반응식
[P:1]([O:13][CH2:14][C@H:15]1[O:19][C@@H:18]([N:20]2[C:30]3[N:29]=[C:27]([NH2:28])[NH:26][C:24](=[O:25])[C:23]=3[N:22]=[CH:21]2)[C@H:17]([OH:31])[C@@H:16]1[OH:32])([O:4][P:5]([O:8][P:9]([OH:12])([OH:11])=[O:10])([OH:7])=[O:6])(=[O:3])[OH:2].S(OC)(O[CH3:37])(=O)=O>>[CH3:37][N:22]1[C:23]2[C:24]([N:26]=[C:27]([NH2:28])[NH:29][C:30]=2[N+:20]([C@@H:18]2[O:19][C@H:15]([CH2:14][O:13][P:1]([O:4][P:5]([O:8][P:9]([OH:11])([OH:12])=[O:10])([OH:7])=[O:6])([OH:2])=[O:3])[C@@H:16]([OH:32])[C@H:17]2[OH:31])=[CH:21]1)=[O:25].[CH2:30]([NH+:20]([CH2:18][CH3:17])[CH2:21][CH3:37])[CH3:23]참가 물질
실험 절차
Guanosine triphosphate (GTP) (300 mg, 0.5 mmol) was methylated using dimethyl sulfate according to the procedure of Hendler et al. ((1970) Biochemistry 9, 414) with modification. The reaction mixture was neutralized and the product purified on a DEAE Sephadex A-25 (Sephadex is a registered trademark of Pharmacia Fine Chemicals, Inc.) column (3×50 cm). The column was washed with water and then eluted with a linear gradient of 0 to 0.8M triethylammonium bicarbonate (TEAB), pH 7.8 (2 l total volume). Twenty-milliliter fractions were collected and assayed spectrophometrically at 260 nm. m7GTP eluted at approximately 0.4M, and the peak was pooled and repeatedly evaporated to dryness from water vacuo. m7GTP-triethylammonium salt was obtained as a white solid (0.25 mmol, 50% yield).
후처리
- customthe product purified on a DEAE Sephadex A-25 (Sephadex
- washThe column was washed with water
- washeluted with a linear gradient of 0 to 0.8M triethylammonium bicarbonate (TEAB), pH 7.8 (2 l total volume)
- customTwenty-milliliter fractions were collected
- washm7GTP eluted at approximately 0.4M
- customrepeatedly evaporated to dryness from water vacuo
출처 및 근거
- ORD 기록
- ord-0bbd8c4c618047118d9ee8b27e01bd24
- 출처 데이터셋
- uspto-grants-1987_12
- 특허 번호
- US04710566
연결된 노트
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