Recherche de Sous-structure

804218

CN1C(C(=O)Nc2ccccn2)=C([O-])c2ccccc2S1(=O)=O.[K+]
Reaction #65342
piroxicam potassium
Rendement 84.3%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCC(=O)OC(C)OC1=C(C(=O)Nc2ccccn2)N(C)S(=O)(=O)c2ccccc21
Reaction #185606
DOI: 10.1039/C8SC04228D
CN1C(C(=O)Nc2ncccc2O)=C(O)c2ccc3ccccc3c2S1(=O)=O
Reaction #275468
DOI: 10.1039/C8SC04228D
CN1C(C(=O)Nc2ccccn2)=C(O)c2ccc3ccccc3c2S1(=O)=O
Reaction #276251
DOI: 10.1039/C8SC04228D
COC(=O)C(C)(C)C(=O)OCOC1=C(C(=O)Nc2ccccn2)N(C)S(=O)(=O)c2ccccc21
Reaction #380196
DOI: 10.1039/C8SC04228D
CN1C(C(=O)Nc2ccccn2)=C(O)c2ccccc2S1(=O)=O
Reaction #385048
DOI: 10.1039/C8SC04228D
CN1C(C(=O)Nc2ccccn2)=C(O)c2ccccc2S1(=O)=O
Reaction #441818
piroxicam
Rendement 96.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1C(C(=O)Nc2ccccn2)=C(O)c2ccccc2S1(=O)=O
Reaction #441823
4-hydroxy-2-methyl-N-2-pyridyl-2H-1,2-benzothiazine-3-carboxamide 1,1-dioxide
DOI: 10.6084/m9.figshare.5104873.v1
CN1C(C(=O)Nc2ccccn2)=C(O)c2ccccc2S1(=O)=O
Reaction #572659
Piroxicam
DOI: 10.6084/m9.figshare.5104873.v1
CN1C(C(=O)Nc2ccccn2)=C(O)c2ccccc2S1(=O)=O.N=C(N)NCCC[C@H](N)C(=O)O.OC[C@H]1O[C@@H]2O[C@H]3[C@H](O)[C@@H](O)[C@@H](O[C@H]4[C@H](O)[C@@H](O)[C@@H](O[C@H]5[C@H](O)[C@@H](O)[C@@H](O[C@H]6[C@H](O)[C@@H](O)[C@@H](O[C@H]7[C@H](O)[C@@H](O)[C@@H](O[C@H]8[C@H](O)[C@@H](O)[C@@H](O[C@H]1[C@H](O)[C@H]2O)O[C@@H]8CO)O[C@@H]7CO)O[C@@H]6CO)O[C@@H]5CO)O[C@@H]4CO)O[C@@H]3CO
Reaction #682789
Piroxicam β-Cyclodextrin Arginine
DOI: 10.6084/m9.figshare.5104873.v1
CN1C(C(=O)Nc2ccccn2)=C(O)c2ccccc2S1(=O)=O.N=C(N)NCCC[C@H](N)C(=O)O.OC[C@H]1O[C@@H]2O[C@H]3[C@H](O)[C@@H](O)[C@@H](O[C@H]4[C@H](O)[C@@H](O)[C@@H](O[C@H]5[C@H](O)[C@@H](O)[C@@H](O[C@H]6[C@H](O)[C@@H](O)[C@@H](O[C@H]7[C@H](O)[C@@H](O)[C@@H](O[C@H]8[C@H](O)[C@@H](O)[C@@H](O[C@H]1[C@H](O)[C@H]2O)O[C@@H]8CO)O[C@@H]7CO)O[C@@H]6CO)O[C@@H]5CO)O[C@@H]4CO)O[C@@H]3CO
Reaction #682790
Piroxicam β-Cyclodextrin Arginine
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)OC(=O)CN1C(=O)c2ccccc2S1(=O)=O
Reaction #761072
DOI: 10.1039/C8SC04228D
CN1C(C(=O)Nc2ccccn2)=C(OC(=O)C=Cc2ccccc2)c2ccccc2S1(=O)=O
Reaction #832840
4-cinnamoyloxy-2-methyl-N-(2-pyridyl)-2H-1,2-benzothiazine-3-carboxamide 1,1-dioxide
DOI: 10.6084/m9.figshare.5104873.v1
CN1C(C(=O)Nc2ccccn2)=C(OC2OC(=O)c3ccccc32)c2ccccc2S1(=O)=O
Reaction #1034991
DOI: 10.1039/C8SC04228D
CCCCCCCC(=O)OCOC1=C(C(=O)Nc2ccccn2)N(C)S(=O)(=O)c2ccccc21
Reaction #1047051
DOI: 10.1039/C8SC04228D
CN1C(C(=O)Nc2ccccn2)=C(O)c2ccccc2S1(=O)=O
Reaction #1301985
DOI: 10.1039/C8SC04228D
CN1C(C(=O)Nc2ccccn2)=C(O)c2ccccc2S1(=O)=O
Reaction #1321077
DOI: 10.1039/C8SC04228D
CN1C(C(=O)Nc2ccccn2)=C(O)c2ccccc2S1(=O)=O.N=C(N)NCCC[C@H](N)C(=O)O.OC[C@H]1O[C@@H]2O[C@H]3[C@H](O)[C@@H](O)[C@@H](O[C@H]4[C@H](O)[C@@H](O)[C@@H](O[C@H]5[C@H](O)[C@@H](O)[C@@H](O[C@H]6[C@H](O)[C@@H](O)[C@@H](O[C@H]7[C@H](O)[C@@H](O)[C@@H](O[C@H]8[C@H](O)[C@@H](O)[C@@H](O[C@H]1[C@H](O)[C@H]2O)O[C@@H]8CO)O[C@@H]7CO)O[C@@H]6CO)O[C@@H]5CO)O[C@@H]4CO)O[C@@H]3CO
Reaction #1342589
Piroxicam β-cyclodextrin arginine
DOI: 10.6084/m9.figshare.5104873.v1
CN1C(C(=O)Nc2ccccn2)=C(O)c2ccccc2S1(=O)=O.N=C(N)NCCC[C@H](N)C(=O)O.OC[C@H]1O[C@@H]2O[C@H]3[C@H](O)[C@@H](O)[C@@H](O[C@H]4[C@H](O)[C@@H](O)[C@@H](O[C@H]5[C@H](O)[C@@H](O)[C@@H](O[C@H]6[C@H](O)[C@@H](O)[C@@H](O[C@H]7[C@H](O)[C@@H](O)[C@@H](O[C@H]8[C@H](O)[C@@H](O)[C@@H](O[C@H]1[C@H](O)[C@H]2O)O[C@@H]8CO)O[C@@H]7CO)O[C@@H]6CO)O[C@@H]5CO)O[C@@H]4CO)O[C@@H]3CO
Reaction #1342590
Piroxicam β-cyclodextrin arginine
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccnc(NC(=O)C2=C(O)c3ccc4ccccc4c3S(=O)(=O)N2C)c1
Reaction #1633143
DOI: 10.1039/C8SC04228D
Page 1Suivant