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Genkwanin is a major non-glycosylated flavonoid with anti-flammatory activities.

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

CAS No. : 437-64-9

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10 mM * 1 mL in DMSO
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Customer Review

Based on 9 publication(s) in Google Scholar

Other Forms of Genkwanin:

Top Publications Citing Use of Products

    Genkwanin purchased from MedChemExpress. Usage Cited in: Phytomedicine. 2025 Sep 24:148:157306.  [Abstract]

    HE staining analysis of pathological damage in the heart, liver, lung, and kidney tissues of mice treated with H-GKA (20 mg/kg, i.p.).

    Genkwanin purchased from MedChemExpress. Usage Cited in: Phytomedicine. 2025 Sep 24:148:157306.  [Abstract]

    DYRK1A expression in lung tissues of asthmatic mice and mice after GKA (5, 10, 20 mg/kg, i.p.) treatment was examined using immunoblotting.

    Genkwanin purchased from MedChemExpress. Usage Cited in: Phytomedicine. 2025 Sep 24:148:157306.  [Abstract]

    Detection of ROS in lung tissues of mice by DCFH-DA with GKA (5, 10, 20 mg/kg, i.p.) treatment.

    Genkwanin purchased from MedChemExpress. Usage Cited in: Phytomedicine. 2025 Sep 24:148:157306.  [Abstract]

    DYRK1A expression in lung tissues of asthmatic mice and mice after GKA (5, 10, 20 mg/kg, i.p.) treatment was examined using g dual-labeling immunofluorescence.

    Genkwanin purchased from MedChemExpress. Usage Cited in: Phytomedicine. 2025 Sep 24:148:157306.  [Abstract]

    The cell viability of BEAS-2B cells was examined using CCK-8 assays after GKA (30 μM) treatment.
    • Biological Activity

    • Purity & Documentation

    • References

    • Customer Review

    Description

    Genkwanin is a major non-glycosylated flavonoid with anti-flammatory activities.

    Cellular Effect
    Cell Line Type Value Description References
    A2780 IC50
    > 20 μg/mL
    Compound: 4',5-dihydroxy-7-methoxyflavone
    Cytotoxicity against human A2780 cells
    Cytotoxicity against human A2780 cells
    [PMID: 15217279]
    A549 IC50
    0.4 μg/mL
    Compound: Genkwanin
    Cytotoxicity against human A549 cells by SRB assay
    Cytotoxicity against human A549 cells by SRB assay
    [PMID: 31784199]
    Col2 ED50
    > 20 μg/mL
    Compound: genkwanin
    Cytotoxicity against human Col2 cells
    Cytotoxicity against human Col2 cells
    [PMID: 17279798]
    HCT-15 IC50
    0.4 μg/mL
    Compound: Genkwanin
    Cytotoxicity against human HCT15 cells by SRB assay
    Cytotoxicity against human HCT15 cells by SRB assay
    [PMID: 31784199]
    HUVEC ED50
    > 20 μg/mL
    Compound: genkwanin
    Cytotoxicity against human HUVEC cells
    Cytotoxicity against human HUVEC cells
    [PMID: 17279798]
    HeLa IC50
    8.1 μM
    Compound: Genkwanin
    Cytotoxicity against human HeLa cells assessed as reduction in cell viability incubated for 48 hrs by MTT assay
    Cytotoxicity against human HeLa cells assessed as reduction in cell viability incubated for 48 hrs by MTT assay
    [PMID: 31784199]
    KB IC50
    16.4 μg/mL
    Compound: 7, Genkwanin
    Cytotoxicity against human KB cells
    Cytotoxicity against human KB cells
    [PMID: 8759170]
    KB IC50
    8.7 μg/mL
    Compound: 6, genkwanin
    Cytotoxicity against human KB cells
    Cytotoxicity against human KB cells
    [PMID: 8759170]
    LNCaP ED50
    > 20 μg/mL
    Compound: genkwanin
    Cytotoxicity against human LNCaP cells
    Cytotoxicity against human LNCaP cells
    [PMID: 17279798]
    Lu1 ED50
    > 20 μg/mL
    Compound: genkwanin
    Cytotoxicity against human Lu1 cells
    Cytotoxicity against human Lu1 cells
    [PMID: 17279798]
    MCF-10A IC50
    75 μM
    Compound: Genkwanin
    Cytotoxicity against human MCF-10A cells assessed as inhibition of cell growth by MTT assay
    Cytotoxicity against human MCF-10A cells assessed as inhibition of cell growth by MTT assay
    [PMID: 33257172]
    MCF7 IC50
    10.3 μM
    Compound: Genkwanin
    Cytotoxicity against human MCF7 cells assessed as reduction in cell viability incubated for 48 hrs by MTT assay
    Cytotoxicity against human MCF7 cells assessed as reduction in cell viability incubated for 48 hrs by MTT assay
    [PMID: 31784199]
    MDA-MB-468 IC50
    1.6 μM
    Compound: Genkwanin
    Antiproliferative activity against human MDA-MB-468 cells assessed as inhibition of cell growth by MTT assay
    Antiproliferative activity against human MDA-MB-468 cells assessed as inhibition of cell growth by MTT assay
    [PMID: 33257172]
    MOLM-13 IC50
    > 10 μM
    Compound: 16
    Cytotoxicity against human MOLM-13 cells assessed as reduction in cell viability after 72 hrs by MTT assay
    Cytotoxicity against human MOLM-13 cells assessed as reduction in cell viability after 72 hrs by MTT assay
    [PMID: 33026809]
    MV4-11 IC50
    > 10 μM
    Compound: 16
    Cytotoxicity against human MV4-11 cells assessed as reduction in cell viability after 72 hrs by MTT assay
    Cytotoxicity against human MV4-11 cells assessed as reduction in cell viability after 72 hrs by MTT assay
    [PMID: 33026809]
    P388 IC50
    10 μg/mL
    Compound: 6, genkwanin
    Cytotoxicity against mouse P388 cells
    Cytotoxicity against mouse P388 cells
    [PMID: 8759170]
    RAW264.7 IC50
    5.64 μM
    Compound: 14
    Anti-inflammatory activity in LPS-stimulated mouse RAW264.7 cells assessed as inhibition of NO production incubated for 24 hrs by Griess reagent based assay
    Anti-inflammatory activity in LPS-stimulated mouse RAW264.7 cells assessed as inhibition of NO production incubated for 24 hrs by Griess reagent based assay
    [PMID: 37683361]
    SK-MEL-2 IC50
    0.4 μg/mL
    Compound: Genkwanin
    Cytotoxicity against human SK-MEL-2 cells by SRB assay
    Cytotoxicity against human SK-MEL-2 cells by SRB assay
    [PMID: 31784199]
    SK-OV-3 IC50
    0.4 μg/mL
    Compound: Genkwanin
    Cytotoxicity against human SKOV3 cells by SRB assay
    Cytotoxicity against human SKOV3 cells by SRB assay
    [PMID: 31784199]
    TERT-RPE1 ED50
    3.9 μg/mL
    Compound: genkwanin
    Cytotoxicity against human TERT-RPE1 cells
    Cytotoxicity against human TERT-RPE1 cells
    [PMID: 17279798]
    XF498 IC50
    0.4 μg/mL
    Compound: Genkwanin
    Cytotoxicity against human XF498 cells by SRB assay
    Cytotoxicity against human XF498 cells by SRB assay
    [PMID: 31784199]
    In Vitro

    Cell viability analysis shows that Genkwanin does not affect the cell viability up to a concentration of 50 μM. Genkwanin inhibits the LPS-induced production of NO in a concentration-dependent manner. iNOS only expresses in the present of external stimulus. Genkwanin could not significantly affect the activity of iNOS. The effect of Genkwanin on the production of proinflammatory cytokines is examined. Genkwanin suppresses the productions of TNF-a, IL-1b and IL-6 in LPS stimulated RAW264.7 macrophages in a concentration-dependent manner. Genkwanin significantly suppresses the AP-1 signaling pathway but has little effect on the NF-kB signaling pathway. It is indicated that Genkwanin suppresses the phosphorylation of p38 and JNK in a concentration-dependent manner, but little affects ERK1/2 phosphorylation. Originally identified as an immediate early gene, MKP-1 is then found to be a dual specificity phosphatase acting as a negative regulator of ERK1/2, JNK and p38 MAPK activities, with predominant effects on the latter two. Pretreatment with Genkwanin markedly up-regulates the expression of MKP-1 without affecting MKP-1 mRNA[1].

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

    Molecular Weight

    284.26

    Formula

    C16H12O5

    CAS No.
    Appearance

    Solid

    Color

    Light yellow to yellow

    SMILES

    O=C1C=C(C2=CC=C(O)C=C2)OC3=CC(OC)=CC(O)=C13

    Structure Classification
    Initial Source
    Shipping

    Room temperature in continental US; may vary elsewhere.

    Storage

    4°C, protect from light

    *In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)

    Solvent & Solubility
    In Vitro: 

    DMSO : 31.25 mg/mL (109.93 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 3.5179 mL 17.5895 mL 35.1791 mL
    5 mM 0.7036 mL 3.5179 mL 7.0358 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 (protect from light). 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
    ×
    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: ≥ 0.5 mg/mL (1.76 mM); Clear solution

      This protocol yields a clear solution of ≥ 0.5 mg/mL (saturation unknown).

      Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (5.0 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: 0.5 mg/mL (1.76 mM); Suspended solution; Need ultrasonic

      This protocol yields a suspended solution of 0.5 mg/mL. Suspended solution can be used for oral and intraperitoneal injection.

      Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (5.0 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).

    *In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)

    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: 99.52%

    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 (protect from 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
    DMSO 1 mM 3.5179 mL 17.5895 mL 35.1791 mL 87.9477 mL
    5 mM 0.7036 mL 3.5179 mL 7.0358 mL 17.5895 mL
    10 mM 0.3518 mL 1.7590 mL 3.5179 mL 8.7948 mL
    15 mM 0.2345 mL 1.1726 mL 2.3453 mL 5.8632 mL
    20 mM 0.1759 mL 0.8795 mL 1.7590 mL 4.3974 mL
    25 mM 0.1407 mL 0.7036 mL 1.4072 mL 3.5179 mL
    30 mM 0.1173 mL 0.5863 mL 1.1726 mL 2.9316 mL
    40 mM 0.0879 mL 0.4397 mL 0.8795 mL 2.1987 mL
    50 mM 0.0704 mL 0.3518 mL 0.7036 mL 1.7590 mL
    60 mM 0.0586 mL 0.2932 mL 0.5863 mL 1.4658 mL
    80 mM 0.0440 mL 0.2199 mL 0.4397 mL 1.0993 mL
    100 mM 0.0352 mL 0.1759 mL 0.3518 mL 0.8795 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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    Cat. No.:
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