Busqueda de Subestructura

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CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cn1
Reaction #10855
8-[3-[N-[(E)-3-(6-acetamidopyridin-3-yl)acryloylglycyl]-N-methylamino]-2,6-dichlorobenzyloxy]-2methylquinoline
Rendimiento 53.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1cc(NC(=O)Nc2ccc(Cl)cc2)n(-c2cccc(C(C)(C)O)c2)n1
Reaction #45257
1-{5-t-butyl-2-[3-(1-hydroxy-1-methyl-ethyl)-phenyl]-2H-pyrazol-3-yl}-3-(4-chloro-phenyl)-urea
Rendimiento 81.5%DOI: 10.6084/m9.figshare.5104873.v1
CCCCc1nn(-c2cc(C(=O)O)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1
Reaction #64548
title compound
Rendimiento 84.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCc1nn(-c2cc(C(=O)N(C)CCCC)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1
Reaction #64549
title compound
Rendimiento 36.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C([O-])c1cc(NS(=O)(=O)c2ccc3c(S(=O)(=O)Nc4cc(C(=O)[O-])cc(C(=O)[O-])c4)cc(S(=O)(=O)Nc4cc(C(=O)[O-])cc(C(=O)[O-])c4)cc3c2)cc(C(=O)[O-])c1.[Na+].[Na+].[Na+].[Na+].[Na+].[Na+]
Reaction #94500
product
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1cc(NS(=O)(=O)c2ccc3c(S(=O)(=O)Nc4cc(C(=O)O)cc(C(=O)O)c4)cc(S(=O)(=O)Nc4cc(C(=O)O)cc(C(=O)O)c4)cc3c2)cc(C(=O)O)c1
Reaction #94505
5,5',5"-[1,3,6-Naphthalenetriyltris(sulfonylimino)]-triisophthalic acid
Rendimiento 97.5%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(S(=O)(=O)Nc2cc(C(=O)Nc3ccccc3)cc(OCC(O)CO)c2Oc2cccc(OC)c2)cc1
Reaction #173757
DOI: 10.1039/C8SC04228D
COCCCN1CCOc2ccc(COC3CN(S(=O)(=O)c4ccc(C)cc4)C(CC(C)(C)C#N)CC3c3ccc(OC)cc3)cc21
Reaction #175468
DOI: 10.1039/C8SC04228D
COC(=N)c1cccc(NC(=O)Nc2ccc(S(=O)(=O)NCc3c(F)ccc(F)c3F)cc2)c1
Reaction #176381
DOI: 10.1039/C8SC04228D
CCOC(=O)c1ccc(NC(=O)c2ccc3c(c2)N(S(=O)(=O)c2cc(C)ccc2OC)CCO3)cc1F
Reaction #177325
DOI: 10.1039/C8SC04228D
COC(=O)c1cc(N)cc(S(C)(=O)=O)c1
Reaction #177714
DOI: 10.1039/C8SC04228D
COC(=O)c1ccc2c(c1)N(S(=O)(=O)c1cc(Cl)ccc1OC)CC2C
Reaction #179108
DOI: 10.1039/C8SC04228D
COCCCN1CCOc2ccc(C(OC3CNC(CO[Si](C(C)C)(C(C)C)C(C)C)CC3c3ccc(COCC(C)COC)cc3)S(=O)(=O)c3ccc(C)cc3)cc21
Reaction #189550
DOI: 10.1039/C8SC04228D
CCOC(=O)c1ccc(NC(=O)c2ccc3c(c2)N(S(=O)(=O)c2cc(Cl)ccc2OC)CC3C)cc1
Reaction #196395
DOI: 10.1039/C8SC04228D
CC1(C)CCN(S(=O)(=O)c2ccccc2)c2cc(C(=O)Cl)ccc2S1
Reaction #198311
DOI: 10.1039/C8SC04228D
COCCCN1CCOc2ccc(COC3CN(S(=O)(=O)c4ccc(C)cc4)C(CC(C)NC(C)=O)CC3c3ccc(OC)cc3)cc21
Reaction #199561
DOI: 10.1039/C8SC04228D
COCCCN1CCOc2ccc(COC3CN(S(=O)(=O)c4ccc(C)cc4)C(CC(C)(C)C(=O)NC4CCN(C)CC4)CC3c3ccc(OC)cc3)cc21
Reaction #201629
DOI: 10.1039/C8SC04228D
CCCCc1nn(-c2cc(C(=O)N(C)CCCC)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1
Reaction #202929
DOI: 10.1039/C8SC04228D
COc1ccc(Cl)cc1S(=O)(=O)N1CCOc2ccc(C(=O)O)cc21
Reaction #204846
DOI: 10.1039/C8SC04228D
CC1(C)CCN(S(=O)(=O)c2ccccc2)c2cc(C(=O)O)ccc2S1
Reaction #206146
DOI: 10.1039/C8SC04228D
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