反応式
[CH:1]1[C:6]([CH:7]2[O:16][C:15]3[CH:14]=[C:13]([OH:17])[CH:12]=[C:11]([OH:18])[C:10]=3[CH2:9][CH:8]2[OH:19])=[CH:5][C:4]([OH:20])=[C:3]([OH:21])[CH:2]=1.OO>CC(C)=O>[CH2:9]1[C:10]2[C:15](=[CH:14][C:13]([OH:17])=[CH:12][C:11]=2[OH:18])[O:16][C@H:7]([C:6]2[CH:1]=[C:1]3[C:6]([C@H:7]4[O:16][C:15]5[C:10](=[C:11]([OH:18])[CH:12]=[C:13]([OH:17])[CH:14]=5)[CH2:9][C@@H:8]4[OH:19])=[CH:5][C:4]([OH:20])=[C:3]([OH:21])[C:2]3=[C:3]([OH:21])[C:4](=[O:20])[CH:5]=2)[C@@H:8]1[OH:19]参加物
4
実験手順
C (catechin) (0.8 g) and EGC (0.8 g) were dissolved in a mixture of acetone-pH 5.0 phosphate citrate buffer (1:10, v/v, 50 mL), which contained 4 mg horseradish peroxidase. While being stirred, 2.0 mL of 3.13% H2O2 was added four times during 45 minutes. The reaction mixture was extracted by ethyl acetate (50 mL×3). After concentration, the residue was subjected to Sephadex LH 20 column eluted with acetone-water solvent system (45%). 120 mg neotheaflavin was obtained.
後処理
- extractionThe reaction mixture was extracted by ethyl acetate (50 mL×3)
- concentrationAfter concentration
- washeluted with acetone-water solvent system (45%)
出典と根拠
- ORDレコード
- ord-84eb41263ae14b84ab4221d7a1a26762
- 出典データセット
- uspto-grants-2007_10
- 特許番号
- US07288680B2
関連ノート
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