반응식
[CH3:1]C1N(CCO)C([N+]([O-])=O)=CN=1.CCC(N1N=CN(C2C=CC(N3CCN(C4C=CC(OC[C@@H]5[O:47][C@:46]([C:54]6[CH:55]=[CH:56][C:57](Cl)=C[C:59]=6Cl)(CN6N=CN=C6)[O:45]C5)=CC=4)CC3)=CC=2)C1=O)C.CC[C@@H]1NC(=O)[C@H:104]([C@H:108]([OH:115])[C@@H:109]([CH2:111]/[CH:112]=[CH:113]/[CH3:114])[CH3:110])N(C)C(=O)[C@H](C(C)C)N(C)C(=O)[C@H](CC(C)C)N(C)C(=O)[C@H](CC(C)C)N(C)C(=O)[C@@H](C)NC(=O)[C@H](C)NC(=O)[C@H](CC(C)C)N(C)C(=O)[C@H](C(C)C)NC(=O)[C@H](CC(C)C)N(C)C(=O)CN(C)C1=O.CCN1C(=O)C(=O)N(C(N[C@@H](C(N[C@@H]2C(=O)N3[C@@H](C(O)=O)C(C)(C)S[C@H]23)=O)C2C=CC=CC=2)=O)CC1.CO/N=C(\C(N[C@@H]1C(=O)N2C(C(O)=O)=C(COC(N)=O)CS[C@H]12)=O)/C1OC=CC=1>>[CH3:114][C:113]1[CH:112]=[CH:111][C:109]([CH3:110])=[C:108]([O:115][CH2:57][CH2:56][CH2:55][C:54]([C:46]([OH:45])=[O:47])([CH3:59])[CH3:1])[CH:104]=1참가 물질
6
실험 절차
and finally mainly metronidazole, itraconazole, cyclosporine, piperacilline and cefuroxime.
출처 및 근거
- ORD 기록
- ord-6d75c7bf579040278ede196cfed4d54e
- 출처 데이터셋
- uspto-grants-1998_07
- 특허 번호
- US05776495
연결된 노트
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