Busqueda de Subestructura

1331027

O=C(CCl)NCc1cccc2c1C(=O)N(C1CCC(=O)NC1=O)C2=O
Reaction #10054
product
Rendimiento 84.0%DOI: 10.6084/m9.figshare.5104873.v1
[N-]=[N+]=NCC(=O)NCc1cccc2c1C(=O)N(C1CCC(=O)NC1=O)C2=O
Reaction #10064
2-azido-N-{[2-(2,6-dioxo(3-piperidyl))-1,3-dioxoisoindolin-4-yl]methyl}acetamide
Rendimiento 90.8%DOI: 10.6084/m9.figshare.5104873.v1
[N-]=[N+]=NCC(=O)Nc1cccc2c1C(=O)N(C1CCC(=O)NC1=O)C2=O
Reaction #10083
product
Rendimiento 96.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CN(Cc2ccc(F)cc2)CCN1C(=O)CCl
Reaction #11721
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CN(Cc2ccc(F)cc2)CCN1C(=O)COc1ccc(Cl)cc1[N+](=O)[O-]
Reaction #11722
title compound
Rendimiento 94.8%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H]1CC[C@H](N(CCNC(=O)OC(C)(C)C)C(=O)CCl)CC1
Reaction #44985
methyl trans-4-[{2-[(t-butoxycarbonyl)amino]ethyl}-(chloroacetyl)amino]cyclohexanecarboxylate
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H]1CC[C@H](N2CCN(C(=O)OC(C)(C)C)CC2=O)CC1
Reaction #44986
t-butyl 4-[trans-4-(methoxycarbonyl)cyclohexyl]-3-oxopiperazine-1-carboxylate
Rendimiento 59.7%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #63576
20.6
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccccc1C1CCC(=O)C(Cl)C1
Reaction #81410
2-Chloro-4-(2-methylphenyl)cyclohexanone
DOI: 10.6084/m9.figshare.5104873.v1
CCCCC(CC)CN(CC(CC)CCCC)C(=O)C(Cl)c1ccccc1
Reaction #89797
2-chloro-N,N-bis(2-ethylhexyl)-2-phenyl-acetamide
Rendimiento 96.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCOc1ccc(F)c2c(=O)c(-c3ccc(OC)cc3)c[nH]c12.[NH-]CC(Cl)C(=O)O
Reaction #155349
5-fluoro-3-(4-methoxyphenyl)-4-oxo-8-propoxy-1,4-dihydroquinoline 2-carboxy-(2-chloroethyl)amide
Rendimiento 58.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCOc1ccc(F)c2c(=O)c(-c3ccc(OC)cc3)c[nH]c12.CN1CCN(C(C[NH-])C(=O)O)CC1
Reaction #155350
5-fluoro-3-(4-methoxyphenyl)-4-oxo-8-propoxy-1,4-dihydro-quinoline 2-carboxy-[2-(4-methylpiperazin-1-yl)ethyl]amide
Rendimiento 14.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C(CCl)NCC1(O)CCN(Cc2ccccc2)CC1
Reaction #166409
compound 398
Rendimiento 78.4%DOI: 10.6084/m9.figshare.5104873.v1
O=C1COC2(CCN(Cc3ccccc3)CC2)CN1
Reaction #166410
compound 399
Rendimiento 62.1%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CCC2(C3CCCC3)CC(O)=C(Sc3nnc(CN(C)C)n3C)C(=O)O2)cc1Cl
Reaction #180732
DOI: 10.1039/C8SC04228D
Cc1cccc(C)c1N(CC1OCCO1)C(=O)CCl
Reaction #182313
DOI: 10.1039/C8SC04228D
Cc1cc(C)n2nc(SC3=C(O)CC(CCNC(=O)CCc4ccco4)(C4CCCC4)OC3=O)nc2n1
Reaction #185359
DOI: 10.1039/C8SC04228D
CC(C)N1C(=O)CN(C(=O)c2ccccc2-c2ccc(C(F)(F)F)cc2)c2ccc(OCc3ccccc3)cc21
Reaction #187858
DOI: 10.1039/C8SC04228D
CCOC(=O)C(Cl)=Cc1cc(NC(=O)C2=C(C(N)=O)CCCC2)ccc1Cl
Reaction #188201
DOI: 10.1039/C8SC04228D
COc1ccc(CCC2(C3CCCC3)CC(O)=C(Sc3nc(C)cc(C)c3C#N)C(=O)O2)cc1Cl
Reaction #191196
DOI: 10.1039/C8SC04228D
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