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PD166285

Chemical Structure : PD166285

CAS No.: 212391-63-4

PD166285 (PD-166285;PD 166285;PD 0166285)

Catalog No.: PC-60888Not For Human Use, Lab Use Only.

PD166285 (PD 0166285) is a broad-spectrum receptor tyrosine kinase (RTK) inhibitor that inhibits PDGFR-β, EGFR, and FGFR1 and c-Src with IC50 of 7-85 nM, also inhibits the checkpoint kinases Wee1 and Myt1.

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Purity & Documentation Purity: >98% (HPLC) Select Batch:

Biological Activity

PD166285 (PD 0166285) is a broad-spectrum receptor tyrosine kinase (RTK) inhibitor that inhibits PDGFR-β, EGFR, and FGFR1 and c-Src with IC50 of 7-85 nM, also inhibits the checkpoint kinases Wee1 and Myt1.
PD166285  inhibits the formation of microcapillaries on Matrigel-coated plastic at 10 nM.
PD166285 inhibits angiogenesis in mice after oral administration (1-25 mg/kg), significantly prolongs tumor regressions in vivo.

Physicochemical Properties

M.Wt 585.35
Formula C26H27Cl2N5O2.2HCl
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

10 mM in DMSO

Chemical Name/SMILES

6-(2,6-Dichlorophenyl)-2-[[4-[2-(diethylamino)ethoxy]phenyl]amino]-8-methylpyrido[2,3-d]pyrimidin-7(8H)-one dihydrochloride

References

1. Dimitroff CJ, et al. Invest New Drugs. 1999;17(2):121-35.

2. Bansal R, et al. J Neurosci Res. 2003 Nov 15;74(4):486-93.

3. Panek RL, et al. J Pharmacol Exp Ther. 1997 Dec;283(3):1433-44.

4. Wang Y, et al. Cancer Res. 2001 Nov 15;61(22):8211-7.

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