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Damnacanthal is a natural anthraquinone compound with potential anticancer, anti-inflammatory, antioxidant, anti-malarial, and antiviral effects.Damnacanthal inhibits a variety of protein kinases such as LIMK1 (IC50=0.8 μM), LIMK2 (IC50=1.5 μM), and Lck (IC50=17 nM), and inhibits the growth of human hepatocellular carcinoma (SKHep-1) and human breast cancer (MCF-7) cells.

| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 1 mg | $800 | Inquiry | Inquiry |
| Description | Damnacanthal is a natural anthraquinone compound with potential anticancer, anti-inflammatory, antioxidant, anti-malarial, and antiviral effects.Damnacanthal inhibits a variety of protein kinases such as LIMK1 (IC50=0.8 μM), LIMK2 (IC50=1.5 μM), and Lck (IC50=17 nM), and inhibits the growth of human hepatocellular carcinoma (SKHep-1) and human breast cancer (MCF-7) cells. |
| Targets&IC50 | p56lck autophosphorylation:46 nM (IC50), Phosphorylation of exogenous substrates by p56lck:220 nM (IC50) |
| In vitro | Methods: Damnacanthal (100nM, 1, 10, 100μM, 1, 2, 4 days) was used to treat HCT-116 and SW480 cells to study its antiproliferative effects on human colorectal cancer cell types. Results: Treatment of HCT-116 cells with Damnacanthal resulted in a significant decrease in cell proliferation at 1 μM (P < 0.05), 10 μM (P < 0.01), and 100 μM (P < 0.01) after 4 days of treatment; SW480 cells also showed a significant decrease in cell proliferation at 10 μM (P < 0.05) and 100 μM (P < 0.001) after 4 days of treatment with Damnacanthal; Damnacanthal had a cytotoxic effect on colorectal cancer cells in both p53 wild-type (HCT-116) and p53 mutant (SW480) cells. Methods: HCT-116 cells were treated with Damnacanthal (1, 10, 50 μM) to determine its possible inhibitory effects on cell cycle progression and apoptosis, and caspase 3/7 activity was measured. Results: Treatment of HCT-116 cells with Damnacanthal (50 μM) resulted in a significant enrichment of cells in the S/G1 and G2/G1 phases. Treatment of HCT-116 cells with Damnacanthal (10 μM) significantly increased caspase 3/7 activity. [2] |
| In vivo | Damnacanthal (10-100 mg/kg, oral, 10-300 minutes) treatment of mice showed a dose-dependent and significant antinociceptive effect in the formalin test, and mice treated with Damnacanthal (100 mg/kg) significantly inhibited histamine-induced paw edema[3]. |
| Synonyms | Damnacantal |
| Molecular Weight | 282.25 |
| Formula | C16H10O5 |
| Cas No. | 477-84-9 |
| Smiles | O=CC1=C(O)C=C2C(=O)C=3C=CC=CC3C(=O)C2=C1OC |
| Relative Density. | 1.461g/cm3 |
| Storage | store at low temperature,keep away from direct sunlight,keep away from moisture | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. | |||||||||||||||
| Solubility Information | DMSO: 2 mg/mL (7.09 mM), Sonication is recommended. | |||||||||||||||
Solution Preparation Table | ||||||||||||||||
DMSO
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Dissolve 2 mg of the compound in 100 μL DMSO
to obtain a stock solution at a concentration of 20 mg/mL . If the required concentration exceeds the compound's known solubility, please contact us for technical support before proceeding.
1) Add 100 μL of the DMSO
stock solution to 400 μL PEG300
and mix thoroughly until the solution becomes clear.
2) Add 50 μL Tween 80 and mix well until fully clarified.
3) Add 450 μL Saline,PBS or ddH2O
and mix thoroughly until a homogeneous solution is obtained.
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