OSI-930

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Chemical Information

Product name：OSI-930	Purity：98% min
CAS NO：728033-96-3	Solubility：≥22.15mg/mL in DMSO
Molecular Formula：C₂₂H₁₆F₃N₃O₂S	Package：Package according to customer requirements
Molecular Weight：443.442	Storage：Store at -20℃

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Remarks

OSI-930 is a selective thiophene-derived tyrosine kinase inhibitor with potential antineoplastic activity. Tyrosine kinase inhibitor OSI-930 inhibits stem cell factor receptor (c-Kit) and the vascular endothelial growth factor receptor 2 (VEGFR2), which may result in the inhibition of both tumor cell proliferation and tumor angiogenesis. Both c-Kit and VEGFR2 are overexpressed in a variety of cancers. Check for active clinical trials or closed clinical trials using this agent.

Related Products:

Pexidartinib hcl; Pexidartinib; Telatinib; Avapritinib; Amuvatinib; Dovitinib Lactate; Linifanib; Crenolanib; Motesanib Diphosphate; Motesanib; Sunitinib; Imatinib mesylate; Axitinib; Masitinib; Dovitinib; ISCK03

References

[1]. Garton AJ, et al. OSI-930: a novel selective inhibitor of Kit and kinase insert domain receptor tyrosine kinases with antitumor activity in mouse xenograft models. Cancer Res. 2006, 66(2):1015-1024.

[2]. Lin HL, et al. Inactivation of cytochrome P450 (P450) 3A4 but not P450 3A5 by OSI-930, a thiophene-containing anticancer drug. Drug Metab Dispos. 2011, 39(2), 345-350.