Busqueda de Subestructura

40336

COc1cc(CCc2cc(NC(=O)c3cnc(N4CCN5CCCCC5C4)nc3)[nH]n2)cc(OC)c1
Reaction #45109
title compound
Rendimiento 42.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(CCc2cc(NC(=O)c3cnc(N4CCN(C)C(C)C4)nc3)[nH]n2)cc(OC)c1
Reaction #45114
title compound
Rendimiento 36.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(CCc2cc(NC(=O)c3cnc(N4C[C@@H](C)N(C)[C@@H](C)C4)nc3)[nH]n2)cc(OC)c1
Reaction #45115
title compound
Rendimiento 39.4%DOI: 10.6084/m9.figshare.5104873.v1
CCN1CCN(c2ncc(C(=O)Nc3cc(CCc4cc(OC)cc(OC)c4)n[nH]3)cn2)CC1C
Reaction #45124
title compound
Rendimiento 49.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(CCc2cc(NC(=O)c3cnc(N4CCN(C)C(=O)C4)nc3)[nH]n2)cc(OC)c1
Reaction #45132
title compound
Rendimiento 45.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C(=O)Nc1ccc(-c2nn(C)cc2-c2ccnc3[nH]c(-c4cnc(N5CCNCC5)nc4)cc23)cc1
Reaction #57185
title compound
Rendimiento 43.0%DOI: 10.6084/m9.figshare.5104873.v1
Cn1cc(-c2ccnc3[nH]c(-c4cnc(N5CCN(C(=O)OC(C)(C)C)CC5)nc4)cc23)c(-c2ccc(N)cc2)n1
Reaction #57286
title product
Rendimiento 99.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C(=O)Nc1ccc(-c2nn(C)cc2-c2ccnc3[nH]c(-c4cnc(N5CCN(C(=O)OC(C)(C)C)CC5)nc4)cc23)cc1
Reaction #57287
title product
Rendimiento 27.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(c2ncc(-c3cc4c(-c5cn(C)nc5-c5ccc([N+](=O)[O-])cc5)ccnc4n3S(=O)(=O)c3ccccc3)cn2)CC1
Reaction #57288
title compound
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cnc(N2CCN(c3nnc(Cc4ccccc4)c4ccccc34)CC2)nc1
Reaction #70463
2-[4-(4-Benzyl-phthalazin-1-yl)-piperazin-1-yl]-pyrimidine-5-carbonitrile
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Nc1cnc(N2CCN(c3nnc(Cc4ccccc4)c4ccccc34)CC2)nc1
Reaction #70493
title compound
Rendimiento 31.9%DOI: 10.6084/m9.figshare.5104873.v1
CC[C@@H]1C(=O)N(C)c2cnc(N3CCN(C)CC3)nc2N1C1CCCC1
Reaction #73156
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(SCc2cnc(NC(=O)c3ccc(C(C)(C)C)cc3)s2)cc1C(=O)N1CCN(c2ncccn2)CC1
Reaction #77423
desired product
Rendimiento 63.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C([C@H]1CCCO1)N1CC[C@@H](Nc2nc(N3CCN(c4ccc(Cl)cc4)CC3)nc3c2S(=O)CC3)C1
Reaction #157298
((R)-3-{2-[4-(4-chloro-phenyl)-piperazin-1-yl]-5-oxo-6,7-dihydro-5H-5λ4-thieno[3,2-d]pyrimidin-4-ylamino}-pyrrolidin-1-yl)-(R)-tetrahydro-furan-2-yl-methanone
DOI: 10.6084/m9.figshare.5104873.v1
CC(Nc1cc(-c2cc3nccn3c(N3CC4CC3CN4C)n2)ccn1)c1ccccc1
Reaction #173793
DOI: 10.1039/C8SC04228D
CC(=O)Nc1c(N2CCOCC2)nc(N2CCN(c3ccccc3)CC2)nc1N1CCOCC1
Reaction #181665
DOI: 10.1039/C8SC04228D
CN(c1ccccc1)c1ncnc2c(N3CCOCC3)nc(N3CCNCC3)nc12
Reaction #188478
DOI: 10.1039/C8SC04228D
CONC(=O)c1cc(N2CCC(NC(=O)c3[nH]c(C)c(Cl)c3Cl)CC2)nc(N2CCNCC2)n1
Reaction #188753
DOI: 10.1039/C8SC04228D
CCCSc1nnc(C(=O)N2CCN(c3nc(N)c4cc(OC)c(OC)cc4n3)CC2)o1
Reaction #193131
DOI: 10.1039/C8SC04228D
O=S(=O)(c1ccccc1)N1CCN(c2ncc(Br)cn2)CC1
Reaction #193874
DOI: 10.1039/C8SC04228D
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