Busqueda de Subestructura

368976

COc1ccc(NC(O)=[SH]CCCN2CCN(CCCc3ccc(Cl)cc3)CC2)cc1.COc1ccc(NC(O)=[SH]CCCN2CCN(CCCc3ccc(Cl)cc3)CC2)cc1.Cl.Cl.Cl.Cl.O
Reaction #3932
N-(4-methoxyphenyl)-S-{3-[4-[3-(4-chlorophenyl)propyl]piperazin-1-yl]propyl}thiocarbamate dihydrochloride hemihydrate
Rendimiento 146.1%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C(=O)N[C@H]1CC[C@H](CCN2CCN(c3cccc(Cl)c3Cl)CC2)CC1
Reaction #44398
title compound
Rendimiento 65.0%DOI: 10.6084/m9.figshare.5104873.v1
CCNC(=O)N[C@H]1CC[C@H](CCN2CCN(c3cccc(Cl)c3Cl)CC2)CC1
Reaction #44399
title compound
Rendimiento 65.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C(=O)N[C@H]1CC[C@H](CCN2CCN(c3cccc(Cl)c3Cl)CC2)CC1
Reaction #44400
title compound
Rendimiento 143.6%DOI: 10.6084/m9.figshare.5104873.v1
CCCCN1CCNCC1.Cl.Cl
Reaction #51230
N-butylpiperazine.dihydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(CC(c2cccc3ccccc23)C2CCCCCCC2O)CC1.Cl.Cl
Reaction #57113
2-(4-methylpiperazin-1-yl-1-(1-naphthyl)ethyl]cyclooctanol Dihydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(CC(c2ccc(Oc3ccccc3)cc2)C2(O)CCCCC2)CC1.Cl.Cl
Reaction #57116
1-[2-(4-methylpiperazin-1-yl)-1-(4-phenoxyphenyl)ethyl]cyclohexanol Dihydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(CC(c2ccc(OCc3ccc(C(F)(F)F)cc3)c(F)c2)C2(O)CCCCC2)CC1.Cl.Cl
Reaction #57124
1-[1-(3-fluoro-4-{[4-(trifluoromethyl)benzyl]oxy}phenyl)-2-(4-methylpiperazin-1-yl)ethyl]cyclohexanol Dihydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(COc2ccc(C(CN3CCNCC3)C3(O)CCCCC3)cc2F)cc1.Cl.Cl
Reaction #57125
1-(1-{3-fluoro-4-[(4-methylbenzyl)oxy}phenyl]-2-piperazin-1-ylethyl)cyclohexanol Dihydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)C1CN(CC(=O)Nc2c(Cl)cccc2Cl)CCN1CCCC(=O)C(c1ccccc1)c1ccccc1.O
Reaction #63624
3-(aminocarbonyl)-N-(2,6-dichlorophenyl)-4-(4-oxo-5,5-diphenylpentyl)-1-piperazineacetamide monohydrate
Rendimiento 3.7%DOI: 10.6084/m9.figshare.5104873.v1
O=C(CN1CCN(CCCC(c2ccc(F)cc2)c2ccc(F)cc2)C(C(=O)O)C1)Nc1c(Cl)cccc1Cl
Reaction #63625
1-[4,4-bis(4-fluorophenyl)butyl]-4-[2-[(2,6-dichlorophenyl)amino]-2-oxoethyl]-2-piperazinecarboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
O=c1ccc2ccc(OCCCCN3CCN(c4cccc(Cl)c4Cl)CC3)cc2[nH]1
Reaction #71515
desired product
Rendimiento 102.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C(N1CCCC(CN2CCN(c3ccccc3Cl)CC2)C1)C1(c2ccc(Cl)cc2)CCC1
Reaction #78927
7
Rendimiento 42.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCN1CCN(CCCc2noc3cc(F)ccc23)CC1.Cl.Cl
Reaction #92898
product
Rendimiento 18.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCN1CCN(CCCc2noc3cc(F)ccc23)CC1.Cl.Cl
Reaction #93159
product
Rendimiento 18.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](Nc1cc(N2CCN(C(=O)[C@H]3CCCCN3)CC2)ccc1F)c1ccc(Cl)cc1Cl
Reaction #162316
desired product
Rendimiento 65.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](Nc1cc(N2CCN(C(=O)[C@H]3CCCCN3)CC2)ccc1F)c1ccc(Cl)cc1Cl
Reaction #162317
title compound
Rendimiento 64.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](Nc1cc(N2CCN(C3CCCC(CO)C3)CC2)ccc1Cl)c1ccc(Cl)cc1Cl
Reaction #162318
desired product
Rendimiento 10.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NCCCCC(NC(=O)C(N)Cc1cc(Cl)c(O)c(Cl)c1)C(=O)N1CCN(c2ccncc2)CC1
Reaction #177823
DOI: 10.1039/C8SC04228D
O=C(N1CCCC(CN2CCN(c3ccccc3Cl)CC2)C1)C1(c2ccc(Cl)cc2)CCC1
Reaction #179112
DOI: 10.1039/C8SC04228D
Página 1Siguiente