Recherche de Sous-structure

CC(CCN)O

CCCO[C@H]1CN[C@@H]([C@@H](O)[C@H](Cc2cc(F)cc(F)c2)NC(=O)c2cccc(C(=O)NC(C)c3ccc(F)cc3)c2)C1
Reaction #49248
title compound
Rendement 84.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCO[C@H]1CN[C@@H]([C@@H](O)[C@H](Cc2cc(F)cc(F)c2)NC(=O)c2cccc(C(=O)NC(C)c3ccc(F)cc3)c2)C1
Reaction #49249
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NC1CCN(CC(c2ccc(Cl)c(Cl)c2)C2(O)CCCCC2)CC1
Reaction #57084
tert-butyl {1-[2-(3,4-dichlorophenyl)-2-(1-hydroxycyclohexyl)ethyl]piperidin-4-yl}carbamate
Rendement 53.0%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
O=S(=O)(Nc1ccccc1OC1CCN(c2nc3ccc(Br)cc3s2)CC1)c1ccccn1
Reaction #171353
Compound 27
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cccc(OC2CCN(S(C)(=O)=O)CCC2O)c1C
Reaction #174585
DOI: 10.1039/C8SC04228D
COC(=O)c1cccc(C(=O)NC(CC(=O)N2CCC(O)(c3ccc(Cl)cc3)C(C)(C)C2)C(C)C)c1
Reaction #177093
DOI: 10.1039/C8SC04228D
O=C(NCC(=O)N1CCC(Oc2cc(C(F)(F)F)ccc2F)CC1)c1cc(-c2ccccc2)[nH]n1
Reaction #184045
DOI: 10.1039/C8SC04228D
COc1ccc(COC(c2ccccc2)(c2ccc(OC)cc2)C2CNCC2O)cc1
Reaction #185205
DOI: 10.1039/C8SC04228D
CC(C)N(C)C1CCC(N2CCC(N)C2=O)C(C(C)(C)O)C1
Reaction #185507
DOI: 10.1039/C8SC04228D
NC1C(=O)N(CC2CC2)c2ccccc2OC1c1ccccc1
Reaction #186038
DOI: 10.1039/C8SC04228D
O=C(NCC(=O)N1CCC(Oc2cncc(C(F)(F)F)c2)CC1)c1cc(-c2ccccc2)[nH]n1
Reaction #188840
DOI: 10.1039/C8SC04228D
O=C(NCC(=O)N1CCC(Oc2cccc(C(F)(F)F)c2)CC1)c1cc(-c2cccc(O)c2)[nH]n1
Reaction #200670
DOI: 10.1039/C8SC04228D
CC(=O)c1cccc(OC(CCN2CCC(c3ccc(C)c(NC(=O)C(C)C)c3)CC2)c2ccccc2)c1
Reaction #202957
DOI: 10.1039/C8SC04228D
CC(C)c1nc(C(=O)N2CCOC3(CCN(Cc4cccc(C(F)C=O)c4)CC3)C2)cs1
Reaction #206578
DOI: 10.1039/C8SC04228D
COC1CC(C(=O)O)N(C(=O)CCCS)C1
Reaction #206655
DOI: 10.1039/C8SC04228D
CC1CN(CCC(O)c2ccccc2)CCC1(C)c1cccc(-c2c[nH]nn2)c1
Reaction #207562
DOI: 10.1039/C8SC04228D
CC[C@@H](C)[C@@]1(NC(C)=O)CCN([C@@H](CCc2ccccc2)C(=O)N[C@@H](Cc2cc(F)cc(F)c2)[C@H](O)[C@H]2C[C@H](Oc3ccccc3)CN2)C1=O
Reaction #220133
title compound
Rendement 73.0%DOI: 10.6084/m9.figshare.5104873.v1
CC[C@@H](C)[C@@]1(NC(C)=O)CCN([C@@H](CCc2ccccc2)C(=O)N[C@@H](Cc2cc(F)cc(F)c2)[C@H](O)[C@H]2C[C@H](Oc3ccccc3)CN2)C1=O
Reaction #220134
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC[C@@H](C)[C@@]1(NC(C)=O)CCN([C@@H](CCc2ccccc2)C(=O)N[C@@H](Cc2cc(F)cc(F)c2)[C@H](O)[C@H]2C[C@H](Oc3ccccn3)CN2)C1=O
Reaction #220136
title compound
Rendement 61.0%DOI: 10.6084/m9.figshare.5104873.v1
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