tcsc1822 Gimeracil

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Product Description

Gimeracil(Gimestat) is an inhibitor of dihydropyrimidine dehydrogenase (DPYD), which degrades pyrimidine including 5-fluorouracil in the blood; inhibits homologous recombination.

IC50 Value:

Target: DPYD

in vitro: Gimeracil had radiosensitizing effects by partially inhibiting homologous recombination (HR) in the repair of DNA double strand breaks. Tail moments in neutral comet assay increased in gimeracil-treated cells. Gimeracil restrained the formation of foci of Rad51 and replication protein A (RPA), whereas it increased the number of foci of Nbs1, Mre11, Rad50, and FancD2. Gimeracil did not sensitize DPYD-depleted cells [1]. Gimeracil inhibited DNA DSB repair. It did not sensitize cells deficient in HR but sensitized those deficient in NHEJ. In SCneo assay, Gimeracil reduced the frequency of neo-positive clones. Additionally, it sensitized the cells in S-phase more than in G0/G1 [2].

in vivo:

Information

CAS No103766-25-2
FormulaC5H4ClNO2
Clinical Informationclinicalinformation
PathwayOthers
TargetOthers

Specifications

Purity / Grade>98%
SolubilityDMSO : 29 mg/mL (199.26 mM; Need ultrasonic and warming)
Smilessmiles

Misc Information

Alternative NamesGimestat
Observed Molecular Weight145.54
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