Substructure Search

CCN(CC)CC

CC(=O)Nc1ccc(C(=O)N(CCN2CCC(C(=O)c3ccc(F)cc3)CC2)c2ccccc2C(F)(F)F)cc1
Reaction #2581
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ccc(C(=O)N(CCN2CCC(C(=O)c3ccc(F)cc3)CC2)c2cccnc2)cc1)c1ccccc1
Reaction #2615
title compound
Yield 71.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)N1CCC(Oc2ccc3c(c2)cc(C(=O)N2CCC(F)(F)CC2)n3-c2cccc(OC(F)(F)F)c2)CC1
Reaction #48126
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)N1CCC(Oc2ccc3c(c2)cc(C(=O)N2CCC(F)(F)CC2)n3-c2ccc(Cl)c(Cl)c2)CC1
Reaction #48139
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1cc(CCc2cc(F)cc(F)c2NC(=O)NC2CCN(Cc3ccccc3)CC2)cc(C(C)(C)C)c1O.Cl
Reaction #82128
title compound
Yield 81.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1cc(CCc2cc(F)cc(F)c2NC(=O)NC2CCN(Cc3ccccc3)CC2)cc(C(C)(C)C)c1O.CS(=O)(=O)O
Reaction #82129
title compound
Yield 87.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-n2nccn2)c(C(=O)N2CCC[C@@H](C)[C@H]2CNc2ncc3ccccc3n2)c1
Reaction #89436
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-n2nccn2)c(C(=O)N2CCC[C@@H](C)[C@H]2CNc2ncc(C(F)(F)F)cn2)c1F
Reaction #89531
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CN2C(=O)CC[C@@H]2/C=C(\c2ccc(C(C)(C)C)cc2)c2ccc(N)c(OC)n2)c(OC)c1
Reaction #157828
(5R)-5-[(E)-2-(5-amino-6-methoxypyridin-2-yl)-2-(4-tert-butylphenyl)ethenyl]-1-(2,4-dimethoxybenzyl)pyrrolidin-2-one
DOI: 10.6084/m9.figshare.5104873.v1
COc1nc(/C(=C/[C@H]2CCC(=O)N2)c2ccc(C(C)(C)C)cc2)ccc1N
Reaction #157829
(5R)-5-[(E)-2-(5-amino-6-methoxypyridin-2-yl)-2-(4-tert-butylphenyl)ethenyl]pyrrolidin-2-one
Yield 44.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)c1ccc(CCNC(=O)C2CCN(C(=O)c3cc4ccccc4n3Cc3ccc(Cl)cc3)CC2)cc1
Reaction #170817
1-(1-(4-chlorobenzyl)-1H-indole-2-carbonyl)-N-(4-isopropylphenethyl)piperidine-4-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
Cl
Reaction #187513
DOI: 10.1039/C8SC04228D
CC(C)N1CCC(Oc2cc3cc(C(=O)N4CCN(C(=O)C5CC5)CC4)[nH]c3cc2Br)CC1
Reaction #188624
DOI: 10.1039/C8SC04228D
CC(=O)N1CCN(C(=O)c2cc3cc(OC4CCN(C(C)C)CC4)ccc3n2C(C)C)CC1
Reaction #190962
DOI: 10.1039/C8SC04228D
COc1cc(N2CCN(C(=O)Cn3nc(C(F)(F)F)c(Cl)c3-c3ccc(C(F)(F)F)cc3)CC2)ccc1Cl
Reaction #194841
DOI: 10.1039/C8SC04228D
CC(=O)Nc1ccc(CN2CCN(C(=O)c3cc(C(F)(F)F)cc(C(F)(F)F)c3)C(Cc3ccc(Cl)c(Cl)c3)C2)cc1
Reaction #196589
DOI: 10.1039/C8SC04228D
CCN(CC)C(=O)N1CCN(C(=O)c2cc3cc(OC4CCN(C(C)C)CC4)ccc3[nH]2)CC1
Reaction #199979
DOI: 10.1039/C8SC04228D
CC(CC(=O)N1CCC(O)(c2ccc(Cl)cc2)C(C)(C)C1)NC(=O)c1cccc(-c2nnn(COCc3ccccc3)n2)c1
Reaction #202668
DOI: 10.1039/C8SC04228D
COC(=O)NCC1CCC(C(=O)N2CC(c3ccc(F)cc3)C(N(C)C(=O)N(C)c3cc(C(F)(F)F)cc(C(F)(F)F)c3)C2)CC1
Reaction #205365
DOI: 10.1039/C8SC04228D
CC(C)N1CCC(Oc2ccc3c(c2)cc(C(=O)N2CCS(=O)(=O)CC2)n3C(C)C)CC1
Reaction #207138
DOI: 10.1039/C8SC04228D
Page 1Next