Busqueda de Subestructura

8511

CN(C(Cc1ccc(OCc2ccccc2)c(OCc2ccccc2)c1)CN1CCN(c2ccccc2)CC1)S(=O)(=O)c1cccc2cnccc12
Reaction #5815
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(c1cccc2cnccc12)N1Cc2cc(O)c(O)cc2CC1CN1CCN(c2ccccc2)CC1
Reaction #5816
title compound
Rendimiento 90.9%DOI: 10.6084/m9.figshare.5104873.v1
O=C([C@H](Cc1ccc(OS(=O)(=O)c2cccc3cnccc23)cc1)NS(=O)(=O)c1cccc2cnccc12)N1CCN(CCCc2ccccc2)CC1
Reaction #5818
title compound
Rendimiento 60.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C([C@H](Cc1ccc(O)cc1)NS(=O)(=O)c1cccc2cnccc12)N1CCN(CCCc2ccccc2)CC1
Reaction #5819
title compound
Rendimiento 46.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(OCc1ccccc1)N1CCCN(C(=O)[C@H](Cc2ccc(O)cc2)NS(=O)(=O)c2cccc3cnccc23)CC1
Reaction #5827
title compound
Rendimiento 74.7%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CC(CN2CCC(=O)CC2)N(C)S(=O)(=O)c2cccc3cnccc23)cc1
Reaction #5828
N-{1-(p-methoxybenzyl)-2-(4-oxopiperidino)ethyl}-N-methyl-5-isoquinolinesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1
CC(=Cc1ccc(Cl)cc1)CNCCNS(=O)(=O)c1cccc2cnccc12
Reaction #5835
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(NCCNCC=Cc1ccc(Cl)cc1)c1cccc2cnccc12
Reaction #5836
title compound
Rendimiento 71.5%DOI: 10.6084/m9.figshare.5104873.v1
CN(CC=Cc1ccc(Cl)cc1)CCNS(=O)(=O)c1cccc2cnccc12
Reaction #5837
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(c1cccc2cnccc12)N1CCN(CC=Cc2ccc(Cl)cc2)CC1
Reaction #5838
title compound
Rendimiento 25.5%DOI: 10.6084/m9.figshare.5104873.v1
O=CN(CC=Cc1ccc(Cl)cc1)CCNS(=O)(=O)c1cccc2cnccc12
Reaction #5839
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(NCCN(CC=Cc1ccc(Cl)cc1)Cc1ccc(O)cc1)c1cccc2cnccc12
Reaction #5840
title compound
Rendimiento 59.3%DOI: 10.6084/m9.figshare.5104873.v1
CN(CC=Cc1ccc(Cl)cc1)CCN(CCN1CCCCC1)S(=O)(=O)c1cccc2cnccc12
Reaction #5841
title compound
Rendimiento 74.9%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(S(=O)(=O)c2cccc3c2CCNC3)CC1
Reaction #8815
5-(4-methyl-piperazine-1-sulfonyl)-1,2,3,4-tetrahydro-isoquinoline
Rendimiento 124.1%DOI: 10.6084/m9.figshare.5104873.v1
Cl.NCCN(CCS(=O)(=O)c1ccccc1)S(=O)(=O)c1cccc2c(N)nccc12
Reaction #10596
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1CN(S(=O)(=O)c2cccc3cnccc23)C(C)CN1
Reaction #173072
DOI: 10.1039/C8SC04228D
CCCCCCN(CCN1CCCCC1)S(=O)(=O)c1cccc2cnccc12
Reaction #195193
DOI: 10.1039/C8SC04228D
CN(CCN(CCOc1ccccc1Cc1ccccc1)C(=O)OC(C)(C)C)S(=O)(=O)c1cccc2cnccc12
Reaction #207956
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)NCCNS(=O)(=O)c1cc(-c2ccccc2)cc2cnccc12
Reaction #223374
DOI: 10.1039/C8SC04228D
CN(C(Cc1ccc(O)cc1)CN1CCCN(C(=O)OCc2ccccc2)CC1)S(=O)(=O)c1cccc2cnccc12
Reaction #229595
DOI: 10.1039/C8SC04228D
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