Merck
  • F0503
All Photos(4)

F0503

Sigma-Aldrich

5-Fluoro-2′-deoxyuridine

thymidylate synthase inhibitor

Synonym(s):
floxuridine, 2′-Deoxy-5-fluorouridine, FUDR, Floxuridine
Empirical Formula (Hill Notation):
C9H11FN2O5
CAS Number:
Molecular Weight:
246.19
Beilstein:
90221
Numer EC:
Numer MDL:
Identyfikator substancji w PubChem:
NACRES:
NA.77

pochodzenie biologiczne

synthetic (organic)

Poziom jakości

próba

≥99% (HPLC)

forma

powder

mp

148 °C (lit.)

rozpuszczalność

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

temp. przechowywania

room temp

SMILES string

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

InChI key

ODKNJVUHOIMIIZ-RRKCRQDMSA-N

Gene Information

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

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1 of 4

This Item
F8791PHR2850F5307
5′-deoxy-5-fluorouridine certified reference material, pharmaceutical secondary standard

Supelco

PHR2850

5′-deoxy-5-fluorouridine

biological source

synthetic (organic)

biological source

-

biological source

-

biological source

-

assay

≥99% (HPLC)

assay

-

assay

-

assay

≥98% (HPLC)

form

powder

form

-

form

solid

form

powder

mp

148 °C (lit.)

mp

-

mp

-

mp

-

solubility

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

solubility

-

solubility

-

solubility

DMSO: >20 mg/mL

storage temp.

room temp

storage temp.

-

storage temp.

2-30°C

storage temp.

room temp

Opis ogólny

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.

Zastosowanie

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.

Działania biochem./fizjol.

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.

piktogramy

Skull and crossbones

Hasło ostrzegawcze

Danger

Zwroty wskazujące rodzaj zagrożenia

Zwroty wskazujące środki ostrożności

Klasyfikacja zagrożeń

Acute Tox. 3 Oral

Kod klasy składowania

6.1D - Non-combustible, acute toxic Cat.3 / toxic hazardous materials or hazardous materials causing chronic effects

WGK

WGK 3

Temperatura zapłonu °F

Not applicable

Temperatura zapłonu °C

Not applicable

Środki ochrony indywidualnej

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

Certificate of Analysis

Enter Lot Number to search for Certificate of Analysis (COA).

Certificate of Origin

Enter Lot Number to search for Certificate of Origin (COO).

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