1,6,7-Trihydroxyxanthone
1,6,7-Trihydroxyxanthone is a potent anticancer agent. 1,6,7-Trihydroxyxanthone inhibits cell proliferation and induces cell Apoptosis. 1,6,7-Trihydroxyxanthone decreases Bmi-1 expressio and increases the protein levels expression of P14, P16.
For research use only. We do not sell to patients.
- CAS No.: 25577-04-2
- Formula: C13H8O5
- Molecular Weight:244.20
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Storage:
Please store the product under the recommended conditions in the Certificate of Analysis.
Biological Activity
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Cell Line
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Type | Value | Description | References |
|---|---|---|---|---|
| COLO 320 | IC50 |
85.1 μM
Compound: 45375
|
Antiproliferative activity against human COLO320 cells after 48 hrs by CCK8 assay
Antiproliferative activity against human COLO320 cells after 48 hrs by CCK8 assay
|
[PMID: 28376372] |
| HepG2 | IC50 |
83.8 μM
Compound: 45375
|
Antiproliferative activity against human HepG2 cells after 48 hrs by CCK8 assay
Antiproliferative activity against human HepG2 cells after 48 hrs by CCK8 assay
|
[PMID: 28376372] |
| K562 | IC50 |
155.7 μM
Compound: 45375
|
Antiproliferative activity against human K562 cells after 48 hrs by CCK8 assay
Antiproliferative activity against human K562 cells after 48 hrs by CCK8 assay
|
[PMID: 28376372] |
| MCF7 | IC50 |
101 μM
Compound: 45375
|
Antiproliferative activity against human MCF7 cells after 48 hrs by CCK8 assay
Antiproliferative activity against human MCF7 cells after 48 hrs by CCK8 assay
|
[PMID: 28376372] |
| MDA-MB-231 | IC50 |
65.9 μM
Compound: 45375
|
Antiproliferative activity against human MDA-MB-231 cells after 48 hrs by CCK8 assay
Antiproliferative activity against human MDA-MB-231 cells after 48 hrs by CCK8 assay
|
[PMID: 28376372] |
1,6,7-Trihydroxyxanthone (0-10 µg/mL; 0-72 h) inhibits cell proliferation in HepG2, Bel7404 cells[1].
1,6,7-Trihydroxyxanthone (5 µg/mL; 72 h) induces cell apoptosis in HepG2 cells[1].
1,6,7-Trihydroxyxanthone decreases Bmi-1 expressio and increases the protein levels expression of P14, P16[1].
1,6,7-Trihydroxyxanthone induces MiR-218 up-regulation in HepG2, Bel7404 cells[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Cell Line:HepG2, Bel7404 cells
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Concentration:0, 1.25, 2.5, 5, 10 µg/mL
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Incubation Time:0, 24, 48, 72 h
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Result:Inhibited cell proliferation of HepG2 and Bel7404 in a time- and dose-dependent manner.
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Cell Line:HepG2 cells
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Concentration:5 μg/ml
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Incubation Time:72 h
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Result:Induced cell apoptosis.
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Cell Line:HepG2, Bel7404 cells
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Concentration:
-
Incubation Time:
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Result:Suppressed Bmi-1 expressio and increased the expression of P14, P16 protein levels.
Chemical Information
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CAS No. 25577-04-2
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Molecular Weight 244.20
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Formula C13H8O5
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SMILES
O=C1C2=C(OC3=C1C=C(O)C(O)=C3)C=CC=C2O
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Structure Classification
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Initial Source
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Shipping
Room temperature in continental US; may vary elsewhere.
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Storage
Please store the product under the recommended conditions in the Certificate of Analysis.
Purity & Documentation
References
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)