著者
仲井 由宣 山本 恵司 寺田 勝英 内田 武 清水 昶幸 西垣 貞男
出版者
The Pharmaceutical Society of Japan
雑誌
Chemical and Pharmaceutical Bulletin (ISSN:00092363)
巻号頁・発行日
vol.30, no.7, pp.2629-2632, 1982-07-25 (Released:2008-03-31)
参考文献数
5
被引用文献数
9 14

The crystal structure of ftorafur, C8H9FN2O3, has been determined by single-crystal X-ray diffraction techniques. The crystal is triclinic, space group P1 ; its unit-cell dimensions are a=8.994 (8), b=16.612 (9), c=5.981 (5) Å, α=86.40 (6), β=94.06 (15), γ=80.29 (8)°, Z=4. The structure was solved by the direct method and the final R value was 0.056.
著者
内田 武 米持 悦生 小口 敏夫 寺田 勝英 山本 恵司 仲井 由宣
出版者
The Pharmaceutical Society of Japan
雑誌
Chemical and Pharmaceutical Bulletin (ISSN:00092363)
巻号頁・発行日
vol.41, no.9, pp.1632-1635, 1993-09-15 (Released:2008-03-31)
参考文献数
15
被引用文献数
13 20

Four crystalline forms of tegafur were prepared by recrystallization from different solvents (α-, β-, δ-forms) and by heating (γ-form). They have been characterized using powder X-ray diffraction, thermal analysis, microscopy, density measurements and infrared spectroscopy. From differential scanning calorimetry measurements, it was confirmed that the γ- and δ-forms melted at 175°C and 165°C, whereas the α- and β-forms transformed into the γ-form at about 162°C and 120°C, respectively. The infrared absorption spectral differences observed between the α- and β-forms were discussed in relation to their intermolecular hydrogen bonding systems. It was also found that the difference in crystal forms significantly altered the dissolution rate of tegafur.