化工社化工社 化学情報印刷レポート · 研究参考用
Thymidine → Deoxyguanosine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Thymidine | HCID 5789 | — |
| 反応物 | 5-Methylbarbituric acid | HCID 232791 | — |
| 反応物 | Thymin Uracil | HCID 23504037 | — |
| 反応物 | Guanine | HCID 135398634 | — |
| 生成物 | Deoxyguanosine | HCID 135398592 | 75% |
反応手順
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.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06017736 |
| 出典データセット | uspto-grants-2000_01 |
| ORD ID | ord-6a28f6a7a4b74260806849e9f9de53d4 |
| 出典メモ | uspto-grants-2000_01 |