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  3. Physcion

Physcion  (Synonyms: Parietin; Rheochrysidin)

Cat. No.: HY-N0108 Purity: 99.40%
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Physcion (Parietin), an anthraquinone derivative derived from the traditional Chinese medicine rhubarb, is an effective oral active 6-phosphogluconate dehydrogenase inhibitor with blood-brain barrier permeability, with IC50 and Kd values of 38.5 μM and 26.0 μM, respectively. Additionally, Physcion is an inhibitor of the <>bTLR4/NF-κB signaling pathway, exhibiting anti-inflammatory, antibacterial, and anticancer effects, and can induce Apoptosis and Autophagy in cancer cells.

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CAS No. : 521-61-9

사이즈 가격 재고 수량
5 mg 해외재고보유
10 mg 해외재고보유
25 mg 해외재고보유
50 mg 해외재고보유
100 mg 해외재고보유
200 mg   견적 받기  
500 mg   견적 받기  

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고객리뷰

Based on 8 publication(s) in Google Scholar

Other Forms of Physcion:

Top Publications Citing Use of Products

    Physcion purchased from MedChemExpress. Usage Cited in: Mol Cancer. 2025 Mar 26;24(1):97.  [Abstract]

    The cell viability of KYSE-30 and KYSE-410 cells was evaluated after treatment with various concentrations of Physcion (20, 40, 60, 80 μM) for 24 to 72 h.

    Physcion purchased from MedChemExpress. Usage Cited in: Mol Cancer. 2025 Mar 26;24(1):97.  [Abstract]

    Intracellular ROS levels in ESCC cells fluctuated after 48 h of Physcion (20, 40 μM) treatment.

    Physcion purchased from MedChemExpress. Usage Cited in: Mol Cancer. 2025 Mar 26;24(1):97.  [Abstract]

    Western blot analysis revealed a reduction in CDK2 protein expression in ESCC cells following Physcion (20, 40 μM) treatment.

    Physcion purchased from MedChemExpress. Usage Cited in: Mol Cancer. 2025 Mar 26;24(1):97.  [Abstract]

    The effect of Physcion (20, 40 μM) on DNA synthesis in ESCC cells was detected using an EdU staining assay.

    Physcion purchased from MedChemExpress. Usage Cited in: Mol Cancer. 2025 Mar 26;24(1):97.  [Abstract]

    Effects of physcion combined with metformin on the growth of ESCC in vivo. The changes in body weight and tumor volume in nude mice after administration of Physcion (20 mg/kg) and Metformin (200 mg/kg) as single drugs or in combination.

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    • Biological Activity

    • 순도&문서

    • References

    • 고객리뷰

    제품 설명

    Physcion (Parietin), an anthraquinone derivative derived from the traditional Chinese medicine rhubarb, is an effective oral active 6-phosphogluconate dehydrogenase inhibitor with blood-brain barrier permeability, with IC50 and Kd values of 38.5 μM and 26.0 μM, respectively. Additionally, Physcion is an inhibitor of the <>bTLR4/NF-κB signaling pathway, exhibiting anti-inflammatory, antibacterial, and anticancer effects, and can induce Apoptosis and Autophagy in cancer cells[1][2][3][4][5].

    IC50 & Target

    TLR4

     

    Cellular Effect
    Cell Line Type Value Description References
    A549 IC50
    1.5 μM
    Compound: 80
    Antiproliferative activity against human A549 cells assessed as reduction in cell viability measured after 72 hrs by sulforhodamine B assay
    Antiproliferative activity against human A549 cells assessed as reduction in cell viability measured after 72 hrs by sulforhodamine B assay
    [PMID: 33691166]
    A549 IC50
    > 100 μg/mL
    Compound: 6
    Antiproliferative activity against human A549 cells assessed as growth inhibition after 48 hrs by MTT assay
    Antiproliferative activity against human A549 cells assessed as growth inhibition after 48 hrs by MTT assay
    [PMID: 26995526]
    HCT-116 IC50
    19 μM
    Compound: 2
    Cytotoxicity against MDR1 Pgp under-expressing human HCT116 cells after 24 hrs by MTT assay
    Cytotoxicity against MDR1 Pgp under-expressing human HCT116 cells after 24 hrs by MTT assay
    [PMID: 17949858]
    HT-29 IC50
    > 100 μg/mL
    Compound: 6
    Antiproliferative activity against human HT-29 cells assessed as growth inhibition after 48 hrs by MTT assay
    Antiproliferative activity against human HT-29 cells assessed as growth inhibition after 48 hrs by MTT assay
    [PMID: 26995526]
    HUVEC IC50
    > 100 μg/mL
    Compound: 6
    Antiproliferative activity against human HUVEC cells assessed as growth inhibition after 48 hrs by MTT assay
    Antiproliferative activity against human HUVEC cells assessed as growth inhibition after 48 hrs by MTT assay
    [PMID: 26995526]
    HepG2 IC50
    77.3 μM
    Compound: 2
    Cytotoxicity against MDR1 Pgp overexpressing human HepG2 cells after 24 hrs by MTT assay
    Cytotoxicity against MDR1 Pgp overexpressing human HepG2 cells after 24 hrs by MTT assay
    [PMID: 17949858]
    HepG2 2.2.15 IC50
    300 μg/mL
    Compound: 53
    Antiviral activity against Hepatitis B virus infected in human HepG2.2.15 cells assessed as decrease in HBV DNA production
    Antiviral activity against Hepatitis B virus infected in human HepG2.2.15 cells assessed as decrease in HBV DNA production
    [PMID: 24549242]
    HepG2 2.2.15 IC50
    300 μg/mL
    Compound: 53
    Antiviral activity against Hepatitis B virus infected in human HepG2.2.15 cells assessed as decrease in HBV e antigen secretion
    Antiviral activity against Hepatitis B virus infected in human HepG2.2.15 cells assessed as decrease in HBV e antigen secretion
    [PMID: 24549242]
    HepG2 2.2.15 IC50
    300 μg/mL
    Compound: 53
    Antiviral activity against Hepatitis B virus infected in human HepG2.2.15 cells assessed as decrease in HBV surface antigen secretion
    Antiviral activity against Hepatitis B virus infected in human HepG2.2.15 cells assessed as decrease in HBV surface antigen secretion
    [PMID: 24549242]
    KB ED50
    1.55 μg/mL
    Compound: 2
    Cytotoxicity against human KB cells
    Cytotoxicity against human KB cells
    10.1021/np50085a021
    MCF7 IC50
    > 100 μg/mL
    Compound: 6
    Antiproliferative activity against human MCF7 cells assessed as growth inhibition after 48 hrs by MTT assay
    Antiproliferative activity against human MCF7 cells assessed as growth inhibition after 48 hrs by MTT assay
    [PMID: 26995526]
    NCI-H157 IC50
    3 μM
    Compound: 80
    Antiproliferative activity against human NCI-H157 cells assessed as reduction in cell viability measured after 72 hrs by sulforhodamine B assay
    Antiproliferative activity against human NCI-H157 cells assessed as reduction in cell viability measured after 72 hrs by sulforhodamine B assay
    [PMID: 33691166]
    PLC-PRF-5 ED50
    1.44 μg/mL
    Compound: 2
    Cytotoxicity against human PLC/PRF/5 cells
    Cytotoxicity against human PLC/PRF/5 cells
    10.1021/np50085a021
    In Vitro

    Physcion (10 or 20 μM, 48 h) induces apoptosis and autophagy in human nasopharyngeal carcinoma (CNE2 cells)[2].
    Physcion (10-40 μM, 24 h) attenuates OGD/R (oxygen-glucose deprivation/reperfusion)-induced neuronal damage and inflammatory response in SH-SY5Y cells[3].

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

    Apoptosis Analysis[2]

    Cell Line: The nasopharyngeal carcinoma cell line CNE2
    Concentration: 10 or 20 μM
    Incubation Time: 48 h
    Result: Induced apoptosis in CNE2 cells in a dose-dependent manner.

    Western Blot Analysis[2]

    Cell Line: The nasopharyngeal carcinoma cell line CNE2
    Concentration: 10 or 20 μM
    Incubation Time: 48 h
    Result: Significantly increased the level of LC3B-II, which means physcion induced autophagy in CNE2 cells.

    Western Blot Analysis[3]

    Cell Line: Oxygen-glucose deprivation/reperfusion (OGD/R)-induced SH-SY5Y cells
    Concentration: 40 μM
    Incubation Time: 24 h
    Result: Significantly reversed the OGD/R-induced upregulation of TLR4, p-p65, and p-IκB expression.
    In Vivo

    Physcion (20 or 40 mg/kg, p.o., once daily for 7 days) exerts neuroprotective effects by inhibiting the TLR4/NF-κB signaling pathway in an ischemia-reperfusion-induced SD rat model[3].
    Physcion (4 or 9 mg/kg, p.o., once daily for 6 days) effectively alleviates infection symptoms caused by Chlamydia psittaci 6 BCE in SPF chickens[4].

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

    Animal Model: Ischemia-reperfusion (I/R)-induced focal cerebral ischemia model in SD rats[3]
    Dosage: 20 or 40 mg/kg
    Administration: Oral gavage (p.o.), once daily for 7 days
    Result: Significantly reduced the brain water content and the NSS (Neurological Severity Score) in I/R rats, compared to I/R group.
    Obviously decreased areas of infarction compared to I/R group.
    Animal Model: SPF chickens (21 days old) infected intra-laryngeally with Chlamydia psittaci 6 BCE[4]
    Dosage: 4 or 9 mg/kg
    Administration: Oral gavage (p.o.), once daily for 6 days
    Result: Dose-dependently alleviated respiratory distress, air sac and lung lesions, and bacterial load in the spleen in infected chickens.
    분자량

    284.26

    화학식

    C16H12O5

    CAS No.
    Appearance

    Solid

    Color

    Yellow to orange

    SMILES

    O=C1C2=C(C=C(C)C=C2O)C(C3=CC(OC)=CC(O)=C13)=O

    Structure Classification
    Initial Source
    선적

    Room temperature in continental US; may vary elsewhere.

    보관
    Powder -20°C 3 years
    4°C 2 years
    In solvent -80°C 6 months
    -20°C 1 month
    용액&용해도
    In Vitro: 

    THF : 2.5 mg/mL (8.79 mM; ultrasonic and warming and heat to 60°C)

    DMF : 1 mg/mL (3.52 mM; Need ultrasonic)

    Ethanol : < 1 mg/mL (insoluble)

    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. When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.

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

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    Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

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    In Vivo Dissolution Calculator
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    Working solution concentration: mg/mL
    순도&문서

    Purity: 99.40%

    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
    DMF / THF 1 mM 3.5179 mL 17.5895 mL 35.1791 mL 87.9477 mL
    THF 5 mM 0.7036 mL 3.5179 mL 7.0358 mL 17.5895 mL
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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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    상품명:
    Physcion
    Cat. No.:
    HY-N0108
    수량:
    MCE Japan Authorized Agent: