Recherche de Sous-structure

CCN(CC)CCNC

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
COc1ccccc1N(CCN1CCC(C(=O)c2ccc(F)cc2)CC1)C(=O)c1ccc(CNS(C)(=O)=O)cc1
Reaction #2600
title compound
Rendement 57.5%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccccc1N(CCN1CCC(C(=O)c2ccc(F)cc2)CC1)C(=O)c1ccc(NS(C)(=O)=O)cc1
Reaction #2601
title compound
Rendement 50.7%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
Rendement 71.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1ccccc1
Reaction #83384
benzoic acid
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
COC(=O)[C@H]1CN(/C(=N/C#N)N2CCCCC2)CC[C@@H]1C(=O)N1CCN(c2ccc(C#N)cc2C)CC1
Reaction #89764
methyl(3R,4S)-1-[(E)-(cyanoimino)(piperidin-1-yl)methyl]-4-[4-(4-cyano-2-methylphenyl)piperazin-1-yl]carbonylpiperidine-3-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(C#N)ccc1N1CCN(C(=O)[C@H]2CCN(/C(=N/C#N)N3CCCCC3)C[C@@H]2C(=O)NO)CC1
Reaction #89765
(3R,4S)-1-[(E)-(cyanoimino)(piperidin-1-yl)methyl]-4-[4-(4-cyano-2-methylphenyl)piperazin-1-yl]carbonyl-N-hydroxypiperidine-3-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NCCCCC(NC(=O)C(N)Cc1cc(Cl)c(O)c(Cl)c1)C(=O)N1CCN(c2ccncc2)CC1
Reaction #177823
DOI: 10.1039/C8SC04228D
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(C)(C)OC(=O)NCc1cc(Cl)c(NC(=O)CN2CCN(CCCCC(c3ccc(F)cc3)c3ccc(F)cc3)CC2C(N)=O)c(Cl)c1
Reaction #196096
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
CS(=O)(=O)Nc1ccc(-n2c(C(=O)N3CCC(F)(F)CC3)cc3cc(C(=O)N4CCN(C5CCC5)CC4)ccc32)cc1
Reaction #199337
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
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
CNC(=O)C1CN(CC(=O)Nc2c(Cl)cc(C(C)=O)cc2Cl)CCN1CCCCN(c1ccc(F)cc1)c1ccc(F)cc1
Reaction #208901
DOI: 10.1039/C8SC04228D
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