AG 213

AG 213
  • CAS No.:122520-86-9
Other grades of this product :
AG 213 Basic information
Product Name:AG 213
Synonyms:ALPHA-CYANO-3,4-DIHYDROXYTHIOCINNAMAMIDE;ALPHA-CYANO-(3,4-DIHYDROXY)THIOCINNAMIDE;AG 213;3,4-DIHYDROXY-ALPHA-CYANOTHIOCINNAMAMIDE;(E)-2-CYANO-3-(3,4-DIHYDROXYPHENYL)-2-PROPENTHIOAMIDE;TYRPHOSTIN A47 99+%;AG 213 (Tyrphostin AG 213);ZGHQGWOETPXKLY-XVNBXDOJSA-N
CAS:122520-86-9
MF:C10H8N2O2S
MW:220.25
EINECS:
Product Categories:Intracellular Signaling;Protein Kinase
Mol File:122520-86-9.mol
AG 213 Chemical Properties
storage temp. 2-8°C
solubility DMSO: 50 mg/mL, clear, orange
form Orange solid.
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36
WGK Germany 3
10
MSDS Information
ProviderLanguage
SigmaAldrich English
AG 213 Usage And Synthesis
DescriptionProtein tyrosine kinase (PTK) inhibitors are potential antiproliferative agents for diseases caused by the hyperactivity of PTKs. Tyrphostins are a class of antiproliferative compounds that act as PTK blockers. PTK inhibitors which preferentially inhibit the epidermal growth factor (EGF) receptor kinase block EGF-dependent cell proliferation. AG-213 is an inhibitor of epidermal growth factor (EGF) receptor kinase with an IC50 value of 2.4 μM in the human epidermoid carcinoma cell line A431.
UsesTyrphostin 47 is a potent inhibitor of EGFR kinase activity.
Biological ActivityEpidermal growth factor receptor (EGFR) and platelet-derived growth factor receptor (PDGFR) kinase inhibitor (IC 50 values are 2.4 and 3 μ M respectively). Stimulates microtubule polymerization and promotes neurite outgrowth > 17-fold over basal conditions in vitro . Also weakly inhibits protein kinase C (IC 50 = 60 μ M).
references[1] romer l h, mclean n, turner c e, et al. tyrosine kinase activity, cytoskeletal organization, and motility in human vascular endothelial cells[j]. molecular biology of the cell, 1994, 5(3): 349-361.[2] gazit a, yaish p, gilon c, et al. tyrphostins i: synthesis and biological activity of protein tyrosine kinase inhibitors[j]. journal of medicinal chemistry, 1989, 32(10): 2344-2352.[3] levitzki a, gazit a. tyrosine kinase inhibition: an approach to drug development[j]. science, 1995, 267(5205): 1782.[4] herbst r s. review of epidermal growth factor receptor biology[j]. international journal of radiation oncology biology physics, 2004, 59(2): s21-s26.
AG 213 Preparation Products And Raw materials

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