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  3. Oroxylin A

Oroxylin A  (Synonyms: Baicalein 6-methyl ether; 6-Methoxybaicalein)

Cat. No.: HY-N0560 Purity: 99.40%
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Oroxylin A is an active flavonoid compound with strong anti-cancer effects. Oroxylin A inhibits the IL-6/STAT3 pathway and NF-κB signaling, inhibits cell proliferation and induces apoptosis. Oroxylin A inhibits colitis-related carcinogenesis.

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

CAS No. : 480-11-5

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Solid + Solvent (Highly Recommended)
10 mM * 1 mL in DMSO
ready for reconstitution
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Based on 18 publication(s) in Google Scholar

Other Forms of Oroxylin A:

Top Publications Citing Use of Products

    Oroxylin A purchased from MedChemExpress. Usage Cited in: Ecotoxicol Environ Saf. 2024 May:276:116327.  [Abstract]

    Oroxylin A (OA, 1 μg/mL; 46 h) an ngn1 agonist, was used to verify the role of ngn1 in this process to determine whether ROX mediates motor nerve development by inhibiting ngn1. In the presence of OA, ROX-induced motor nerve damage was rescued in transgenic zebrafish Tg(hb9:eGFP).

    Oroxylin A purchased from MedChemExpress. Usage Cited in: Ecotoxicol Environ Saf. 2024 May:276:116327.  [Abstract]

    Oroxylin A (OA, 1 μg/mL; 46 h) treatment restored the downregulated expression of the ngn1 gene caused by ROX exposure in Tg(hb9:eGFP) zebrafish by activating ngn1.

    Oroxylin A purchased from MedChemExpress. Usage Cited in: Ecotoxicol Environ Saf. 2024 May:276:116327.  [Abstract]

    Oroxylin A (OA, 1 μg/mL; 46 h) partially rescued the locomotor behavioral deficits associated with ROX exposure in Tg(hb9:eGFP) zebrafish by activating ngn1.

    Oroxylin A purchased from MedChemExpress. Usage Cited in: J Adv Res. 2024 Jan:55:45-60.  [Abstract]

    Oroxylin A (OA, 150 μM; 48 h) inhibited mitophagy in CCl₄-treated E47 cells with FUNDC1-OE, as evidenced by downregulation of Parkin and BNIP3 as well as upregulation of TIM23, with subtle changes in FUNDC1.

    Oroxylin A purchased from MedChemExpress. Usage Cited in: J Adv Res. 2024 Jan:55:45-60.  [Abstract]

    Effect of Oroxylin A (OA) on cell mitophagy and ferroptosis in CCl4-treated E47 cells with FUNDC1 overexpression. E47 cells were transfected with scrambled or FUNDC1 plasmid for 48 hrs and were then treated DMSO or OA (150 μM; 48 h) prior to exposure to CCl4 for 12 hrs. Representative images of C11-BODIPY staining.

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    • Biological Activity

    • Purity & Documentation

    • References

    • Customer Review

    Description

    Oroxylin A is an active flavonoid compound with strong anti-cancer effects. Oroxylin A inhibits the IL-6/STAT3 pathway and NF-κB signaling, inhibits cell proliferation and induces apoptosis. Oroxylin A inhibits colitis-related carcinogenesis[1][2][3][4][5].

    Cellular Effect
    Cell Line Type Value Description References
    HCT-116 IC50
    33.9 μM
    Compound: 1, Oroxylin A
    Antiproliferative activity against human HCT116 cells after 48 hrs by MTT assay
    Antiproliferative activity against human HCT116 cells after 48 hrs by MTT assay
    [PMID: 22196122]
    HUVEC IC50
    61 μM
    Compound: 5
    Inhibition of trypsin-induced elevation in PAI1 production in HUVEC by ELISA
    Inhibition of trypsin-induced elevation in PAI1 production in HUVEC by ELISA
    [PMID: 9214730]
    HepG2 IC50
    22.7 μM
    Compound: 1, Oroxylin A
    Antiproliferative activity against human HepG2 cells after 48 hrs by MTT assay
    Antiproliferative activity against human HepG2 cells after 48 hrs by MTT assay
    [PMID: 22196122]
    KB IC50
    16.1 μM
    Compound: O, oroxylin-A
    Cytotoxicity against multi-drug resistant human KB cells overexpressing mdr1 after 3 days
    Cytotoxicity against multi-drug resistant human KB cells overexpressing mdr1 after 3 days
    [PMID: 18722769]
    KB IC50
    31.1 μM
    Compound: O, oroxylin-A
    Cytotoxicity against human KB cells after 3 days
    Cytotoxicity against human KB cells after 3 days
    [PMID: 18722769]
    MV4-11 GI50
    5.59 μM
    Compound: 14, Oroxylin
    Cytotoxicity against human MV4-11 cells harboring FLT3 mutation after 72 hrs by tetrazolium based Ez CyTox cell viability assay
    Cytotoxicity against human MV4-11 cells harboring FLT3 mutation after 72 hrs by tetrazolium based Ez CyTox cell viability assay
    [PMID: 23411073]
    RAW264.7 IC50
    16.73 μM
    Compound: 1, oroxylin A
    Cytotoxicity against mouse RAW264.7 cells
    Cytotoxicity against mouse RAW264.7 cells
    [PMID: 22101131]
    RAW264.7 IC50
    48.9 μM
    Compound: 6
    Antiinflammatory activity against LPS-stimulated mouse RAW264.7 cells assessed as reduction in NO production
    Antiinflammatory activity against LPS-stimulated mouse RAW264.7 cells assessed as reduction in NO production
    [PMID: 37778427]
    RS4-11 GI50
    40 μM
    Compound: 14, Oroxylin
    Cytotoxicity against human RS4:11 cells harboring wild type FLT3 after 72 hrs by tetrazolium based Ez CyTox cell viability assay
    Cytotoxicity against human RS4:11 cells harboring wild type FLT3 after 72 hrs by tetrazolium based Ez CyTox cell viability assay
    [PMID: 23411073]
    SW1353 IC50
    > 50 μM
    Compound: 5
    Antiinflammatory activity in PMA-stimulated human SW1353 cells assessed as inhibition of NF-kappaB activation
    Antiinflammatory activity in PMA-stimulated human SW1353 cells assessed as inhibition of NF-kappaB activation
    [PMID: 19555121]
    In Vitro

    Oroxylin A (20 μM; 24 h) inhibits the growth, proliferation, and migration of MDA-MB-231 cells. Oroxylin A also inhibits the invasion of MDA-MB-231 and inhibits its epithelial-to-mesenchymal transition (EMT) process[4].
    Oroxylin A (20 μM; 24 h) also inhibits the expression of pro-inflammatory cytokines and inhibits the NF-κB signaling pathway[4].
    The anti-inflammatory effect of Oroxylin A is abolished by TNF-α[4].

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

    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 2 years
    -20°C 1 year
    Solvent & Solubility
    In Vitro: 

    DMSO : 62.5 mg/mL (219.87 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, 2 years; -20°C, 1 year. When stored at -80°C, please use it within 2 years. When stored at -20°C, please use it within 1 year.

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

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    In Vivo Dissolution Calculator
    Please enter the basic information of animal experiments:

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    Calculation results:
    Working solution concentration: mg/mL
    Purity & Documentation

    Purity: 99.87%

    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, 2 years; -20°C, 1 year. When stored at -80°C, please use it within 2 years. When stored at -20°C, please use it within 1 year.

    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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