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PD168393
Cat. No.:
OB0225WX-2663
Appearance:
Solid
Purity:
≥99%
Identity:
Confirmed by NMR, and HPLC.
Size:
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Product Overview
Description:
PD168393 functions as an irreversible antagonist of EGFR (IC50: 0.70 nM) by covalently alkylating the Cys-773 residue, while remaining inactive against PKC, FGFR, PDGFR, and insulin receptors.
Synonym:
194423-15-9; PD-168393; 4-[(3-Bromophenyl)amino]-6-acrylamidoquinazoline; pd 168393; N-(4-((3-bromophenyl)amino)quinazolin-6-yl)acrylamide; n-{4-[(3-bromophenyl)amino]quinazolin-6-yl}prop-2-enamide; N-[4-(3-bromoanilino)quinazolin-6-yl]prop-2-enamide; 2-Propenamide, N-(4-((3-bromophenyl)amino)-6-quinazolinyl)-; nchembio866-comp2; N-[4-[(3-bromophenyl)amino]quinazolin-6-yl]acrylamide; 4-anilinoquinazoline deriv. 2; N-(4-(3-Bromophenylamino)quinazolin-6-yl)acrylamide; N-{4-[(3-bromophenyl)amino]quinazolin-6-yl}prop-2-enamide;4-[(3-Bromophenyl)amino]-6-acrylamidoquinazoline
CAS No.:
194423-15-9
Compound CID:
4708
Formula:
C17H13BrN4
Formula Weight:
369.22
Specification
Stability:
3 years in powder form.
Storage:
Storage at -20°C.
Applications:
PD168393 is utilized in oncology research as a potent and irreversible inhibitor of the EGFR tyrosine kinase to study the suppression of aberrant growth signaling in various solid tumor models.
Library Information
Target:
EGFR
Receptor:
EGFR
Pathways:
Protein tyrosine kinase
Plate Number:
L6700-08
Empty Location:
a1-h1; a12-h12
Container:
96-well plate
Formulation:
10mM DMSO
DMSO Max Solubility:
73 mg/mL; 197.71 mM
ALogP:
4.043
HBA_Count:
3
HBD_Count:
2
Rotatable Bond:
4





