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Rigosertib sodium

Chemical Structure : Rigosertib sodium

CAS No.: 592542-60-4

Rigosertib sodium (ON-01910 sodium;ON01910 sodium;ON01910 sodium)

Catalog No.: PC-42851Not For Human Use, Lab Use Only.

Rigosertib sodium (ON 01910.Na) is a potent, non-ATP-competitive PLK1 inhibitor (IC50=9-10 nM), selectively induces mitotic G2/M arrest and apoptosis in cancer cells.

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Biological Activity

Rigosertib sodium (ON 01910.Na) is a potent, non-ATP-competitive PLK1 inhibitor (IC50=9-10 nM), selectively induces mitotic G2/M arrest and apoptosis in cancer cells.
Rigosertib also exhibits inhibitory activity against PDGFR, Abl, and Flt-1, at higher concentrations, inhibits CDK1, Plk2, Src, and Fyn.
Rigosertib demonstrates in vitro cytotoxicity against DU145 and K562 cells with IC50 of 100 and 15 nM.
Rigosertib potently inhibits tumor growth in a variety of xenograft nude mouse models, does not exhibit hematotoxicity, liver damage, or neurotoxicity shows strong synergy with several chemotherapeutic agents.

Physicochemical Properties

M.Wt 473.4719
Formula C21H24NNaO8S
Appearance Solid
CAS No.
Storage
Solide Powder
-20 °C 12 Months; 4°C 6 Months
In Solvent
-80 °C 6 Months; -20°C 6 Months
Shipping
Solubility

H2O: ≥ 52 mg/mL

Chemical Name/SMILES

Glycine, N-[2-methoxy-5-[[[(1E)-2-(2,4,6-trimethoxyphenyl)ethenyl]sulfonyl]methyl]phenyl]-, sodium salt (1:1)

References

1. Reddy MV, et al. J Med Chem. 2011 Sep 22;54(18):6254-76.

2. Gumireddy K, et al. Cancer Cell. 2005 Mar;7(3):275-86.

3. Oussenko IA, et al. Cancer Res. 2011 Jul 15;71(14):4968-76.

4. Chun AW, et al. Cancer Chemother Pharmacol. 2009 Dec;65(1):177-86.

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