ChemicalBook--->CAS DataBase List--->122520-85-8

122520-85-8

122520-85-8 Structure

122520-85-8 Structure
IdentificationBack Directory
[Name]

AG 99
[CAS]

122520-85-8
[Synonyms]

AG 99
(E)-AG 99
TYRPHOSTIN 46
TYRPHOSTIN A46
TYRPHOSTIN B40
AG 99 USP/EP/BP
TYRPHOSTIN AG 99
(E)-Tyrphostin 46
TYRPHOSTIN A46 99%
(E)-Tyrphostin AG 99
3,4-DIHYDROXY-ALPHA-CYANOCINNAMIDE
ALPHA-CYANO-(3,4-DIHYDROXY)CINNAMIDE
(E)-2-Cyano-3-(3,4-dihydroxyphenyl)acrylamide
2-cyano-3-(3,4-dihydroxyphenyl)prop-2-enamide
(E)-2-Cyano-3-(3,4-dihydroxyphenyl)propenamide
(E)-2-CYANO-3-(3,4-DIHYDROXYPHENYL)-2-PROPENAMIDE
2-Propenamide, 2-cyano-3-(3,4-dihydroxyphenyl)-, (2E)-
2-Propenamide, 2-cyano-3-(3,4-dihydroxyphenyl)-, (2E)- (9CI)
[Molecular Formula]

C10H8N2O3
[MDL Number]

MFCD00133901
[MOL File]

122520-85-8.mol
[Molecular Weight]

204.18
Chemical PropertiesBack Directory
[Melting point ]

247 °C
[Boiling point ]

544.4±50.0 °C(Predicted)
[density ]

1.482±0.06 g/cm3(Predicted)
[storage temp. ]

Inert atmosphere,Room Temperature
[solubility ]

Soluble in DMSO
[form ]

Brown solid.
[pka]

8.81±0.10(Predicted)
[color ]

Light yellow to yellow
[InChI]

InChI=1S/C10H8N2O3/c11-5-7(10(12)15)3-6-1-2-8(13)9(14)4-6/h1-4,13-14H,(H2,12,15)/b7-3+
[InChIKey]

USOXQZNJFMKTKJ-XVNBXDOJSA-N
[SMILES]

C(N)(=O)/C(/C#N)=C/C1=CC=C(O)C(O)=C1
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
Hazard InformationBack Directory
[Uses]

Tyrphostin AG 99 is a potent, cell-permeable and reversible inhibitor of EGFR and EGF-dependent cell proliferation.
[Biological Activity]

Epidermal growth factor receptor (EGFR) kinase inhibitor (IC 50 = 10 μ M) that is selective over insulin receptor kinase. Blocks tyrosine phosphorylation of p145 met and promotes cell death of normal and cancer cells via activation of caspase-like proteases in vitro .
[IC 50]

EGFR
[References]

[1]. gazit a, osherov n, gilon c, et al. tyrphostins. 6. dimeric benzylidenemalononitrile tyrophostins: potent inhibitors of egf receptor tyrosine kinase in vitro. j med chem, 1996, 39(25): 4905-4911.
[2]. yamamoto n, mammadova g, song rx, et al. tyrosine phosphorylation of p145met mediated by egfr and src is required for serum-independent survival of human bladder carcinoma cells. j cell sci, 2006, 119(pt 22): 4623-4633.
Spectrum DetailBack Directory
[Spectrum Detail]

AG 99(122520-85-8)1HNMR
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