5-Fluoro - 2 - déoxyuridine, inhibiteur de synthase thymidylate

Code: f0503-1g D2-231

Non disponible en dehors du Royaume-Uni et de l'Irlande

Application

5-Fluoro-2′-deoxyuridine has been used as a mitotic inhibitor in schwann cell proliferation, glia proliferation and nonneuronal cells in dorsal root ganglion cult...


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Votre prix
$1,307.90 1G
$1,569.48 inc. VAT

Non disponible en dehors du Royaume-Uni et de l'Irlande

Application

5-Fluoro-2′-deoxyuridine has been used as a mitotic inhibitor in schwann cell proliferation, glia proliferation and nonneuronal cells in dorsal root ganglion cultures.

Biochem/physiol Actions

Antineoplastic drug that acts as a potent inhibitor of thymidylate synthetase Resistance to FUdR can develop in cancer cell cultures, among other means, by low-level Mycoplasma infection.

General description

5-Fluoro-2′-deoxyuridine, also called floxuridine elicits DNA-directed cytotoxicity in cancer cells. Floxuridine is effective for treating liver cancer and eliminating virulence of Staphylococcus aureus. Dipeptide prodrugs combination of floxuridine with gemcitabine are more cell permeable and display enhanced anti-proliferative activity. Floxuridine is effective on solid tumours and advanced stage cancers.

Packaging

1 g in poly bottle

100, 250 mg in poly bottle

assay≥99% (HPLC)
biological sourcesynthetic (organic)
formpowder
Gene Informationhuman ... TYMS(7298)mouse ... Tyms(22171)
InChI keyODKNJVUHOIMIIZ-RRKCRQDMSA-N
InChI1S/C9H11FN2O5/c10-4-2-12(9(16)11-8(4)15)7-1-5(14)6(3-13)17-7/h2,5-7,13-14H,1,3H2,(H,11,15,16)/t5-,6+,7+/m0/s1
mp148 °C (lit.)
Quality Level200
SMILES stringOC[C@H]1O[C@H](C[C@@H]1O)N2C=C(F)C(=O)NC2=O
solubilitywater: 50 mg/mL, clear, colorless to faintly yellow
storage temp.room temp
Code
Description
Unité de vente
Prix annoncé
Qté
F0503-100MG
Unité:100MG
Prix annoncé: $256.65
Source:Prix annoncé
F0503-250MG
Unité:250MG
Prix annoncé: $584.35
Source:Prix annoncé
Cas Number50-91-9
Hazard Class6.1
Un Number2811
Pack GroupIII
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