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PHPS1
🥰Excellent
Catalog No. T28410Cas No. 314291-83-3
Alias PHPS-1, PHPS 1
PHPS1 is an inhibitor of Shp2. PHPS1 efficiently inhibits activation of Erk1/2 by the leukemia-associated Shp2 mutant, Shp2-E76K, and blocks the anchorage-independent growth of a variety of human tumor cell lines.
PHPS1
🥰Excellent
Purity: 99.08%
Catalog No. T28410Alias PHPS-1, PHPS 1Cas No. 314291-83-3
PHPS1 is an inhibitor of Shp2. PHPS1 efficiently inhibits activation of Erk1/2 by the leukemia-associated Shp2 mutant, Shp2-E76K, and blocks the anchorage-independent growth of a variety of human tumor cell lines.
| Pack Size | Price | Availability | Quantity |
|---|---|---|---|
| 1 mg | $39 | In Stock | |
| 5 mg | $89 | In Stock | |
| 10 mg | $139 | In Stock | |
| 25 mg | $297 | In Stock | |
| 50 mg | $469 | In Stock | |
| 100 mg | $712 | In Stock | |
| 500 mg | $1,460 | In Stock | |
| 1 mL x 10 mM (in DMSO) | $127 | In Stock |
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Purity:99.08%
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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.Product Introduction
Bioactivity
Chemical Properties
| Description | PHPS1 is an inhibitor of Shp2. PHPS1 efficiently inhibits activation of Erk1/2 by the leukemia-associated Shp2 mutant, Shp2-E76K, and blocks the anchorage-independent growth of a variety of human tumor cell lines. |
| Targets&IC50 | PTP1B Q:0.47 μM(Ki), Shp2 (R362K):5.8 μM(Ki;Shp2-R362K), PTP1B:5.8 μM(Ki), SHP1:10.7 μM(Ki), SHP2:0.73 μM(Ki) |
| In vitro | PHPS1 (30 μM; 6 days) inhibits human tumor cell proliferation, and at concentrations of 5-20 μM (5-360 minutes), it inhibits Erk1/2 phosphorylation in a dose-dependent manner without affecting Akt and Stat3 phosphorylation[1]. |
| In vivo | PHPS1 (3 mg/kg; i.p. injection; administered daily during the final week of a high-fat diet) reduces susceptibility to atherosclerosis in Ldlr-/- mice[2]. |
| Alias | PHPS-1, PHPS 1 |
| Molecular Weight | 465.44 |
| Formula | C21H15N5O6S |
| Cas No. | 314291-83-3 |
| Smiles | OS(=O)(=O)c1ccc(N\N=C2/C(=O)N(N=C2c2ccc(cc2)[N+]([O-])=O)c2ccccc2)cc1 |
| Relative Density. | 1.54 g/cm3 (Predicted) |
Storage & Solubility Information
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. | |||||||||||||||||||||||||
| Solubility Information | DMSO: 16.25 mg/ml (34.91 mM)  | |||||||||||||||||||||||||
Solution Preparation Table | ||||||||||||||||||||||||||
DMSO
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Please enter your animal experiment information in the following box and click Calculate to obtain the mother liquor preparation method and in vivo formula preparation method:
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DMSO+30% PEG300+5% Tween 80+60% ddH2O. So your working solution concentration is 2 mg/mL。Mother liquor preparation method: 2 mg of drug dissolved in 50 μL DMSO (mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.
(mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.Preparation method for in vivo formula: Take 50 μL DMSO main solution, add 300 μLPEG300 mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2O mix well and clarify
main solution, add 300 μLPEG300 mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2O mix well and clarifyFor Reference Only. Please develop an appropriate dissolution method based on your laboratory animals and route of administration.
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