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AG 555

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Category Influenza Virus
CAS 133550-34-2
Description AG 555 is an epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor (IC50 = 0.7 μM) with 50-fold and >140-fold selectivity over ErbB2 and insulin receptor kinase respectively.
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Product Information

Synonyms AG 555; AG-555; AG555; (E)-2-cyano-3-(3,4-dihydroxyphenyl)-N-(3-phenylpropyl)prop-2-enamide; AG 555; AG-555; alpha-cyano-(3,4-dihydroxy)-N-(3-phenylpropyl)cinnamide; N-(3'-Phenylpropyl)-3,4-dihydroxybenzylidenecyanoacetamide; N-(3-phenylpropyl)-3,4-dihydroxybenzylidene cyanoacetamide; tyrphostin AG 555; tyrphostin AG-555; tyrphostin B46
IUPAC Name (E)-2-cyano-3-(3,4-dihydroxyphenyl)-N-(3-phenylpropyl)prop-2-enamide
Molecular Weight 322.36
Molecular Formula C19H18N2O3
Canonical SMILES C1=CC=C(C=C1)CCCNC(=O)C(=CC2=CC(=C(C=C2)O)O)C#N
InChI 1S/C19H18N2O3/c20-13-16(11-15-8-9-17(22)18(23)12-15)19(24)21-10-4-7-14-5-2-1-3-6-14/h1-3,5-6,8-9,11-12,22-23H,4,7,10H2,(H,21,24)/b16-11+
InChIKey GSQOBTOAOGXIFL-LFIBNONCSA-N
Boiling Point 621.1±55.0 ℃ at 760 Torr
Flash Point 329.4±31.5 °C
Purity ≥98% (HPLC)
Density 1.273±0.06 g/cm3
Solubility DMSO
Appearance Light yellow to yellow (Solid)
Storage Store in a cool and dry place (or refer to the Certificate of Analysis).
Complexity 488
Exact Mass 322.131744
Index Of Refraction 1.650
In Vitro AG 555 inhibits both the early stages (integration process) and the late stages (viral protein synthesis) in the virus life cycle. Tyrphostins AG555, which blocks Cdk2 activation, induces growth arrest of immortalized cells at G1-S and early S and is very effective in arresting the growth of EGFR overexpressor cells. Tyrphostin AG 555 can selectively suppress BPV-1 transcription through MAP kinase pathway activation and binding of phosphorylated JuTF-2 at a novel intragenic regulatory sequence.
Target EGFR; Reverse Transcriptase
Vapor Pressure 0.0±1.9 mmHg at 25°C
XLogP3-AA 3.2

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