化工社化工社 化学情報印刷レポート · 研究参考用
Dihydropyrimidine → Tegafur
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Dihydropyrimidine | HCID 1056 | — |
| 反応物 | 5-Fluorouracil | HCID 3385 | — |
| 反応物 | NADPH | HCID 5884 | — |
| 反応物 | alpha-Fluoro-beta-alanine | HCID 13351 | — |
| 反応物 | Doxifluridine | HCID 18343 | — |
| 反応物 | 5,6-Dihydro-5-fluorouracil | HCID 121997 | — |
| 反応物 | Ammonium Acetate | HCID 517165 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | Tegafur | HCID 5386 | — |
| 生成物 | Capecitabine | HCID 60953 | — |
反応手順
100 μM NADPH and 25 μl of cell supernatant (reaction volume; 50 μl) were incubated at 37° C. for 30 min. After the reaction, 5 μl of the reaction solution was subjected to thin layer chromatography (Silica gel 60F254; Merck, Germany) and developed with a mixed solution of ethanol and 1 M ammonium acetate (5:1, v/v). Dihydropyrimidine dehydrogenase activity was determined by measuring the sum of dihydrofluorouracil and 2-fluoro-β-alanine dissociated from [6-14C] 5-FU with a liquid scintillation counter. Drugs used: UFT, TS-1 and capecitabine were synthesized by Taiho Pharmaceutical Co., Ltd. 5′-DFUR was purchased from Roche Japan. [6-14C]-5-FU (1.85 GBq/mmol) was purchased from Moravek Biochemicals, Inc. (Brea, Calif., USA).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08440398B2 |
| 出典データセット | uspto-grants-2013_05 |
| ORD ID | ord-08bf9dab220c4455a76fa5eff9def14f |
| 出典メモ | uspto-grants-2013_05 |