반응식
[CH3:1][C:2]1([CH3:25])[S:6][C@@H:5]2[C@H:7]([NH:10][C:11]([C@H:13]([NH2:21])[C:14]3[CH:15]=[CH:16][C:17]([OH:20])=[CH:18][CH:19]=3)=[O:12])[C:8](=[O:9])[N:4]2[C@H:3]1[C:22]([OH:24])=[O:23].O.C(N=C=NCCCN(C)C)C.[CH:38]1[C:43]([NH2:44])=[CH:42][C:41]2[C:45]([O:47][C:48]3([C:58]4[CH:59]=[CH:60][C:61]([OH:63])=[CH:62][C:57]=4[O:56][C:50]4[CH:51]=[C:52]([OH:55])[CH:53]=[CH:54][C:49]3=4)[C:40]=2[CH:39]=1)=[O:46]>C(#N)C>[CH:38]1[C:43]([NH2:44])=[CH:42][C:41]2[C:45]([O:47][C:48]3([C:58]4[CH:59]=[CH:60][C:61]([OH:63])=[CH:62][C:57]=4[O:56][C:50]4[CH:51]=[C:52]([OH:55])[CH:53]=[CH:54][C:49]3=4)[C:40]=2[CH:39]=1)=[O:46].[CH3:1][C:2]1([CH3:25])[S:6][C@@H:5]2[C@H:7]([NH:10][C:11]([C@H:13]([NH2:21])[C:14]3[CH:19]=[CH:18][C:17]([OH:20])=[CH:16][CH:15]=3)=[O:12])[C:8](=[O:9])[N:4]2[C@H:3]1[C:22]([OH:24])=[O:23]참가 물질
6
실험 절차
Fluoresceinamine (FA; 0.0583 g) was dissolved in 1.0 ml acetonitrile to from a FA solution. Amoxicillin (0.1 g) was dissolved in 30 ml deionized water, and mixed with the aforesaid FA solution. 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide (0.0408 g) was added thereto and magnetically stirred at room temperature in the dark for 12 hours to make FA to graft to the carboxyl group of amoxicillin to form a fluorescent-labeled FA-amoxicillin. And, finally, the sample was freeze-dried to collect the fluorescent-labeled FA-amoxicillin.
출처 및 근거
- ORD 기록
- ord-adb1b15315a040e0ac32635795454c18
- 출처 데이터셋
- uspto-grants-2014_07
- 특허 번호
- US08790695B2
연결된 노트
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