBR1 (red), SOX2 (green), and DAPI (blue) in day 30 control and Catalpol-treated organoids.

    Catalpol purchased from MedChemExpress. Usage Cited in: Sci Rep. 2024 Nov 16;14(1):28327.  [Abstract]

    Catalpol (HUVECs; 1, 10, 100 µM; for 24 h). Western blots were conducted to detect the Bax, Bcl2, Cyto C, C-casp3 expression level. β-Actin was used as the endogenous control.

    Catalpol purchased from MedChemExpress. Usage Cited in: J Ethnopharmacol. 2024 May 6:331:118272.  [Abstract]

    Bar charts showing the length of the regenerating fin of zebrafish exposure to different concentrations of Catalpol (2 days) at 2 dpa, n = 8~20. The results indicated that 0.5 mg/L was the optimal concentration for Catalpol to exert its pro-regenerative effect.

    Catalpol purchased from MedChemExpress. Usage Cited in: Acta Pharmacol Sin. 2022 Jul;43(7):1670-1685.  [Abstract]

    The numbers of vessels and neurons in the cortex near the infarcted area were up-regulated in Catalpol (Rat; i.v, 2.5, 5.0, 10.0 mg/kg/d; for 14 d) groups.
    • Biological Activity

    • Purity & Documentation

    • References

    • Customer Review

    Description

    Catalpol (Catalpinoside), an iridoid glycoside found in Rehmannia glutinosa. Catalpol has neuroprotective, hypoglycemic, anti-inflammatory, anti-cancer, anti-spasmodic, anti-oxidant effects and anti-HBV effects[1][2][3].

    Cellular Effect
    Cell Line Type Value Description References
    A2780 GI50
    > 100 μM
    Compound: 1, catalpol
    Antiproliferative activity against human A2780 cells after 48 hrs by SRB assay
    Antiproliferative activity against human A2780 cells after 48 hrs by SRB assay
    [PMID: 17178223]
    A2780 GI50
    > 100 μM
    Compound: 2
    Antiproliferative activity against human A2780 cells after 48 hrs by sulforhodamine B assay
    Antiproliferative activity against human A2780 cells after 48 hrs by sulforhodamine B assay
    [PMID: 20231098]
    A2780 IC50
    > 10 μM
    Compound: 10
    Cytotoxicity against human A2780 cells by MTT assay
    Cytotoxicity against human A2780 cells by MTT assay
    [PMID: 26859776]
    A549 IC50
    > 10 μM
    Compound: 10
    Cytotoxicity against human A549 cells by MTT assay
    Cytotoxicity against human A549 cells by MTT assay
    [PMID: 26859776]
    BGC-823 IC50
    > 10 μM
    Compound: 10
    Cytotoxicity against human BGC823 cells by MTT assay
    Cytotoxicity against human BGC823 cells by MTT assay
    [PMID: 26859776]
    BV-2 IC50
    7.3 μM
    Compound: 10
    Inhibition of LPS-induced NO production in mouse BV2 cells assessed as reduction in nitrite level pretreated for 24 hrs before LPS treatment for additional 24 hrs by Griess reaction method
    Inhibition of LPS-induced NO production in mouse BV2 cells assessed as reduction in nitrite level pretreated for 24 hrs before LPS treatment for additional 24 hrs by Griess reaction method
    [PMID: 26859776]
    Bel-7402 IC50
    > 10 μM
    Compound: 10
    Cytotoxicity against human Bel7402 cells by MTT assay
    Cytotoxicity against human Bel7402 cells by MTT assay
    [PMID: 26859776]
    HBL-100 GI50
    > 100 μM
    Compound: 2
    Antiproliferative activity against human HBL100 cells after 48 hrs by sulforhodamine B assay
    Antiproliferative activity against human HBL100 cells after 48 hrs by sulforhodamine B assay
    [PMID: 20231098]
    HT-29 IC50
    > 10 μM
    Compound: 10
    Cytotoxicity against human HT-29 cells by MTT assay
    Cytotoxicity against human HT-29 cells by MTT assay
    [PMID: 26859776]
    HeLa GI50
    > 100 μM
    Compound: 2
    Antiproliferative activity against human HeLa cells after 48 hrs by sulforhodamine B assay
    Antiproliferative activity against human HeLa cells after 48 hrs by sulforhodamine B assay
    [PMID: 20231098]
    SW1573 GI50
    > 100 μM
    Compound: 1, catalpol
    Antiproliferative activity against human SW1573 cells after 48 hrs by SRB assay
    Antiproliferative activity against human SW1573 cells after 48 hrs by SRB assay
    [PMID: 17178223]
    SW1573 GI50
    > 100 μM
    Compound: 2
    Antiproliferative activity against human SW1573 cells after 48 hrs by sulforhodamine B assay
    Antiproliferative activity against human SW1573 cells after 48 hrs by sulforhodamine B assay
    [PMID: 20231098]
    T47D GI50
    > 100 μM
    Compound: 1, catalpol
    Antiproliferative activity against human T47D cells after 48 hrs by SRB assay
    Antiproliferative activity against human T47D cells after 48 hrs by SRB assay
    [PMID: 17178223]
    T47D GI50
    > 100 μM
    Compound: 2
    Antiproliferative activity against human T47D cells after 48 hrs by sulforhodamine B assay
    Antiproliferative activity against human T47D cells after 48 hrs by sulforhodamine B assay
    [PMID: 20231098]
    WiDr GI50
    > 100 μM
    Compound: 1, catalpol
    Antiproliferative activity against human WiDr cells after 48 hrs by SRB assay
    Antiproliferative activity against human WiDr cells after 48 hrs by SRB assay
    [PMID: 17178223]
    WiDr GI50
    > 100 μM
    Compound: 2
    Antiproliferative activity against human WiDr cells after 48 hrs by sulforhodamine B assay
    Antiproliferative activity against human WiDr cells after 48 hrs by sulforhodamine B assay
    [PMID: 20231098]
    In Vitro

    Catalpol (0.1 μg/mL; for 3 days) can induce neuronal differentiation in PC12 cells through activation of the intracellular signal transduction pathway, and promote neurite length[2].

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

    In Vivo

    Catalpol (25-100 mg/kg; intraperitoneal injection; once) treatment clearly reduces blood urea nitrogen, serum creatinine levels and the expression of KIM-1 in renal ischemia/reperfusion-injury (IRI) mice. Catalpol markedly reduces the expression of PI3K, Akt and eNOS levels, and suppresses the TNF-α, IL-1β, IL-6 and IL-10 activities[1].

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

    Animal Model: C57BL/6 mice treated with renal ischemia/reperfusion surgery[1]
    Dosage: 25 mg/kg, 50 mg/kg and 100 mg/kg
    Administration: Intraperitoneal injection; once
    Result: Clearly reduced blood urea nitrogen, serum creatinine levels and the expression of KIM-1 in renal IRI mice.
    Molecular Weight

    362.33

    Formula

    C15H22O10

    CAS No.
    Appearance

    Solid

    Color

    White to off-white

    SMILES

    OC[C@@]12[C@]([C@@H]3O[C@]([C@@H]([C@@H](O)[C@@H]4O)O)([H])O[C@@H]4CO)([H])[C@](C=CO3)([H])[C@H](O)[C@@H]1O2

    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 (275.99 mM; Need ultrasonic; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)

    H2O : 7.14 mg/mL (19.71 mM; ultrasonic and warming and heat to 60°C)

    Preparing
    Stock Solutions
    Concentration Solvent Mass 1 mg 5 mg 10 mg
    1 mM 2.7599 mL 13.7996 mL 27.5992 mL
    5 mM 0.5520 mL 2.7599 mL 5.5198 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: ≥ 2.08 mg/mL (5.74 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 (5.74 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.
    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: 99.86%

    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 2.7599 mL 13.7996 mL 27.5992 mL 68.9979 mL
    5 mM 0.5520 mL 2.7599 mL 5.5198 mL 13.7996 mL
    10 mM 0.2760 mL 1.3800 mL 2.7599 mL 6.8998 mL
    15 mM 0.1840 mL 0.9200 mL 1.8399 mL 4.5999 mL
    DMSO 20 mM 0.1380 mL 0.6900 mL 1.3800 mL 3.4499 mL
    25 mM 0.1104 mL 0.5520 mL 1.1040 mL 2.7599 mL
    30 mM 0.0920 mL 0.4600 mL 0.9200 mL 2.2999 mL
    40 mM 0.0690 mL 0.3450 mL 0.6900 mL 1.7249 mL
    50 mM 0.0552 mL 0.2760 mL 0.5520 mL 1.3800 mL
    60 mM 0.0460 mL 0.2300 mL 0.4600 mL 1.1500 mL
    80 mM 0.0345 mL 0.1725 mL 0.3450 mL 0.8625 mL
    100 mM 0.0276 mL 0.1380 mL 0.2760 mL 0.6900 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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      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:
    Catalpol
    Cat. No.:
    HY-N0820
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