A farnesyltransferase inhibitor. Sensitizes human multiple myeloma cell to proteasome inhibition by blocking degradation of bortezomib-induced aggresomes. Also shown to inhibit the growth of myeloid leukemia cell lines and primary leukemia cells by inducing apoptosis and cell-cycle blockage when combined with rapamycin(R124000).
Melting Point:211-213°C (dec.)
Solubility:Chloroform, Methanol
Specific Rotation:+20.9°C (c=0.7, Methanol)
Method for Determining Identity:Proton NMR, (CDCI3) Spectroscopic and Mass Spectrometric Analysis
TLC Conditions:SiO2; Dichloromethane: Methanol=9:1; Visualized with UV and AMCS; Single spot. Rf=0.45.
Important Note:This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications without the expressed written authorization of United States Biological.
Toxicity and Hazards: All products should be handled by qualified personnel only, trained in laboratory procedures
仕様
Size：5mg
Source Antigen：Synthetic
Grade：Highly Purified
Purity：90%
Form：Supplied as an off-white to pale beige solid.
