反応式
[NH:1]1[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[C:3]([CH2:10][C:11](=O)[C:12]([OH:14])=[O:13])=[CH:2]1.CC1C(O)=C(CN)C(COP(O)(O)=O)=C[N:18]=1.P([O-])([O-])([O-])=O>O>[NH2:18][C@H:11]([C:12]([OH:14])=[O:13])[CH2:10][C:3]1[C:4]2[C:9](=[CH:8][CH:7]=[CH:6][CH:5]=2)[NH:1][CH:2]=1参加物
5
反応条件
- 温度
- 37 °C
実験手順
To a solution containing 20.3 g (100mmol) of indole-3-pyruvic acid and 26.5 g (100 mmol) of pyridoxamine-5-phosphate in 1000 ml of distilled water buffered at pH 6.5 with 0.5M phosphate buffer and maintained at 37° C. is added 50 mg of the monoclonal antibodies prepared according to Example 15. The reaction mixture is gently agitated for 2 hours. The monoclonal antibodies are then recovered by ultrafiltration. Dialysis of the reaction mixture followed by lyophilization yields the product L-tryptophan.
後処理
- additionis added 50 mg of the monoclonal antibodies
- customprepared
- filtrationThe monoclonal antibodies are then recovered by ultrafiltration
- customDialysis of the reaction mixture
出典と根拠
- ORDレコード
- ord-56cee0b26948462bbbd089f8b109a103
- 出典データセット
- uspto-grants-1997_08
- 特許番号
- US05658752
関連ノート
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