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Results for "

DPDS (Standard)

" in MedChemExpress (MCE) Product Catalog:

4

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Products

Cat. No. Product Name Target Research Areas Chemical Structure
  • HY-W196803R

    Propyl Disulfide (Standard); DPDS (Standard)

    Cytochrome P450 Reference Standards Others
    Dipropyl disulfide is oxidized to dipropyl thiosulfinate (DPDSO) by rat microsomes. Both flavincontaining monooxygenases (FMO) and cytochrome P450 enzymes (CYPs) are involved in dipropyl disulfide oxidation. Dipropyl disulfide forms two metabolites: propylglutathione sulfide conjugate and propylthiol .
    Dipropyl disulfide (Standard)
  • HY-W012926R

    5,6-Dihydrouracil (Standard)

    Reference Standards Endogenous Metabolite Metabolic Disease
    Dihydrouracil (Standard) is the analytical standard of Dihydrouracil. This product is intended for research and analytical applications. Dihydrouracil (5,6-Dihydrouracil), a metabolite of Uracil, can be used as a marker for identification of dihydropyrimidine dehydrogenase (DPD)-deficient[1][2].
    Dihydrouracil (Standard)
  • HY-17469R

    Gimestat (Standard)

    DNA/RNA Synthesis Dihydropyrimidine Dehydrogenase (DPD) Reference Standards Cancer
    Gimeracil (Standard) is the analytical standard of Gimeracil. This product is intended for research and analytical applications. Gimeracil, a component of an oral fluoropyrimidine derivative S-1, inhibits DNA DSB repair and is a potent inhibitor of DPYD (dihydropyrimidine dehydrogenase, DPD) .
    Gimeracil (Standard)
  • HY-10533R

    5-Ethynyluracil (Standard); GW776C85 (Standard)

    Biochemical Assay Reagents Reference Standards Cancer
    Eniluracil (Standard) is the analytical standard of Eniluracil. This product is intended for research and analytical applications. Eniluracil (5-Ethynyluracil) is an orally active dihydropyrimidine dehydrogenase (DPD) inhibitor. Eniluracil irreversibly inhibits DPD, increases the oral bioavailability of 5-fluorouracil to 100%, and facilitates the uniform absorption and toxicity of 5-fluorouracil. Eniluracil can be used in cancer research of combination with fluoropyrimidines (including 5-fluorouracil) . Eniluracil is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
    Eniluracil (Standard)

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