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5-Fluoro-2′-deoxyuridine

≥98% (HPLC), solid, thymidylate synthase inhibitor, Calbiochem®

Synonym(s):

5-Fluoro-2′-deoxyuridine, FdUrd, FUdR, 5-FdU, Floxuridine

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About This Item

Empirical Formula (Hill Notation):
C9H11FN2O5
CAS Number:
Molecular Weight:
246.19
UNSPSC Code:
12352200
NACRES:
NA.77
MDL number:
Assay:
≥98% (HPLC)
Form:
solid
Storage condition:
OK to freeze
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Product Name

5-Fluoro-2′-deoxyuridine, Experimental anticancer agent shown to have activity against a variety of malignant neoplasms, including mouse mammary tumors and colorectal carcinomas.

Quality Segment

description

Merck USA index - 14, 4112

assay

≥98% (HPLC)

form

solid

manufacturer/tradename

Calbiochem®

storage condition

OK to freeze

color

white

solubility

aqueous buffer: 1 mg/mL, water: 1 mg/mL

shipped in

ambient

storage temp.

2-8°C

SMILES string

Fc1[c]([nH][c]([n](c1)[C@@H]2O[C@@H]([C@H](C2)O)CO)=O)=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

General description

Experimental anti-cancer agent shown to have activity against a variety of malignant neoplasms, including mouse mammary tumors and colorectal carcinomas.
Experimental anticancer agent shown to have activity against a variety of malignant neoplasms, including mouse mammary tumors and colorectal carcinomas.

Biochem/physiol Actions

Cell permeable: no
Primary Target
Experimental anticancer agent
Product does not compete with ATP.
Reversible: no

Other Notes

Due to the nature of the Hazardous Materials in this shipment, additional shipping charges may be applied to your order. Certain sizes may be exempt from the additional hazardous materials shipping charges. Please contact your local sales office for more information regarding these charges.
Nakagama, H., et al. 2001. Jpn. J. Clin. Oncol.31, 251.
Malmberg, M., et al. 1993. Cell Prolif. 26, 291.

Legal Information

CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany

Disclaimer

Toxicity: Toxic & Carcinogenic / Teratogenic (G)

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This Item
PHR2589F05031271008
description

Experimental anticancer agent shown to have activity against a variety of malignant neoplasms, including mouse mammary tumors and colorectal carcinomas.

description

pharmaceutical secondary standard, certified reference material

description

thymidylate synthase inhibitor

description

United States Pharmacopeia (USP) Reference Standard

assay

≥98% (HPLC)

assay

-

assay

≥99% (HPLC)

assay

-

form

solid

form

powder

form

powder

form

-

Quality Level

100

Quality Level

300

Quality Level

200

Quality Level

-

manufacturer/tradename

Calbiochem®

manufacturer/tradename

-

manufacturer/tradename

-

manufacturer/tradename

USP

storage temp.

2-8°C

storage temp.

2-30°C

storage temp.

room temp

storage temp.

-

solubility

water: 1 mg/mL, aqueous buffer: 1 mg/mL

solubility

-

solubility

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

solubility

-


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Pictograms

Skull and crossbones

Signal Word

Danger

Hazard Codes

Hazard Classifications

Acute Tox. 3 Oral

Storage Class

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

WGK

WGK 3



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