子结构搜索

4023

C[N+](C)(CC1=C(C(=O)[O-])N2C(=O)[C@@H](N)[C@H]2SC1)Cc1cc(=O)c(O)c[nH]1.Cl.Cl
Reaction #5615
7β-amino-3-[N,N-dimethyl-N-{(5-hydroxy-4-oxo-1,4-dihydropyridin-2-yl)methyl}ammonio]methyl-3-cephem-4carboxylate dihydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
C[N+]1(CC2=C(C(=O)[O-])N3C(=O)[C@@H](NC(=O)C(=NOCC(=O)O)c4csc(N)n4)[C@H]3SC2)CCNCC1
Reaction #5622
7β-[2-(2-aminothiazol- 4-yl)-2-carboxymethoxyiminoacetamido]-3-(1-methyl-1-piperazinio)methyl-3-cephem-4-carboxylate
收率 26.7%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc[n+](CC2=C(C(=O)[O-])N3C(=O)C(NC(=O)C(=NOC(F)F)c4csc(N)n4)[C@H]3SC2)cc1
Reaction #62779
7-[2-(2-aminothiazol-4-yl)-2-difluoromethoxyiminoacetamido]-3-(4-methoxy-1-pyridiniomethyl)-3-cephem-4-carboxylate
收率 13.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CC1(c2ccc(Br)cc2)c2ccccc2-c2[nH+]ccn21.O=C([O-])C(F)(F)F
Reaction #74445
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(CC1(c2ccc(Br)cc2)c2ccccc2-c2nccn21)N1CCCC1
Reaction #74446
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NCC1(c2ccc(Br)cc2)c2ccccc2-c2nccn21
Reaction #74447
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC[NH+](CC)CC.COc1ccc(-c2ccccc2N(CCCOC(=O)COCC(=O)[O-])c2ccccc2)cc1
Reaction #76244
solution
DOI: 10.6084/m9.figshare.5104873.v1
O=C([O-])c1cccnc1NCC1CCN(c2ccncc2)CC1.[NH4+]
Reaction #78128
title compound
收率 96.7%DOI: 10.6084/m9.figshare.5104873.v1
Nc1cc2nc(NCc3ccccc3)ncc2cn1
Reaction #79083
7-amino-2-benzylaminopyrido[4,3-d]pyrimidine
收率 73.3%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)O.Nc1cc2ncnc(NCc3ccc(Cl)cc3)c2cn1
Reaction #79088
7-Amino-4-(4-chlorobenzylamino)pyrido[4,3-d]pyrimidine Mesylate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@@H](CN(c1ccccc1)c1ncccn1)C(=O)O
Reaction #84246
(S)-2-tert-butoxycarbonylamino-3-(phenyl-pyrimidin-2-ylamino)-propanoic acid
收率 95.4%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](OC(C)(C)C)[C@@H](CO)NC(=O)OCc1ccccc1
Reaction #85781
benzyl((2R)-(3R)-3-(tert-butoxy)-1-hydroxybutan-2-yl)carbamate
DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C(=O)CC1(O)C(=O)Nc2ccc(I)cc21
Reaction #158214
2-(3-Hydroxy-5-iodo-2-oxo-2,3-dihydro-1H-indol-3-yl)-N,N-dimethyl-acetamide
DOI: 10.6084/m9.figshare.5104873.v1
N[C@@H](Cc1ccccc1)C(=O)O[C@H]1C[N+]2(CCOc3ccccc3)CCC1CC2.N[C@@H](Cc1ccccc1)C(=O)O[C@H]1C[N+]2(CCOc3ccccc3)CCC1CC2.O=C([O-])C(F)(F)F.O=C([O-])C(F)(F)F
Reaction #164213
title compound
收率 43.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(C)c1cccc([N+](=O)[O-])c1
Reaction #175337
DOI: 10.1039/C8SC04228D
O=C(C[n+]1ccc(CN2CCC(=CC3=C(C(=O)[O-])N4C(=O)C(NC(=O)CBr)C4SC3)C2=O)cc1)Nc1ccc(O)c(F)c1
Reaction #243591
DOI: 10.1039/C8SC04228D
O=C(C[n+]1ccc(CN2CCC(=CC3=C(C(=O)[O-])N4C(=O)C(NC(=O)CSc5ccncc5)C4SC3)C2=O)cc1)Nc1ccc(O)cc1
Reaction #258089
DOI: 10.1039/C8SC04228D
O=C(C[n+]1ccc(CN2CCC(=CC3=C(C(=O)[O-])N4C(=O)C(NC(=O)CSc5ccc(O)cc5)C4SC3)C2=O)cc1)Nc1ccc(O)c(F)c1
Reaction #259275
DOI: 10.1039/C8SC04228D
O=C(C[n+]1ccc(CN2CCC(=CC3=C(C(=O)[O-])N4C(=O)C(NC(=O)CSc5ccc(Cl)c(Cl)c5)C4SC3)C2=O)cc1)Nc1ccc(O)c(F)c1
Reaction #300622
DOI: 10.1039/C8SC04228D
NC(=O)c1cc[n+](CC2=C(C(=O)[O-])N3C(=O)[C@@H](NC(=O)C(c4ccccc4)S(=O)(=O)[O-])[C@H]3SC2)cc1.[Na+]
Reaction #305475
cefsulodin sodium
DOI: 10.6084/m9.figshare.5104873.v1
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