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| Product Name | RK 682 |
| Description |
Tyrosine phopshatase inhibitor |
| Purity | >98% (HPLC) |
| CAS No. | 150627-37-5 |
| Molecular Formula | C21H36O5 |
| Molecular Weight | 368.5 |
| Field of Use | Not for use in humans. Not for use in diagnostics or therapeutics. For in vitro research use only. |
Properties
| Storage Temperature | -20ºC |
| Shipping Temperature | Shipped Ambient |
| Product Type | Inhibitor |
| Solubility | Soluble DMSO, heptane and xylene: ≥8 mg/ml |
| Source | Synthetic |
| Appearance | Solid |
| InChI | InChI=1S/C21H36O5/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-17(23)19-20(24)18(16-22)26-21(19)25/h18,22,24H,2-16H2,1H3 |
| InChIKey | KZTSLHQKWLYYAC-UHFFFAOYSA-N |
| Safety Phrases |
Classification: Not a hazardous substance or mixture. Safety Phrases: S22 - Do not breathe dust. S24/25 - Avoid contact with skin and eyes. S36/37/39 - Wear suitable protective clothing, gloves and eye/face protection. |
| Cite This Product | RK 682 (StressMarq Biosciences Inc., Victoria BC CANADA, Catalog # SIH-522) |
Biological Description
| Alternative Names | RK-682, (R)-3-Hexadecanoyl-5-hydroxymethyltetronic acid, (R)-4-Hydroxy-5-(hydroxymethyl)-3-(1-oxohexadecyl)-2(5H)-furanone |
| Research Areas | Cell Signaling |
| PubChem ID | 54685915 |
| Scientific Background | RK 682 is a specific inhibitor of protein tyrosine phosphatase. It is naturally occurring calcium salt of 3-hexadecanoyl-5-hydroxymethyl-tetronic acid. RK 682 has been shown to inhibit cell cycle progression at G1 phase. |
| References | 1. Hamaguchi T., Sudo T., & Osada H. (1995) FEBS Letters. 372(1): 54–58. |
Product Images
Chemical structure of RK 682 (SIH-522), a Tyrosine phopshatase inhibitor. CAS #: 150627-37-5. Molecular Formula: C21H36O5. Molecular Weight: 368.5 g/mol.
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