돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2091456생성일: 2026년 10월 27일

Dihydropyrimidine → Tegafur

https://huagongshe.com/reaction/2091456

반응식

참여 물질

역할이름HCID투입량
반응물DihydropyrimidineHCID 1056—
반응물5-FluorouracilHCID 3385—
반응물NADPHHCID 5884—
반응물alpha-Fluoro-beta-alanineHCID 13351—
반응물DoxifluridineHCID 18343—
반응물5,6-Dihydro-5-fluorouracilHCID 121997—
반응물Ammonium AcetateHCID 517165—
용매EthanolHCID 702—
생성물TegafurHCID 5386—
생성물CapecitabineHCID 60953—

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08440398B2
출처 데이터셋uspto-grants-2013_05
ORD IDord-08bf9dab220c4455a76fa5eff9def14f
출처 메모uspto-grants-2013_05