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AG-1478

AG-1478
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Purity:99.71%
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AG-1478

Catalog No. T2047Cas No. 153436-53-4
AG-1478 (NSC-693255) (Tyrphostin AG-1478) is a selective EGFR inhibitor.
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Pack SizePriceAvailabilityQuantity
5 mg$45In Stock
10 mg$61In Stock
25 mg$114In Stock
50 mg$207In Stock
100 mg$288In Stock
200 mg$374In Stock
1 mL x 10 mM (in DMSO)$50In Stock
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Product Introduction

Bioactivity
Description
AG-1478 (NSC-693255) (Tyrphostin AG-1478) is a selective EGFR inhibitor.
In vitro
Co-administration of 0.4 mg AG-1478 with a single dose of 25 μCi 90Y-CHX-A''-DTPA-hu3S193 results in significantly enhanced potency compared to the drugs administered separately. AG-1478 blocks phosphorylation of EGFR at tumor sites and inhibits growth in xenograft models of A431 cells overexpressing wt EGFR and glioma expressing de2-7 EGFR. Even subtherapeutic doses of AG-1478 significantly increase the potency of cytotoxic drugs. The combination of AG-1478 and temozolomide shows synergistic antitumor activity against human glioma xenografts.
In vivo
At a concentration of 0.25 μM, AG-1478 effectively inhibits Ang II, Ca2+ ionophore, and EGF-induced MAPK activation in VSMCs, without affecting fosinopril or platelet-derived growth factor-BB (PDGF-BB)-induced MAPK activation. AG-1478 also suppresses EGF-induced mitosis in BaF/ERX and LIM1215 cells, with IC50 values of 0.07 μM and 0.2 μM, respectively. Furthermore, AG-1478 inhibits the function of ABC (ATP-binding cassette) transport proteins, such as ABCB1 and ABCG2, showing a more significant effect on ABCG2. In comparison to cells expressing endogenous wild-type EGFR or overexpressing exogenous wild-type EGFR (with IC50 values of 34.6 μM and 48.4 μM respectively), AG-1478 preferentially inhibits U87 mg cells expressing ΔEGFR, with an IC50 of 8.7 μM. It also preferentially inhibits tyrosine kinase activity and autophosphorylation of ΔEGFR over endogenous or overexpressed exogenous wild-type EGFR.
Cell Research
Cells are exposed to different concentrations of AG-1478 for 72 hours in 96-well plates. The effects of AG-1478 on cell growth are examined using an Alamar Blue assay. A 20-μL aliquot of Alamar Blue is added to each well, and its absorbance is determined using a Spectromax Scanning Micro plate Reader. The effects of AG-1478 are expressed as percentage of growth inhibition using untreated cells as the control (0% inhibition). Cellular DNA synthesis is determined using a [3H]thymidine incorporation assay. (Only for Reference)
AliasAG1478, NSC 693255, Tyrphostin AG-1478
Chemical Properties
Molecular Weight315.75
FormulaC16H14ClN3O2
Cas No.153436-53-4
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year
Solubility Information
Ethanol: 11 mg/mL (34.8 mM)
H2O: < 1 mg/mL (insoluble or slightly soluble)
DMSO: 4.23 mg/mL (13.4 mM)
Solution Preparation Table
Ethanol/DMSO
1mg5mg10mg50mg
1 mM3.1671 mL15.8353 mL31.6706 mL158.3531 mL
5 mM0.6334 mL3.1671 mL6.3341 mL31.6706 mL
10 mM0.3167 mL1.5835 mL3.1671 mL15.8353 mL
Ethanol
1mg5mg10mg50mg
20 mM0.1584 mL0.7918 mL1.5835 mL7.9177 mL
50 mM0.0633 mL0.3167 mL0.6334 mL3.1671 mL
100 mM0.0317 mL0.1584 mL0.3167 mL1.5835 mL

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