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ChemicalBook--->CAS DataBase List--->194423-15-9

194423-15-9

194423-15-9 Structure

194423-15-9 Structure
IdentificationBack Directory
[Name]

4-[(3-BROMOPHENYL)AMINO]-6-ACRYLAMIDOQUINAZOLINE
[CAS]

194423-15-9
[Synonyms]

CS-2316
PD 168393
PD168393 USP/EP/BP
PD-168393;PD 168393
PD168393;PD-168393;PD 168393
4-[(3-BROMOPHENYL)AMINO]-6-ACRYLAMIDOQUINAZOLINE
N-[4-(3-Bromoanilino)quinazolin-6-yl]prop-2-enamide
N-(4-((3-Bromophenyl)amino)quinazolin-6-yl)acrylamide
N-[4-[(3-Bromophenyl)amino]-6-quinazolinyl]-2-propenamide
2-Propenamide, N-[4-[(3-bromophenyl)amino]-6-quinazolinyl]-
[Molecular Formula]

C17H13BrN4O
[MDL Number]

MFCD02179207
[MOL File]

194423-15-9.mol
[Molecular Weight]

369.22
Chemical PropertiesBack Directory
[Melting point ]

279℃
[storage temp. ]

-20°C
[solubility ]

insoluble in H2O; ≥1 mg/mL in EtOH with gentle warming and ultrasonic; ≥18.45 mg/mL in DMSO
[form ]

powder
[color ]

white to beige
Hazard InformationBack Directory
[Uses]

Potent, cell permeable, irreversible, and selective inhibitor of EGF receptor (EGFR) tyrosine kinase activity (IC50=700pM). Antitumor agent in vivo.
[Definition]

ChEBI: A member of the class of quinazolines carrying bromoanilino and acrylamido substituents at positions 4 and 6 respectively.
[Biochem/physiol Actions]

PD168393 is a 6-acrylamido-4-anilinoquinazoline compound. It increases apoptosis in malignant peripheral nerve sheath tumor cells, stimulated by lysosomal dysfunction.
[Enzyme inhibitor]

This photosensitive quinazoline (FW = 369.22 g/mol), also known as 4-[ (3- bromophenyl) amino]-6-acrylamido-quinazoline, irreversibly inhibits epidermal growth factor receptor (EGFR) protein-tyrosine kinase, IC50 = 0.7 nM. See also PD 174265
[target]

EGFR
Spectrum DetailBack Directory
[Spectrum Detail]

PD168393(194423-15-9)1HNMR
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