Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Thymidine → Deoxyguanosine
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Thymidine | HCID 5789 | — |
| 반응물 | 5-Methylbarbituric acid | HCID 232791 | — |
| 반응물 | Thymin Uracil | HCID 23504037 | — |
| 반응물 | Guanine | HCID 135398634 | — |
| 생성물 | Deoxyguanosine | HCID 135398592 | 75% |
반응 단계
FIG. 1 shows formation of 5-methyl barbituric acid. Since the acid is decomposed so as to disappear, it has been clarified that uracil thymine dehydrogenase and barbiturase are present in the uracil·thymine decomposing enzyme. In the case of FIG. 1, thymidine disappeared substantially completely, though the starting material guanine was found to remain only slightly. Deoxyguanosine was formed in an amount of 14.9 mM (yield of 75%). Compared with FIG. 2 covering the case where uracil·thymine decomposing enzyme solution was not present, FIG. 1 supports that the desired product of deoxyguanosine was formed in a very large amount.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US06017736 |
| 출처 데이터셋 | uspto-grants-2000_01 |
| ORD ID | ord-6a28f6a7a4b74260806849e9f9de53d4 |
| 출처 메모 | uspto-grants-2000_01 |