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ChemicalBook--->CAS DataBase List--->192718-06-2

192718-06-2

192718-06-2 Structure

192718-06-2 Structure
IdentificationBack Directory
[Name]

2-(4-Fluorophenyl)naphtho[2,3-d]oxazole-4,9-dione
[CAS]

192718-06-2
[Synonyms]

C527
C527 >=98% (HPLC)
2-(4-Fluorophenyl)naphtho[2,3-d]oxazole-4,9-dione
2-(4-Fluorophenyl)-naphth[2,3-d]oxazole-4,9-dione
Naphth[2,3-d]oxazole-4,9-dione, 2-(4-fluorophenyl)-
[Molecular Formula]

C17H8FNO3
[MDL Number]

MFCD01033540
[MOL File]

192718-06-2.mol
[Molecular Weight]

293.25
Chemical PropertiesBack Directory
[Boiling point ]

488.6±47.0 °C(Predicted)
[density ]

1.433±0.06 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[solubility ]

DMSO: soluble0.3mg/mL, clear (warmed)
[form ]

powder
[pka]

-4.21±0.20(Predicted)
[color ]

faint yellow to dark yellow
Safety DataBack Directory
[Hazard Codes ]

Xn
[Risk Statements ]

22
[Safety Statements ]

46
[WGK Germany ]

3
Spectrum DetailBack Directory
[Spectrum Detail]

2-(4-Fluorophenyl)naphtho[2,3-d]oxazole-4,9-dione(192718-06-2)1HNMR
Hazard InformationBack Directory
[Biological Activity]

C527 is a pan-DUB enzyme inhibitor with high activity against USP1/UAF1 complex with IC50 value of 0.88 μM.
[in vitro]

Pretreatment of USP1/UAF1 with C527 resulted in inhibition of its enzyme activity with an IC 50 of 0.88±0.03 μM. C527 inhibits the DUB activity of the USP12/USP46 complex and other DUB enzymes in vitro . However, the IC 50 of C527 for these DUB enzymes was higher in comparison with USP1/UAF1 complex. C527 has considerably less inhibitory effect on UCH-L1 and UCH-L3, a different subclass of DUB enzymes. C527 treatments causes an increase in the levels of Ub-FANCD2 and Ub-FANCI. Pretreatment of cells with the C527 causes an enhancement in the cytoxicity of mitomycin C and camptothecin. C527 treatments lead to an increase in ubiquitinated forms of FANCD2 and FANCI, cause a decrease in homologous recombination activity, and sensitize cells to DNA damaging agents.

[target]

0.88 μM (USP1)

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