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126433-07-6

126433-07-6 Structure

126433-07-6 Structure
IdentificationBack Directory
[Name]

TYRPHOSTIN A51
[CAS]

126433-07-6
[Synonyms]

AG 183
Aids086066
Aids-086066
TYRPHOSTIN 51
TYRPHOSTIN A51
TYRPHOSTIN AG 183
Tyrphostin 51 >=98%
2-AMINO-1,1,3-TRICYANO-4-[3',4',5'-TRIHYDROXYPHENYL]BUTADIENE
2-AMINO-4-(3',4',5'-TRIHYDROXYPHENYL)-1,1,3-TRICYANOBUTA-1,3-DIENE
3-AMINO-2,4-DICYANO-5-(3',4',5'-TRIHYDROXYPHENYL)PENTA-2,4-DIENONITRILE
1,3-Butadiene-1,1,3-tricarbonitrile, 2-amino-4-(3,4,5-trihydroxyphenyl)-
[Molecular Formula]

C13H8N4O3
[MDL Number]

MFCD00133903
[MOL File]

126433-07-6.mol
[Molecular Weight]

268.23
Chemical PropertiesBack Directory
[Boiling point ]

788.2±60.0 °C(Predicted)
[density ]

1.591±0.06 g/cm3(Predicted)
[storage temp. ]

2-8°C
[solubility ]

DMSO: soluble5 mg of Tyrphostin 51 in 0.1 ml of solvent, clear, orange to red
[form ]

Solid
[pka]

8.27±0.15(Predicted)
[color ]

White to yellow
Safety DataBack Directory
[WGK Germany ]

3
Hazard InformationBack Directory
[Uses]

Tyrphostin 51 has been used to study the inhibition of rat hepatic leptin 1.
[Definition]

ChEBI: 2-amino-4-(3,4,5-trihydroxyphenyl)buta-1,3-diene-1,1,3-tricarbonitrile is a benzenetriol.
[Biochem/physiol Actions]

Tyrphostin 51 is a small molecule inhibitor of epidermal growth factor (EGF) receptor kinase function. This molecule associates with the substrate subsite of the protein tyrosine kinase (PTK) domain,.
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