ChemicalBook--->CAS DataBase List--->79756-69-7

79756-69-7

79756-69-7 Structure

79756-69-7 Structure
IdentificationBack Directory
[Name]

2-(2,5-dichlorophenyl)cyclohexa-2,5-diene-1,4-dione
[CAS]

79756-69-7
[Synonyms]

TPI-1
TPI1;TPI 1
2-(2,5-Dichlorophenyl)-1,4-benzoquinone
Recombinant Human TIM/TPI1 Protein, His Tag
2,5-Cyclohexadiene-1,4-dione, 2-(2,5-dichlorophenyl)-
[Molecular Formula]

C12H6Cl2O2
[MDL Number]

MFCD00448731
[MOL File]

79756-69-7.mol
[Molecular Weight]

253.08
Chemical PropertiesBack Directory
[storage temp. ]

Sealed in dry,2-8°C
[solubility ]

DMF: 30 mg/ml; DMSO: 30 mg/ml; Ethanol: 1 mg/ml
[form ]

A crystalline solid
[color ]

White to yellow
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[HS Code ]

2914698090
Spectrum DetailBack Directory
[Spectrum Detail]

2-(2,5-dichlorophenyl)cyclohexa-2,5-diene-1,4-dione(79756-69-7)1HNMR
Hazard InformationBack Directory
[Biological Activity]

TPI-1 (Tyrosine Phosphatase Inhibitor 1) is a potent SHP-1 inhibitor with IC50 of 40 nM for recombinant SHP-1. It has anticancer activity.
[in vitro]

SHP-1 has been implicated as a potential cancer therapeutic target. TPI-1 is effective starting at 10 ng/mL in increasing SHP-1 phospho-substrates pLck-pY394. It selectively increases SHP-1 phospho-substrates (pLck-pY394, pZap70 and pSlp76) in Jurkat T cells but has little effects on pERK1/2 or pLck-pY505. TPI-1 induces mouse splenic-IFNγ + cells and induces IFNγ < sup> + cells in human peripheral blood.

[in vivo]

TPI-1 inhibits the growth of B16 melanoma tumors in mice at a tolerated oral dose in a T cell-dependent manner but has little effects on B16 cell growth in culture. It thus also increases pLck-pY394 and IFNγ + cells in mice. TPI-1 also inhibits B16 tumor growth and prolongs tumor mice survival as a tolerated sc agent.

[target]

TargetValue
SHP-1
(Cell-free assay)
40 nM
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