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DpC
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Catalog No. T77614Cas No. 1382469-39-7
DPC is an antitumor compound that inhibits cancer cell proliferation with an IC50 of 0.007-0.096 μM.DPC is involved in a variety of anticancer therapies and can be used in cancer research.
DpC
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Purity: 98.99%
Catalog No. T77614Cas No. 1382469-39-7
DPC is an antitumor compound that inhibits cancer cell proliferation with an IC50 of 0.007-0.096 μM.DPC is involved in a variety of anticancer therapies and can be used in cancer research.
| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 1 mg | $30 | In Stock | In Stock | |
| 5 mg | $68 | In Stock | In Stock | |
| 10 mg | $108 | In Stock | In Stock | |
| 25 mg | $222 | In Stock | In Stock | |
| 50 mg | $355 | In Stock | In Stock | |
| 100 mg | $526 | In Stock | In Stock |
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
All TargetMol products are for research purposes only and cannot be used for human consumption. We do not provide products or services to individuals. Please comply with the intended use and do not use TargetMol products for any other purpose.
Batch Information
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Purity:98.99%
Appearance:Solid
Color:Yellow
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Product Introduction
DpC AI Summary
DpC demonstrates significant antiproliferative activity across various human cancer cell lines, including A549, DMS53, SK-N-MC, MIAPaCa2, PANC1, Capan2, CFPAC-1, MGC-803, HGC-27, SGC-7901, BGC-823, EC9706, MCF7, GES-1, WPMY-1, and PC3. Notably, it exhibits potent effects with IC50 values as low as 4.0 nM in A549 cells and shows a range of cytotoxicity from 5.0 nM to 203.0 nM in a 24-hour MTT assay for different cell lines. The compound also displays a selectivity index, such as 3.7 for PC3 over GES-1 and 5.9 for PC3 over WPMY-1 cells. Moreover, DpC acts as a substrate for P-gp, enhancing ATPase activity at 50 µM and exhibits a selectivity ratio of 8.1 between human KB31 and KBV1 cells overexpressing P-gp.
Additionally, DpC has notable antibacterial properties, particularly against antibiotic-resistant bacteria, including vancomycin-resistant Enterococcus faecium and methicillin-resistant Staphylococcus aureus. It inhibits bacterial enzymes like NDM-1, VIM-2, IMP-1, ImiS, and L1 with nanomolar IC50 values, demonstrating strong and reversible enzyme inhibition and synergistic effects with meropenem. However, it shows cytotoxicity at high concentrations against Vero E6 cells. These diverse bioactivities suggest DpC’s potential as both an anticancer and antibacterial agent..
Note: Summary generated by AI. Data source: ChEMBL 
Bioactivity
Chemical Properties
Storage & Solubility Information
| Description | DPC is an antitumor compound that inhibits cancer cell proliferation with an IC50 of 0.007-0.096 μM.DPC is involved in a variety of anticancer therapies and can be used in cancer research. |
| Molecular Weight | 353.48 |
| Formula | C19H23N5S |
| Cas No. | 1382469-39-7 |
| Smiles | C(=NNC(N(C)C1CCCCC1)=S)(C2=CC=CC=N2)C3=CC=CC=N3 |
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. | |||||||||||||||||||||||||||||||||||
| Solubility Information | DMSO: 50 mg/mL (141.45 mM), Sonication is recommended.  | |||||||||||||||||||||||||||||||||||
| In Vivo Formulation | 10% DMSO+40% PEG300+5% Tween 80+45% Saline: 2 mg/mL (5.66 mM), Sonication is recommended. Please add the solvents sequentially, clarifying the solution as much as possible before adding the next one. Dissolve by heating and/or sonication if necessary. Working solution is recommended to be prepared and used immediately. The formulation provided above is for reference purposes only. In vivo formulations may vary and should be modified based on specific experimental conditions. | |||||||||||||||||||||||||||||||||||
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Calculator
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.
Dose Conversion
You can also refer to dose conversion for different animals. More Dose Conversion
Tech Support
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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