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AG 1478 hydrochloride

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Category Hepatitis C Virus (HCV)
CAS 170449-18-0
Description The hydrochloride salt form of AG 1478, which has been found to be an epidermal growth factor receptor tyrosine kinase inhibitor.
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Product Information

Synonyms AG 1478 hydrochloride; AG1478 hydrochloride; AG-1478 hydrochloride; N-(3-Chlorophenyl)-6,7-dimethoxy-4-quinazolinanine hydrochloride
Molecular Weight 352.22
Molecular Formula C16H14ClN3O2.HCl
Canonical SMILES COC1=C(C=C2C(=C1)C(=NC=N2)NC3=CC(=CC=C3)Cl)OC.Cl
InChI InChI=1S/C16H14ClN3O2.ClH/c1-21-14-7-12-13(8-15(14)22-2)18-9-19-16(12)20-11-5-3-4-10(17)6-11;/h3-9H,1-2H3,(H,18,19,20);1H
InChIKey WDJDYIUSDDVWKB-UHFFFAOYSA-N
Boiling Point 458.5ºC at 760mmHg
Flash Point 231.1ºC
Purity ≥98% by HPLC
Density 1.337g/cm3
Solubility DMSO: Soluble
Appearance Cream Solid
Storage Store at -20°C
Exact Mass 351.054138
In Vitro AG-1478 is irreversible for growth regulation of human lung (A549) and prostate (DU145) cancer cell lines. AG-1478 seems to be more effective at lower concentrations, but is unable to completely inhibit growth of A549 cells. Inhibition of EGFR by specific tyrosine kinase inhibitor AG-1478 significantly decreases the angiotensin II-mediated synthesis of TGF-β and fibronectin by cardiac fibroblasts. EGFR is pharmacologically inhibited by small-molecule inhibitor AG-1478 with IC50 of 4 nM.
In Vivo Administration of AG-1478 significantly reduces myocardial inflammation, fibrosis, Apoptosis, and dysfunction in both two obese mouse models.
PSA 56.27000
Target EGFR: 3 nM(IC50); HCV; EMCV
Vapor Pressure 1.37E-08mmHg at 25°C

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