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F0503

Sigma-Aldrich

5-Fluoro-2′-deoxyuridine

thymidylate synthase inhibitor

Sinonimo/i:

floxuridine, 2′-Deoxy-5-fluorouridine, FUDR, Floxuridine

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100 MG
CHF 341.00
250 MG
CHF 771.00
1 G
CHF 1’960.00

CHF 341.00


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Cambia visualizzazione
100 MG
CHF 341.00
250 MG
CHF 771.00
1 G
CHF 1’960.00

About This Item

Formula empirica (notazione di Hill):
C9H11FN2O5
Numero CAS:
Peso molecolare:
246.19
Beilstein:
90221
Numero CE:
Numero MDL:
Codice UNSPSC:
12352202
ID PubChem:
NACRES:
NA.77

CHF 341.00


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Origine biologica

synthetic (organic)

Saggio

≥99% (HPLC)

Stato

powder

Punto di fusione

148 °C (lit.)

Solubilità

water: 50 mg/mL, clear, colorless to faintly yellow

Temperatura di conservazione

room temp

Stringa SMILE

OC[C@H]1O[C@H](C[C@@H]1O)N2C=C(F)C(=O)NC2=O

InChI

1S/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
ODKNJVUHOIMIIZ-RRKCRQDMSA-N

Informazioni sul gene

human ... TYMS(7298)
mouse ... Tyms(22171)

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Descrizione generale

5-Fluoro-2′-deoxyuridine, also called floxuridine elicits DNA-directed cytotoxicity in cancer cells.[1] Floxuridine is effective for treating liver cancer[2] and eliminating virulence of Staphylococcus aureus.[3] Dipeptide prodrugs combination of floxuridine with gemcitabine are more cell permeable and display enhanced anti-proliferative activity.[4] Floxuridine is effective on solid tumours and advanced stage cancers.[5]

Applicazioni

5-Fluoro-2′-deoxyuridine has been used as a mitotic inhibitor in schwann cell proliferation[6], glia proliferation[7][8] and nonneuronal cells in dorsal root ganglion cultures.[9]

Azioni biochim/fisiol

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.

Pittogrammi

Skull and crossbones

Avvertenze

Danger

Indicazioni di pericolo

Consigli di prudenza

Classi di pericolo

Acute Tox. 3 Oral

Codice della classe di stoccaggio

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

dust mask type N95 (US), Eyeshields, Faceshields, Gloves


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The Dipeptide Monoester Prodrugs of Floxuridine and Gemcitabine?Feasibility of Orally Administrable Nucleoside Analogs
Tsume Y, et al.
Pharmaceuticals (Basel, Switzerland), 7(2), 169-191 (2014)
J A van Laar et al.
European journal of cancer (Oxford, England : 1990), 34(3), 296-306 (1998-06-26)
Despite more than 30 years of intensive studies on new drugs against advanced colorectal cancer, the fluoropyrimidines remain the drugs of choice for systemic treatment and for hepatic artery infusion (HAI). This overview describes new developments in advanced colorectal cancer
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Questions

  1. Is it possible to sterile filter (0.2 mikrometer) this compound for safer use in cell culture?

    1 answer
    1. This product is soluble in water at 50 mg/mL. Solutions may be filter sterilized and are stable for 2 weeks at 2-8 °C. Solutions should be protected from light.
      See the link below to review the product datasheet:
      https://www.sigmaaldrich.com/deepweb/assets/sigmaaldrich/product/documents/716/505/f0503pis.pdf

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