反応式
[S:1]([OH:5])(O)(=[O:3])=[O:2].[NH2:6][CH:7]([CH2:9][C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1)[CH3:8].[NH2:16][C@H:17]([C:23](O)=[O:24])[CH2:18][CH2:19][CH2:20][CH2:21][NH2:22].[CH3:26][C@H](N)CC1C=CC=CC=1.[CH3:36][C@H](N)CC1C=CC=CC=1>O>[CH3:8][C@H:7]([NH:6][C:23]([C@@H:17]([NH2:16])[CH2:18][CH2:19][CH2:20][CH2:21][NH2:22])=[O:24])[CH2:9][C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1.[CH3:26][S:1]([OH:5])(=[O:3])=[O:2].[CH3:36][S:1]([OH:5])(=[O:3])=[O:2]参加物
5
実験手順
Male Sprague-Dawley rats were provided water ad libitum, fasted overnight, and dosed by oral gavage with 1.5, 3, 6, 12, and 60 mg/kg of amphetamine sulfate or L-lysine-d-amphetamine containing the equivalent amounts of d-amphetamine. Concentrations of d-amphetamine were measured by ELISA.
出典と根拠
- ORDレコード
- ord-6924bb117ee8494c94c27f4be6a83ed0
- 出典データセット
- uspto-grants-2010_02
- 特許番号
- US07655630B2
関連ノート
読み込み中…