Busqueda de Subestructura

Cc1cccc(C)c1

CCN1CCC(N(CC)Cc2cccc(-c3ccnc(NCCc4ccc(O)c(Cl)c4)n3)c2)CC1
Reaction #43141
2-Chloro-4-{2-[4-(3-{[ethyl-(-ethyl-piperidin-4-yl)-amino]-methyl}-phenyl)-pyrimidin-2-ylamino]-ethyl}-phenol
DOI: 10.6084/m9.figshare.5104873.v1
CCCN1CCC(N(CC)Cc2cccc(-c3ccnc(NCCc4ccc(O)c(Cl)c4)n3)c2)CC1
Reaction #43142
2-Chloro-4-{2-[4-(3-{[ethyl-(1-propyl-piperidin-4-yl)-amino]-methyl}-phenyl)-pyrimidin-2-ylamino]-ethyl}-phenol
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCOc1nc(OCCCCCCCCCCCC)nc(Oc2cc(-c3ccccc3)c(O)c(-c3ccccc3)c2)n1
Reaction #54159
6-(4-hydroxy-3,5-diphenylphenoxy)-2,4-dilauroxys-triazine
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCCCCOc1nc(OCCCCCCCCCCCCCCCCCC)nc(Oc2cc(-c3ccccc3)c(O)c(-c3ccccc3)c2)n1
Reaction #54160
6-(4-hydroxy-3,5-diphenyphenoxy)-2,4-distearoxy-s-triazine
DOI: 10.6084/m9.figshare.5104873.v1
c1ccc(-c2c(-c3cccc4ccccc34)cc(-c3ccc(-c4cc(-c5cccc6ccccc56)cc(-c5cccc6ccccc56)c4)cc3)cc2-c2cccc3ccccc23)cc1
Reaction #75456
solid
Rendimiento 81.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)OC(=O)Nc2c(F)cc(-c3ccc(F)c(Cl)c3)cc21
Reaction #78996
6-(3-chloro-4-fluoro-phenyl)-8-fluoro-4,4-dimethyl-1,4-dihydrobenzo[d][1,3]oxazin-2-one
Rendimiento 66.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)OC(=O)Nc2ccc(-c3ccc(C#N)c(F)c3)cc21
Reaction #79006
title compound
Rendimiento 6.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)OC(=O)Nc2ccc(-c3ccc(CC#N)c(F)c3)cc21
Reaction #79024
4-(4,4-Dimethyl-2-oxo-1,4-dihydro-2H-benzo[d][1,3]oxazin-6-yl)-2-fluorophenylacetonitrile
DOI: 10.6084/m9.figshare.5104873.v1
CC(NCc1ccc2ccccc2c1)C(Cc1ccc(-c2ccccc2)cc1)c1ccc(Cl)cc1
Reaction #81144
N-{(1RS, 2RS)-3-(4-biphenylyl)-2-(4- chlorophenyl)-1-methylpropyl}-2-naphthylmethylamine
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cccc(C2C=C(C(F)(F)F)NC3=C2C(=O)CCC3)c1
Reaction #82736
title compound
Rendimiento 55.2%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cccc(C2C=C(C(F)(F)F)NC3=C2C(=O)CCC3)c1
Reaction #82739
title compound
Rendimiento 99.0%DOI: 10.6084/m9.figshare.5104873.v1
NCc1cc(-c2nn(-c3ccc(F)c(Cl)c3)c(=O)[nH]2)c(Cl)cc1F
Reaction #87662
desired product
Rendimiento 42.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)C(=O)NCc1cc(-c2nn(-c3ccc(F)c(Cl)c3)c(=O)[nH]2)c(Cl)cc1F
Reaction #87814
desired product
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-n2nc(-c3cc(CNC(=O)C(C)(C)C)c(F)cc3Cl)[nH]c2=O)cc1Cl
Reaction #87818
desired product
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(-n2nc(-c3cc(CNC(=O)C(C)(C)C)ccc3Cl)[nH]c2=O)ccc1Cl
Reaction #87837
desired product
Rendimiento 37.6%DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)c1cc(-c2ccc(F)cc2)cc2c(C3CCN(S(=O)(=O)CCCCl)CC3)c[nH]c12
Reaction #175702
DOI: 10.1039/C8SC04228D
CCCN1CCC(N(CC)Cc2cccc(-c3ccnc(NCCc4ccc(O)c(Cl)c4)n3)c2)CC1
Reaction #179195
DOI: 10.1039/C8SC04228D
CC(=O)c1ccc(OCc2ccc(Cc3cccc(-c4nn[nH]n4)c3)cc2)c(C(C)C)c1O
Reaction #189991
DOI: 10.1039/C8SC04228D
COC(=O)CNC(=O)c1cccc(C=CC(=O)c2c(OC)cc(C)n(C)c2=O)c1
Reaction #190305
DOI: 10.1039/C8SC04228D
CCOC(=O)c1cnc2c(CNCc3ccccc3)cc(CN3CCOCC3)cc2c1O
Reaction #192605
DOI: 10.1039/C8SC04228D
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