tcsc1349 ZM 306416

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Product Description

ZM-306416 (CB 676475) is a potent inhibitor of VEGFR with IC50s of 0.1 and 2 μM for KDR and Flt, respectively. ZM-306416 is also a EGFR inhibitor with an IC50 of <10 nM.

IC50 & Target: IC50: 0.1 μM (KDR), 2 μM (Flt)[1], <10 nM (EGFR)[2]

In Vitro: ZM-306416 selective anti-proliferative effect toward the EGFR addicted NSCLC cell lines H3255 and HCC4011 (IC50=0.09±0.007 μM and 0.072±0.001 μM respectively), while sparing the wild type EGFR cell lines A549 and H2030 (IC50>10 μM). ZM-306416 is also found to inhibit the ABL in vitro kinase activity with a less potent IC50 value of 1.3±0.2 μM toward the ABL kinase[2].

Information

CAS No690206-97-4
FormulaC16H13ClFN3O2
Clinical Informationclinicalinformation
PathwayProtein Tyrosine Kinase/RTK
TargetVEGFR

Specifications

Purity / Grade>98%
SolubilityDMSO : 50 mg/mL (149.82 mM; Need ultrasonic); H2O : < 0.1 mg/mL (insoluble)
Smilessmiles

Misc Information

Alternative NamesCB 676475
Observed Molecular Weight333.74
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