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NSC745885
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Catalog No. T16354Cas No. 4219-52-7
Alias NSC-745885, NSC 745885
NSC745885 is an antitumor agent non-toxic to normal cells that downregulates EZH2 via proteasome-mediated degradation. It exhibits toxicity against multiple normal and drug-resistant cancer cell lines and may be used in studies of advanced bladder cancer and oral squamous cell carcinoma.
NSC745885
Copy Product Info😃Good
Catalog No. T16354Alias NSC-745885, NSC 745885Cas No. 4219-52-7
NSC745885 is an antitumor agent non-toxic to normal cells that downregulates EZH2 via proteasome-mediated degradation. It exhibits toxicity against multiple normal and drug-resistant cancer cell lines and may be used in studies of advanced bladder cancer and oral squamous cell carcinoma.
| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 1 mg | $68 | 6-8 weeks | 6-8 weeks | |
| 5 mg | Preferential | - | In Stock |
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
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Appearance:Solid
Color:Yellow
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| Description | NSC745885 is an antitumor agent non-toxic to normal cells that downregulates EZH2 via proteasome-mediated degradation. It exhibits toxicity against multiple normal and drug-resistant cancer cell lines and may be used in studies of advanced bladder cancer and oral squamous cell carcinoma. |
| In vitro | NSC745885 (0.5–4 μM; 24/48/72 h) reduced SAS cell density with growth-inhibitory or pro-apoptotic effects. After 72 h treatment, IC50 = 0.85 μM. NSC745885 dose-dependently increased membranin V-positive cells [1]. NSC745885 (0.5–2 μM; 24/48 hours) dose-dependently reduced XIAP protein levels and increased protein levels in SAS cells [1]. |
| In vivo | NSC745885 (intraperitoneal; 2 mg/kg; daily; 10 days) significantly reduced tumor size compared to controls and demonstrated superior safety to Doxorubicin [1]. |
| Synonyms | NSC-745885, NSC 745885 |
| Molecular Weight | 266.27 |
| Formula | C14H6N2O2S |
| Cas No. | 4219-52-7 |
| Smiles | O=C1C=2C=CC=CC2C(=O)C=3C4=NSN=C4C=CC13 |
| Relative Density. | 1.574 g/cm3 (Predicted) |
| Storage | store at low temperature | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. |
| Solubility Information | DMSO: < 1 mg/mL (insoluble) |
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In Vivo Formulation Calculator (Clear solution)
Please enter your animal experiment information in the following box and click Calculate to obtain the stock solution preparation method and in vivo formula preparation method:
For example, if the intended dosage is 10 mg/kg for animals weighing 20 g , with a dosing volume of 100 μL per animal, and a total of 10 animals are to be administered, using a formulation of 
10% DMSO+ 40% PEG300+ 5% Tween 80+ 45% Saline/PBS/ddH2O , the resulting working solution concentration would be 2 mg/mL.Stock Solution Preparation:
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.
Preparation of the In Vivo Formulation:
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.
This example is provided solely to demonstrate the use of the In Vivo Formulation Calculator and does not constitute a recommended formulation for any specific compound. Please select an appropriate dissolution and formulation strategy based on your experimental model and route of administration.
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Please see Inhibitor Handling Instructions for more frequently ask questions. Topics include: how to prepare stock solutions, how to store products, and cautions on cell-based assays & animal experiments, etc
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