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AG-490

Catalog No. S1143 Product Citations2 Product Citation(s)
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$ 50 Yes
$ 100 Yes
 
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AG-490 Chemical Structure

Bio Information

AG 490 is a potent epidermal growth factor receptor kinase autophosphorylation inhibitor with an IC50 of 100 nM and 56.8μM for EGFR and JAK, respectively. It inhibits cytokine-independent cell growth in vitro and tumor cell invasion in vivo. It selectively blocks leukemic cell growth in vitro and in vivo by inducing programmed cell death, with no harmful effect on normal hematopoiesis. It inhibits the constitutive activation of STAT-3 DNA binding and IL-2-induced growth of MF tumor cells. It displays apoptotic and antiproliferative properties with IC50 of 1.7, 2.8 and 6.1 µM in 2E8, Baf/3 and Jurkat cells, respectively. [1][2]

References:

[1] J Immunol 1999;162;3897-3904

[2] Nature 1996;379:645-648

Chemical Information

Molecular Weight (WM): 294.30
Formula:

C17H14N2O3

Solubility(R.T.:25°C): DMSO 59mg/mL 
Water <1mg/mL 
Ethanol 6mg/mL 

Quality Control

View current batch:
H-NMR HPLC H-NMR HPLC

Research Area

Recommended Screening Libraries

Related Inhibitors

Related Antibodies

AG-490 has been referenced in 2 publications.

The Activity of the Androgen Receptor Variant AR-V7 Is Regulated by FOXO1 in a PTEN-PI3K-AKT-Dependent Way
RANKL downregulates cell surface CXCR6 expression through JAK2/STAT3 signaling pathway during osteoclastogenesis.

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