Model: | MOS639089-54-6 |
Place of Origin: | Sichuan,China (Mainland) |
Brand: | MOSINTER |
Molecular Formula: | C23H28N8OS |
Molecular Weight: | 464.59 |
Content: | ≥99% |
Specification: | CP/USP/EP |
Appearance: | White to off-white solid powder |
Structure: | 1 H-NMR and MS spectrum of the sample correspond to the data reported in the literature |
Solubility: | DMSO 90 mg/mL; Water <1 mg/mL; Ethanol <1 mg/mL |
Shipping condition: | Ambient temperature |
Self life: | At least 5 years if properly stored. |
Tozasertib ( CAS: 639089-54-6)
Item | Index |
Molecular Formula | C23H28N8OS |
Molecular Weight | 464.59 |
Specification | CP/USP/EP |
Content | ≥99% |
Tozasertib, also known as VX-680, MK0457 or VE465, is a synthetic, small-molecule Aurora kinase inhibitor with potential antitumor activity. Tozasertib binds to and inhibits Aurora kinases (AKs), thereby inducing apoptosis in tumor cells in which AKs are overexpressed. AKs, a family of serine-threonine kinases, are essential for mitotic progression, spindle formation, centrosome maturation, chromosomal segregation, and cytokinesis.
Details
Although its multi-kinase profile, VX-680 induces similar cytotoxicity with IC50 of approximately 300 nM and exhibits an AUR B-like inhibitory phenotype of G2/M arrest, endoreduplication and apoptosis in BaF3 cells transfected with ABL or FLT-3 (mutant and wild type) kinases. VX-680 prevents the CAL-62 proliferation in a time-dependent manner. VX-680 treatment for 14 days significantly decreases the number and size of colonies by approximately 70% in the 8305C and 90% in the CAL-62, 8505C and BHT-101. Treatment of the different ATC cells with VX-680 inhibits proliferation with the IC50 between 25 and 150 ?nM. The VX-680 significantly impairs the ability of the different cell lines to form colonies in soft agar. Analysis of caspase-3 activity indicates that VX-680 induces apoptosis in the different cell lines. CAL-62 cells exposed for 12? hours to VX-680 showed an accumulation of cells with ≥4N DNA content. Time-lapse analysis demonstrates that VX-680-treated CAL-62 cells exit metaphase without dividing. Moreover, histone H3 phosphorylation is abrogated following VX-680 treatment.VX-680 has significant inhibitory activity against BCR-Abl bearing the T315I mutation in patient-derived samples.
You must be logged in to post a review.
Reviews
There are no reviews yet.