Busqueda de Subestructura

Cl.O=C1Nc2ccccc2CN1C1CCNCC1

O=C(CN1CCC(N2Cc3ccccc3NC2=O)CC1)c1cccc(Cl)c1
Reaction #95353
desired product
Rendimiento 50.4%DOI: 10.6084/m9.figshare.5104873.v1
O=C(CN1CCC(N2Cc3ccccc3NC2=O)CC1)c1ccc(Cl)cc1
Reaction #95354
desired product
Rendimiento 56.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C(=O)CN2CCC(N3Cc4ccccc4NC3=O)CC2)cc1
Reaction #95355
desired product
Rendimiento 66.9%DOI: 10.6084/m9.figshare.5104873.v1
O=C1Nc2ccccc2CN1C1CCN(CC(O)c2cccc(Cl)c2)CC1
Reaction #95357
desired product
Rendimiento 57.7%DOI: 10.6084/m9.figshare.5104873.v1
O=C1Nc2ccccc2CN1C1CCN(CC(O)c2ccc(Cl)cc2)CC1
Reaction #95358
desired product
Rendimiento 58.6%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(CC(=O)N1CCC(N2Cc3cc(O)ccc3NC2=O)CC1)Cc1cc(Cl)c(N)c(C(F)(F)F)c1
Reaction #173009
DOI: 10.1039/C8SC04228D
CN1CCN(C2CCN(C(=O)C(CC(=O)N3CCC(N4Cc5ccccc5NC4=O)CC3)Cc3cc(Cl)c(N)c(C(F)(F)F)c3)CC2)CC1
Reaction #180969
DOI: 10.1039/C8SC04228D
COCCN1Cc2c(cc(Br)c3[nH]ncc23)CC(CC(=O)N2CCC(c3cc4ccccc4[nH]c3=O)CC2)C1=O
Reaction #197301
DOI: 10.1039/C8SC04228D
Cc1cc2c(c3cn[nH]c13)CN(C)C(=O)C(NC(=O)N1CCC(N3Cc4ccccc4NC3=O)CC1)C2
Reaction #219437
4-(2-Oxo-1,4-dihydro-2H-quinazolin-3-yl)-piperidine-1-carboxylic acid (4,9-dimethyl-8-oxo-3,6,7,8,9,10-hexahydro-2,3,9-triaza-cyclohepta[e]inden-7-yl)-amide
DOI: 10.6084/m9.figshare.5104873.v1
CN1Cc2c(cc(Cl)c(O)c2Cl)CC(NC(=O)N2CCC(N3Cc4ccccc4NC3=O)CC2)C1=O
Reaction #219439
4-(2-Oxo-1,4-dihydro-2H-quinazolin-3-yl)-piperidine-1-carboxylic acid (7,9-dichloro-8-hydroxy-2-methyl-3-oxo-2,3,4,5-tetrahydro-1H-benzo[c]azepin-4-yl)-amide
Rendimiento 58.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(C[C@@H]1Cc2cc(Cl)c3[nH]ncc3c2CN(Cc2ccncc2)C1=O)N1CCC(c2cc(-c3ccccc3)[nH]n2)CC1
Reaction #219440
Title compound
Rendimiento 38.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)CN1Cc2c(cc(Cl)c3[nH]ncc23)C[C@@H](CC(=O)N2CCC(N3Cc4ccccc4CC3=O)CC2)C1=O
Reaction #219442
Title compound
Rendimiento 35.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)CN1Cc2c(cc(Cl)c3[nH]ncc23)C[C@@H](CC(=O)N2CCC(c3cc4ccccc4[nH]c3=O)CC2)C1=O
Reaction #219443
Title compound
Rendimiento 46.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)CN1Cc2c(cc(Cl)c3[nH]ncc23)C[C@@H](CC(=O)N2CCC(n3cc(-c4ccccc4)[nH]c3=O)CC2)C1=O
Reaction #219444
Title compound
Rendimiento 46.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)CN1Cc2c(cc(Cl)c3[nH]ncc23)C[C@@H](CC(=O)N2CCC(n3cc(-c4ccccn4)[nH]c3=O)CC2)C1=O
Reaction #219445
Title compound
Rendimiento 37.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)CN1Cc2c(cc(Cl)c3[nH]ncc23)C[C@@H](CC(=O)N2CCC(c3cc4cccc(F)c4[nH]c3=O)CC2)C1=O
Reaction #219446
Title compound
Rendimiento 36.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)CN1Cc2c(cc(Cl)c3[nH]ncc23)C[C@@H](CC(=O)N2CCC(c3nc4ccccc4[nH]c3=O)CC2)C1=O
Reaction #219447
Title compound
Rendimiento 49.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(C[C@@H]1Cc2cc(Cl)c3[nH]ncc3c2CN(Cc2ccncc2)C1=O)N1CCC(N2Cc3ccccc3NC2=O)CC1
Reaction #219448
Title compound
Rendimiento 27.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(C[C@@H]1Cc2cc(Cl)c3[nH]ncc3c2CN(Cc2ccncc2)C1=O)N1CCC(N2Cc3cccc(F)c3NC2=O)CC1
Reaction #219449
Title compound
Rendimiento 16.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(C[C@@H]1Cc2cc(Cl)c3[nH]ncc3c2CN(Cc2ccncc2)C1=O)N1CCC(c2cc3cccc(F)c3[nH]c2=O)CC1
Reaction #219450
Title compound
Rendimiento 13.0%DOI: 10.6084/m9.figshare.5104873.v1
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