bs-82843C
[Life Science]
(+/-) RK-682
DATASHEET
Formulation Yellow solid
Storage: -20°C
Product Information:
RK-682 is a protein tyrosine phosphatase inhibitor (IC50’s = 54 µM for CD45, 2.0 µM for VHR; did not inhibit cdc25B) originally isolated from the fermentation of Streptomyces sp. 88-682.1 Inhibits cell cycle at G1/S. RK-682 has also been shown to inhibit PLA2 (IC50 = 16 µM)2, HIV-1 protease (IC50 = 84 µM)3, and heparanase (IC50 = 17 µM)4. Natural RK-682 (R-isomer) and synthetic racemic material have identical phosphatase activity.5 Care should be taken when using RK-682 in the presence of metal salts – RK-682 readily forms metal complexes that affects its phosphatase inhibitory activity.6 RK-682 has been identified as a potential promiscuous inhibitor.7
Description:
CAS Number: 150627-37-5<br></br>Chemical Name: 3-Hexadecanoyl-5-hydroxymethyltetronic acid<br></br>Molecular weight: 368.52<br></br>Formula: C21H36O5<br></br>Solubility: DMSO (25 mg/ml) Ethanol (10 mg/ml)<br></br>Physical Properties: Off-white or Yellow solid<br></br>Purity: 98% by TLC, NMR (Conforms)
Size: 1 mg,200 µg 200 µg
Applications: Life Science()
For research use only. Not intended for diagnostic or therapeutic use.