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CID-5056270
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Catalog No. T23888Cas No. 681173-76-2
CID-5056270 has anticancer activity and can inhibit lung cancer, anal cancer, bladder cancer, cervical cancer, vulvar cancer, penile cancer, Burkitt's lymphoma, breast cancer and bone cancer. It can be used to study hypertension, Alzheimer's disease and arteriosclerosis.
CID-5056270
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Purity: 99.6%
Catalog No. T23888Cas No. 681173-76-2
CID-5056270 has anticancer activity and can inhibit lung cancer, anal cancer, bladder cancer, cervical cancer, vulvar cancer, penile cancer, Burkitt's lymphoma, breast cancer and bone cancer. It can be used to study hypertension, Alzheimer's disease and arteriosclerosis.
| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 1 mg | $197 | In Stock | In Stock | |
| 5 mg | $463 | In Stock | In Stock | |
| 10 mg | $645 | In Stock | In Stock | |
| 25 mg | $953 | In Stock | In Stock | |
| 50 mg | $1,300 | In Stock | In Stock | |
| 100 mg | $1,730 | In Stock | In Stock | |
| 200 mg | $2,330 | - | In Stock | |
| 1 mL x 10 mM (in DMSO) | $469 | In Stock | In Stock |
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
This molecule is a custom-made product. TargetMol has an excellent synthesis team with the experience and capability to provide you with cost-effective products.If you have any questions, please feel free to contact us. We are committed to serving you wholeheartedly.
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:99.6%
Appearance:Solid
Color:White
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Product Introduction
CID-5056270 AI Summary
CID-5056270 is a potent inhibitor of ROCK2, exhibiting an IC50 of 7.2 nM and causing a 91.3% inhibition in certain assays. It also effectively inhibits ROCK1 with an IC50 of 13.0 nM, but shows significantly lower activity against Aurora-A, with an IC50 exceeding 100,000 nM. In rat A7r5 cells, it inhibits myosin light chain bisphosphorylation with an IC50 of 137.0 nM. The compound demonstrates moderate inhibition of PKA, MRCK, and various human CYP enzymes, and affects a wide array of biological targets, including HSD17B4, Tau Fibril Formation, and Aldehyde Dehydrogenase 1, among others. It acts as an agonist of the Thyroid Stimulating Hormone Receptor, increases intracellular cAMP concentrations, and shows cytotoxicity against HeLa cells. Despite its broad bioactivity, CID-5056270 has low metabolic stability in human liver microsomes and exhibits negligible oral bioavailability and limited clearance in rat models..
Note: Summary generated by AI. Data source: ChEMBL 
Bioactivity
Chemical Properties
Storage & Solubility Information
| Description | CID-5056270 has anticancer activity and can inhibit lung cancer, anal cancer, bladder cancer, cervical cancer, vulvar cancer, penile cancer, Burkitt's lymphoma, breast cancer and bone cancer. It can be used to study hypertension, Alzheimer's disease and arteriosclerosis. |
| Molecular Weight | 339.37 |
| Formula | C17H13N3O3S |
| Cas No. | 681173-76-2 |
| Smiles | N(C(=O)C1OC=2C(OC1)=CC=CC2)C3=NC(=CS3)C=4C=CN=CC4 |
| Relative Density. | 1.425 g/cm3 (Predicted) |
| 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: 3.4 mg/mL (10.02 mM), Sonication is recommended.  | ||||||||||||||||||||
Solution Preparation Table | |||||||||||||||||||||
DMSO
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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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