TC-S 7005Potent and selective PLK2 inhibitor CAS# 1082739-92-1 |
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Quality Control & MSDS
Number of papers citing our products
Chemical structure
3D structure
| Cas No. | 1082739-92-1 | SDF | Download SDF |
| PubChem ID | 24971422 | Appearance | Powder |
| Formula | C21H17N3O3 | M.Wt | 359.38 |
| Type of Compound | N/A | Storage | Desiccate at -20°C |
| Solubility | DMSO : 125 mg/mL (347.82 mM; Need ultrasonic) | ||
| Chemical Name | 3-(1,3-benzodioxol-5-yl)-N-[(1S)-1-phenylethyl]-[1,2]oxazolo[5,4-c]pyridin-5-amine | ||
| SMILES | CC(C1=CC=CC=C1)NC2=NC=C3C(=C2)C(=NO3)C4=CC5=C(C=C4)OCO5 | ||
| Standard InChIKey | DAAGOCSHXCDWDY-ZDUSSCGKSA-N | ||
| Standard InChI | InChI=1S/C21H17N3O3/c1-13(14-5-3-2-4-6-14)23-20-10-16-19(11-22-20)27-24-21(16)15-7-8-17-18(9-15)26-12-25-17/h2-11,13H,12H2,1H3,(H,22,23)/t13-/m0/s1 | ||
| General tips | For obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while.Stock solution can be stored below -20℃ for several months. We recommend that you prepare and use the solution on the same day. However, if the test schedule requires, the stock solutions can be prepared in advance, and the stock solution must be sealed and stored below -20℃. In general, the stock solution can be kept for several months. Before use, we recommend that you leave the vial at room temperature for at least an hour before opening it. |
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| About Packaging | 1. The packaging of the product may be reversed during transportation, cause the high purity compounds to adhere to the neck or cap of the vial.Take the vail out of its packaging and shake gently until the compounds fall to the bottom of the vial. 2. For liquid products, please centrifuge at 500xg to gather the liquid to the bottom of the vial. 3. Try to avoid loss or contamination during the experiment. |
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| Shipping Condition | Packaging according to customer requirements(5mg, 10mg, 20mg and more). Ship via FedEx, DHL, UPS, EMS or other couriers with RT, or blue ice upon request. | ||
| Description | Potent and selective polo-like kinase 2 (PLK2) inhibitor (IC50 = 4 nM). Shows selectivity for PLK2 over PLK3 and PLK1 (IC50 values are 24 and 214 nM respectively). Induces mitotic arrest and cell death in HCT 116 colorectal cells. |
TC-S 7005 Dilution Calculator
TC-S 7005 Molarity Calculator
| 1 mg | 5 mg | 10 mg | 20 mg | 25 mg | |
| 1 mM | 2.7826 mL | 13.9128 mL | 27.8257 mL | 55.6514 mL | 69.5642 mL |
| 5 mM | 0.5565 mL | 2.7826 mL | 5.5651 mL | 11.1303 mL | 13.9128 mL |
| 10 mM | 0.2783 mL | 1.3913 mL | 2.7826 mL | 5.5651 mL | 6.9564 mL |
| 50 mM | 0.0557 mL | 0.2783 mL | 0.5565 mL | 1.113 mL | 1.3913 mL |
| 100 mM | 0.0278 mL | 0.1391 mL | 0.2783 mL | 0.5565 mL | 0.6956 mL |
| * Note: If you are in the process of experiment, it's necessary to make the dilution ratios of the samples. The dilution data above is only for reference. Normally, it's can get a better solubility within lower of Concentrations. | |||||
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Design and synthesis of 2-amino-isoxazolopyridines as Polo-like kinase inhibitors.[Pubmed:18790636]
Bioorg Med Chem Lett. 2008 Oct 1;18(19):5186-9.
A series of 2-amino-isoxazolopyridines was designed and synthesized as Polo-like kinase (Plk) inhibitors. Key SAR and crystallographic data are discussed. More advanced analogues inhibit Plk1 with good enzymatic activity and modest cell-based activity. Differential selectivity among the three Plk isoforms is observed.
TC-S 7005 is a Polo-like kinases (Plks) inhibitor with IC50s of 4 nM, 24 nM and 214 nM for Plk2, Plk3, and Plk1, respectively.
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