Busqueda de Subestructura

C1CCC(CC1)N

Cl.Cl.OC(NC1CCCCC1)=[SH]CCCN1CCN(CCc2ccc(Cl)cc2)CC1
Reaction #3931
N-cyclohexyl-S-{3-[4-(4-chlorophenethyl)piperazin-1-yl]propyl}thiocarbamate dihydrochloride
Rendimiento 170.7%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)c1ncc(C(=O)O)c(O[C@H]2CC[C@H](NC(=O)OC(C)(C)C)CC2)n1
Reaction #51222
N-tert-butoxycarbonyl-trans-4-[5-carboxy-2-(dimethylamino)pyrimidin-4-yloxy]cyclohexylamine
Rendimiento 80.9%DOI: 10.6084/m9.figshare.5104873.v1
N#CC1(NC(=O)C(CC2CCCCC2)NC2=NS(=O)(=O)c3ccccc32)CCN(C2CCCCC2)C1
Reaction #53528
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc([C@H]2CC[C@H](NC(=O)OCc3ccccc3)CC2)cc1
Reaction #56668
trans-Ethyl 4-(4-(N-benzyloxycarbonylamino)cyclohexyl)benzoate
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)O[C@H]1C[C@@H]2CC[C@@H]3[C@H](CC[C@]4(C)C(=O)[C@@H](N5CCCCC5)C[C@@H]34)[C@@]2(C)C[C@@H]1N1CCCCC1
Reaction #65119
(2β,3α,5α,16β)-3-acetyloxy-2,16-di-(1-piperidinyl)androstan-17-one
DOI: 10.6084/m9.figshare.5104873.v1
O=C1C=C(NC2CCCCC2)C(c2ccc(N3CCOCC3)cc2)N1c1ccc2[nH]cnc2c1
Reaction #70049
1-(1H-Benzo[d]imidazol-5-yl)-4-(cyclohexylamino)-5-(4-morpholinophenyl)-1H-pyrrol-2(5H)-one
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cccc([C@H]2CC[C@H](NC(=O)c3nc(Cl)c(CC)[nH]3)CC2)c1
Reaction #72106
title compound
Rendimiento 53.0%DOI: 10.6084/m9.figshare.5104873.v1
CCc1[nH]c(C(=O)N[C@H]2CC[C@H](c3cccc(C(=O)O)c3)CC2)nc1Cl
Reaction #72107
title compound
Rendimiento 58.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cccc([C@H]2CC[C@@H](NC(=O)c3nc(Cl)c(CC)[nH]3)CC2)c1
Reaction #72108
title compound
Rendimiento 53.8%DOI: 10.6084/m9.figshare.5104873.v1
CCc1[nH]c(C(=O)N[C@H]2CC[C@@H](c3cccc(C(=O)O)c3)CC2)nc1Cl
Reaction #72109
title compound
Rendimiento 49.4%DOI: 10.6084/m9.figshare.5104873.v1
c1cc(-c2c[nH]c([C@@H]3CC4CCCCC4N3)n2)ccc1-c1ccc(-c2c[nH]c([C@H]3NC4CCC3C4)n2)cc1
Reaction #162867
(2S)-2-(4-(4′-(2-((3S)-2-azabicyclo[2.2.1]heptan-3-yl)-1H-imidazol-4-yl)biphenyl-4-yl)-1H-imidazol-2-yl)octahydro-1H-indole
DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)[C@@H]1CC[C@]2(NCCN3CCS(=O)(=O)CC3)CC[C@]3(C)[C@H](CC[C@@H]4[C@@]5(C)CC=C(c6ccc(C(=O)O[C@H]7O[C@H](C(=O)OCc8ccccc8)[C@@H](O)[C@H](O)[C@H]7O)cc6)C(C)(C)[C@@H]5CC[C@]43C)[C@@H]12
Reaction #172892
desired product
Rendimiento 14.4%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)[C@@H]1CC[C@]2(NCCN3CCS(=O)(=O)CC3)CC[C@]3(C)[C@H](CC[C@@H]4[C@@]5(C)CC=C(c6ccc(C(=O)O[C@H]7O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]7O)cc6)C(C)(C)[C@@H]5CC[C@]43C)[C@@H]12
Reaction #172893
desired product
Rendimiento 52.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)NC1CC(NC(C)(C)C)CCC1N1CCC(NC(=O)OCc2ccccc2)C1=O
Reaction #175812
DOI: 10.1039/C8SC04228D
c1ccc2c(C3CCC(N4CCN(c5cccc6[nH]ccc56)CC4)CC3)c[nH]c2c1
Reaction #176321
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)NC1CCN(C2CCCCC2OCc2ccccc2)C1
Reaction #180053
DOI: 10.1039/C8SC04228D
Oc1ccc(C2CCC(NCCCc3ccccc3)CC2)cc1
Reaction #180726
DOI: 10.1039/C8SC04228D
[Br-]
Reaction #187241
DOI: 10.1039/C8SC04228D
Oc1cccc(C2CNC3(CCCCC3)O2)c1
Reaction #206037
DOI: 10.1039/C8SC04228D
O=C(CNC(=O)c1cccc(C(F)(F)F)c1)NC1CN(C2CCC(NC(=O)c3ccc4c(c3)OCO4)CC2)C1
Reaction #206616
DOI: 10.1039/C8SC04228D
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