Busqueda de Subestructura

794416

CC(C)(O)Cn1ccc(NC(=O)C(CC2CCOCC2)N2CC(Oc3ccccc3Br)=CC2=O)n1
Reaction #47699
2-[4-(2-bromo-phenoxy)-2-oxo-2,5-dihydro-pyrrol-1-yl]-N-[1-(2-hydroxy-2-methyl-propyl)-1H-pyrazol-3-yl]-3-(tetrahydro-pyran-4-yl)-propionamide
Rendimiento 35.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(Oc2cc(O[C@@H](C)CO)cc(C(=O)Nc3ccn(C)n3)c2)cc1F
Reaction #48807
desired compound
Rendimiento 30.9%DOI: 10.6084/m9.figshare.5104873.v1
COC[C@H](C)Oc1cc(Oc2ccc(S(=O)(=O)N(C)C)cc2)cc(C(=O)Nc2ccn(C)n2)c1
Reaction #48821
title compound
Rendimiento 32.3%DOI: 10.6084/m9.figshare.5104873.v1
COC[C@H](C)Oc1cc(Oc2ccc(S(=O)(=O)N(C)C)cc2Cl)cc(C(=O)Nc2ccn(C)n2)c1
Reaction #48822
title compound
Rendimiento 688.3%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](CO)Oc1cc(Oc2ccc(C(=O)N3CCCCC3)cc2)cc(C(=O)Nc2ccn(C)n2)c1
Reaction #48844
desired compound
Rendimiento 71.2%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](CO)Oc1cc(Oc2ccc(C(=O)O)cc2)cc(C(=O)Nc2ccn(C)n2)c1
Reaction #48845
desired compound
Rendimiento 108.7%DOI: 10.6084/m9.figshare.5104873.v1
COC[C@H](C)Oc1cc(Oc2ccc(C(=O)/C=C/N(C)C)cc2)cc(C(=O)Nc2ccn(C)n2)c1
Reaction #48873
desired product
Rendimiento 83.3%DOI: 10.6084/m9.figshare.5104873.v1
COC[C@H](C)Oc1cc(Oc2ccc(C(C)=O)cc2)cc(C(=O)Nc2ccn(C)n2)c1
Reaction #48874
desired product
Rendimiento 49.8%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(N(C)c2ccn(-c3ccccc3)n2)cc(C)c1O
Reaction #50553
title product
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)C(=O)Oc1c(C)cc(Nc2ccn(-c3ccccc3)n2)cc1C
Reaction #50556
2,6-Dimethyl-4-(1-phenyl-1H-pyrazol-3-yl)aminophenyl 2-oxopropanoate
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(Nc2ccn(-c3ccccc3)n2)cc(C)c1OC(=O)CC#N
Reaction #50557
2,6-Dimethyl-4-(1-phenyl-1H-pyrazol-3-yl)aminophenyl cyanoacetate
DOI: 10.6084/m9.figshare.5104873.v1
O=CNc1cc(-c2ccc(Cl)cc2)n(-c2ccc(Cl)cc2Cl)n1
Reaction #83638
formamide
DOI: 10.6084/m9.figshare.5104873.v1
CCCc1cccc(-c2cc(N)nn2-c2ccccc2)c1
Reaction #170697
titled compound
Rendimiento 47.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCc1cccc(-c2cc(NC(=O)C3CCC(=O)NC3)nn2-c2ccccc2)c1
Reaction #170698
titled compound
Rendimiento 61.5%DOI: 10.6084/m9.figshare.5104873.v1
CCCc1cccc(-c2cc(NC(=O)[C@H]3CNC(=O)N3C)nn2-c2ccccc2)c1
Reaction #170702
titled compound
Rendimiento 49.1%DOI: 10.6084/m9.figshare.5104873.v1
CCCc1cccc(-c2cc(NC(=O)C3COC(=O)C3)nn2-c2ccccc2)c1
Reaction #170705
titled compound
Rendimiento 62.7%DOI: 10.6084/m9.figshare.5104873.v1
CCCc1cccc(-c2cc(NC(=O)[C@@H](CNC(=O)OC(C)(C)C)NC(=O)OC(C)(C)C)nn2-c2ccccc2)c1
Reaction #170706
titled compound
Rendimiento 91.5%DOI: 10.6084/m9.figshare.5104873.v1
CCCc1cccc(-c2cc(NC(=O)[C@H](N)CN)nn2-c2ccccc2)c1.Cl.Cl
Reaction #170707
titled compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCc1cccc(-c2cc(NC(=O)[C@H]3CNC(=O)N3)nn2-c2ccccc2)c1
Reaction #170708
titled compound
Rendimiento 47.2%DOI: 10.6084/m9.figshare.5104873.v1
CCCCc1cccc(-c2cc(N)nn2-c2ccccc2)c1
Reaction #170746
titled compound
Rendimiento 86.1%DOI: 10.6084/m9.figshare.5104873.v1
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