Substructure Search

1807

COc1c(CCN2CCN(c3cccc4nc(C)ccc34)CC2)cccc1N1CCNC1=O.Cl.Cl
Reaction #44144
title compound
Yield 38.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2c(N3CCN(CCc4cccc(N5C(=O)NC6CCCCC65)c4)CC3)cccc2n1
Reaction #44168
title compound
Yield 100.0%DOI: 10.6084/m9.figshare.5104873.v1
NCCCC1(CS(=O)(=O)N2CCC(Oc3ccc(Cl)cn3)CC2)NC(=O)NC1=O.O=C(O)C(F)(F)F
Reaction #60659
title compound
Yield 93.0%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)NCCCC1(CS(=O)(=O)N2CCC(Oc3ccc(Cl)cn3)CC2)NC(=O)NC1=O
Reaction #60660
N-{3-{4-[({4-[(5-chloropyridin-2-yl)oxy]piperidin-1-yl}sulfonyl}methyl]-2,5-dioxoimidazolidin-4-yl}propyl)methanesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CNc2nc(NCc3ccc(OC)cc3)nc(NN3CC(=O)NC3=O)n2)cc1
Reaction #163514
solid
Yield 43.1%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CNc2nc(Cl)nc(NN3CC(=O)NC3=O)n2)cc1
Reaction #163522
expected compound
Yield 66.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccncc1N1CCN(c2ccc(C(O)C(F)(F)F)c(F)c2)C1=O
Reaction #167388
product
Yield 65.9%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccncc1N1CCN(c2ccc3c(C(F)(F)F)n[nH]c3c2)C1=O
Reaction #167389
product
Yield 23.5%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccncc1N1CCN(c2ccc(C(O)C(F)(F)F)c(F)c2)C1=O
Reaction #167445
product
Yield 65.9%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccncc1N1CCN(c2ccc(C(=O)C(F)(F)F)c(F)c2)C1=O
Reaction #167446
product
Yield 74.5%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccncc1N1CCN(c2ccc3c(C(F)(F)F)n[nH]c3c2)C1=O
Reaction #167447
product
Yield 23.5%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CN(Cc2ccc(OC)cc2)S(=O)(=O)CCCN2CC(c3cccc(C(F)(F)F)c3)N(c3ccc(Oc4ccc(Cl)cc4)cc3)C2=O)cc1
Reaction #173932
DOI: 10.1039/C8SC04228D
Cc1ccc(C)c(N2CCN(C(=O)C3CN(S(=O)(=O)CCC(F)(F)F)C(=O)N3c3ccccc3)CC2)c1
Reaction #176415
DOI: 10.1039/C8SC04228D
Cl
Reaction #180208
DOI: 10.1039/C8SC04228D
CC(C)CC(C(=O)NN1C(=O)NC2(CCN(C)CC2)C1=O)C(CCCc1ccccc1)C(=O)OC(C)(C)C
Reaction #183037
DOI: 10.1039/C8SC04228D
CC(NC(Cc1ccccc1)C(=O)OCc1ccccc1)C(=O)N1C(=O)N(Cc2ccccc2)CC1C(=O)O
Reaction #184699
DOI: 10.1039/C8SC04228D
COc1cc2c(Oc3ccc(N4C(=O)CN(Cc5ccccc5)C4=O)cc3F)ccnc2cc1OCc1ccccc1
Reaction #189339
DOI: 10.1039/C8SC04228D
Cc1ccc(CN2C(=O)NC(CCO[Si](c3ccccc3)(c3ccccc3)C(C)(C)C)C2=O)cc1
Reaction #194314
DOI: 10.1039/C8SC04228D
N#Cc1ccc(N2C(=O)NC(=Cc3ccc(O)cc3)C2=O)c2ccccc12
Reaction #195925
DOI: 10.1039/C8SC04228D
CC1CCN(CC(=O)Nc2cc(N3C(=O)N(Cc4ccncc4)C(C)(C)C3=O)ccc2OC(F)(F)F)CC1
Reaction #198890
DOI: 10.1039/C8SC04228D
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