Busqueda de Subestructura

1286079

O=C1NCC2CN(C(=O)c3cc4ccccc4n3Cc3ccc(Cl)cc3)CCC12
Reaction #170859
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1cc2ccccc2n1Cc1ccc(Cl)cc1)N1CCC2C(=O)N(Cc3ccccc3)CC2C1
Reaction #170860
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CC2(C(=O)N[C@@H](Cc3ccc(N4C(=O)C5CCNCC5C4=O)cc3)C(=O)O)CCCC2)cc1
Reaction #480620
N-[[1-[(4-methoxyphenyl)methyl]cyclopentyl]carbonyl]-4-[(3aRS, 7aRS)-(octahydro-1,3-dioxo-1H-pyrrolo[3,4-c]pyridin-2-yl)]-L-phenylalanine
Rendimiento 13.8%DOI: 10.6084/m9.figshare.5104873.v1
CN1C(=O)C2C3CCC(C2C1=O)N1COc2ccccc2N=C31
Reaction #548508
title compound
Rendimiento 78.1%DOI: 10.6084/m9.figshare.5104873.v1
CN1C(=O)C2CC3=Nc4cc(Cl)ccc4OCN3CC2C1=O.Cl
Reaction #548509
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C1C2CCNCC2C(=O)N1Cc1ccccc1
Reaction #799648
title compound
Rendimiento 61.3%DOI: 10.6084/m9.figshare.5104873.v1
c1ccc(CN2CC3CCNCC3C2)cc1
Reaction #799649
title compound
Rendimiento 25.4%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CC2(C(=O)N[C@@H](Cc3ccc(N4C(=O)C5CCNCC5C4=O)cc3)C(=O)O)CCCC2)cc1
Reaction #1369793
N-[[1-[(4-methoxyphenyl)methyl]cyclopentyl]carbonyl]-4-[(3aRS,7aRS)-(octahydro-1,3-dioxo-1H-pyrrolo[3,4-c]pyridin-2-yl)]-L-phenylalanine
Rendimiento 13.8%DOI: 10.6084/m9.figshare.5104873.v1
Cl
Reaction #1502295
hydrogen chloride
DOI: 10.6084/m9.figshare.5104873.v1
O=C(NO)c1cc2c(CN3CC[C@@H]4C(=O)NC[C@@H]4C3)cn(Cc3ccc(F)cc3F)c2cn1
Reaction #2464235
title compound
Rendimiento 35.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(O)C(=O)c1cc2c(CN3CC[C@@H]4C(=O)NC[C@@H]4C3)cn(Cc3ccc(F)cc3F)c2cn1
Reaction #2464236
title compound
DOI: 10.6084/m9.figshare.5104873.v1