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Tegafur

Manufactured by Tokyo Chemical Industry
Sourced in Japan

Tegafur is a laboratory chemical product manufactured by Tokyo Chemical Industry. It is a synthetic fluoropyrimidine compound used as a research tool in scientific investigations. The core function of Tegafur is to serve as a chemical reference standard or intermediate for research and development purposes. No additional interpretation or extrapolation on the intended use of this product is provided.

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3 protocols using tegafur

1

HPLC Analysis of Anti-Cancer Compounds

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Tegafur, 5-FU, gimeracil, and potassium oxonate were purchased from Tokyo Chemical Industry Co., Ltd. (Tokyo, Japan). SDT was obtained from Hankook Shinyak Corp. (Nonsan, Chungnam, Korea). Sodium carboxymethyl cellulose (CMC-Na) and methyl cellulose (MC) were obtained from Junsei Chemical (Tokyo, Japan). Acetonitrile and distilled water (all HPLC grades) were purchased from J.T. Baker, Inc. (Phillipsburg, NJ, USA), and formic acid was obtained from Aldrich Chemical Co. (Milwaukee, WI, USA).
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2

Quantification of 5-FU, Uracil, and Tegafur

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The standards of 5-FU and uracil were purchased from Wako Pure Chemical Ind. Ltd. (Osaka, Japan), and the standard of tegafur was purchased from Tokyo Chemical Industry Co. Ltd. (Tokyo, Japan). The stable isotope-labeled internal standards (IS) for 5-FU and tegafur; 5-FU-13C,15N2 and tegafur-13C,15N2, respectively, were synthesized by Toronto Research Chemicals (Toronto, Canada) and that for uracil; uracil-15N2, was synthesized by Cambridge Isotope Laboratories Inc. (Andover, MA, USA). Ammonium formate used for preparing working solution was purchased from Wako Pure Chemical Ind. Ltd. (Osaka, Japan). All solvents (water, methanol, acetonitrile, ethyl acetate, and isopropyl alcohol) used in chromatography, mass spectrometry, liquid extraction, and sample preparation were of the highest analytical quality (HPLC or LC/MS grade).
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3

Synthesis and Characterization of Novel Monomers

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Tegafur was purchased from Tokyo Chemical Industry UK Ltd. (Oxford, UK). 2,6bis(acrylamido)pyridine (BAAPy) [21] and 9-isobutyladenine [22] were synthesised as described previously. All other tested analytes, shown in Figure 1, ethyleneglycol dimethacrylate (EDMA), HPLC grade solvents and deuterated solvents were purchased from Sigma Aldrich (Gillingham, UK). 2,2'-Azobis(2,4-dimethylvaleronitrile) (ABDV) was purchased from Wako Chemicals GmbH and was used as received. Polymerisation inhibitors were removed from EDMA by filtration through a basic alumina column. 1 H NMR spectra were collected on a Bruker ECX 400 MHz NMR spectrometer. An Agilent 1100 HPLC instrument equipped with photodiode array detector and a Phenomenex Kinetex TM C18 column (5μm, 150 mm × 4.6 mm i.d.) was used for all chromatographic separations.
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