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Gimeracil

Catalog No. T0987Cas No. 103766-25-2
Alias Gimestat

Gimeracil (Gimestat) is a competitive, reversible inhibitor of dihydropyrimidine dehydrogenase.

Gimeracil

Gimeracil

Purity: 99.86%
Catalog No. T0987Alias GimestatCas No. 103766-25-2
Gimeracil (Gimestat) is a competitive, reversible inhibitor of dihydropyrimidine dehydrogenase.
Pack SizePriceAvailabilityQuantity
25 mg$51In Stock
50 mg$68In Stock
100 mg$90In Stock
200 mg$110In Stock
500 mg$131In Stock
1 mL x 10 mM (in DMSO)$54In Stock
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Purity:99.86%
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Product Introduction

Bioactivity
Description
Gimeracil (Gimestat) is a competitive, reversible inhibitor of dihydropyrimidine dehydrogenase.
Kinase Assay
Microdilution method: The culture media used are RPMI 1640 with glutamine, without bicarbonate and phenol red, buffered with morpholinopropanesulfonic acid (MOPS) (0.165 M, pH 7.0). Two-fold serial dilutions of Flucytosine (0.06-64 μg/mL) are prepared and dispensed in 50 uL aliquot, in flat-bottom 96-well assay plates which are kept frozen at -70 °C in sealed plastic bags until used. The inoculum is prepared spectrophotometrically and standardized to a concentration of 1.0-5.0 × 103 cfu per mL. A 50 μL volume of this suspension is used to inoculate each well containing 50 μL of the double concentration of Flucytosine to be tested. Once inoculated, each well therefore contains 100 μL of broth favoured over 200 μL to facilitate the agitation of the plates prior to spectrophotometric reading. After an incubation period of 24 and 48 hours at 35 °C, the plates are agitated for 3 minutes at 900 r.p.m. with a shaker and the optical density of the growth in each well is determined with the use of an automatic plate reader set at 495 nm. The inhibitory concentration of IC50 is computed mathematically.
AliasGimestat
Chemical Properties
Molecular Weight145.54
FormulaC5H4ClNO2
Cas No.103766-25-2
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
Ethanol: < 1 mg/mL (insoluble or slightly soluble)
H2O: < 1 mg/mL (insoluble or slightly soluble)
DMSO: 35 mg/mL (240.48 mM)
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM6.8710 mL34.3548 mL68.7096 mL343.5482 mL
5 mM1.3742 mL6.8710 mL13.7419 mL68.7096 mL
10 mM0.6871 mL3.4355 mL6.8710 mL34.3548 mL
20 mM0.3435 mL1.7177 mL3.4355 mL17.1774 mL
50 mM0.1374 mL0.6871 mL1.3742 mL6.8710 mL
100 mM0.0687 mL0.3435 mL0.6871 mL3.4355 mL

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Please enter your animal experiment information in the following box and click Calculate to obtain the mother liquor preparation method and in vivo formula preparation method:
TargetMol | Animal experimentsFor example, your dosage is 10 mg/kg Each animal weighs 20 g, and the dosage volume is 100 μL . TargetMol | Animal experiments A total of 10 animals were administered, and the formula you used is 5% TargetMol | reagent DMSO+30% PEG300+5% Tween 80+60% ddH2O. So your working solution concentration is 2 mg/mL。
Mother liquor preparation method: 2 mg of drug dissolved in 50 μL DMSOTargetMol | reagent (mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.
Preparation method for in vivo formula: Take 50 μL DMSOTargetMol | reagent main solution, add 300 μLPEG300TargetMol | reagent mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2OTargetMol | reagent mix well and clarify
For Reference Only. Please develop an appropriate dissolution method based on your laboratory animals and route of administration.
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