Recherche de Sous-structure

1366402

O=C(NC(CCNCCc1ccccn1)c1ccccc1)C1SCCN1S(=O)(=O)c1ccc(-c2ccccc2)cc1
Reaction #257942
DOI: 10.1039/C8SC04228D
O=C(NC(CCN1C(=O)c2ccccc2C1=O)c1ccccc1)C1SCCN1S(=O)(=O)c1ccc(-c2ccccc2)cc1
Reaction #283007
DOI: 10.1039/C8SC04228D
O=C(NC(CCOc1ccccc1)c1ccccc1)C1SCCN1S(=O)(=O)c1ccc(-c2ccccc2)cc1
Reaction #283203
DOI: 10.1039/C8SC04228D
O=C(NC(CCNCc1ccccc1)c1ccccc1)C1SCCN1S(=O)(=O)c1ccc(-c2ccccc2)cc1
Reaction #298046
DOI: 10.1039/C8SC04228D
O=C(NC(CCN1CCCCC1)c1ccccc1)C1SCCN1S(=O)(=O)c1ccc(-c2ccccc2)cc1
Reaction #392876
DOI: 10.1039/C8SC04228D
CN(CCC(NC(=O)C1SCCN1S(=O)(=O)c1ccc(-c2ccccc2)cc1)c1ccccc1)Cc1ccco1
Reaction #395255
DOI: 10.1039/C8SC04228D
O=C(NC(CCO)c1ccc(F)cc1)C1SCCN1S(=O)(=O)c1ccc(-c2ccccc2)cc1
Reaction #753787
DOI: 10.1039/C8SC04228D
O=C(NC(CCN1CCCC1)c1ccccc1)C1SCCN1S(=O)(=O)c1ccc(-c2ccccc2)cc1
Reaction #769697
DOI: 10.1039/C8SC04228D
CC(C)C(N)C(=O)OCCC(NC(=O)C1SCCN1S(=O)(=O)c1ccc(-c2ccccc2F)cc1)c1c(F)cccc1F
Reaction #770771
DOI: 10.1039/C8SC04228D
O=C(NC(CCO)c1ccccc1Cl)C1SCCN1S(=O)(=O)c1ccc(-c2ccccc2)cc1
Reaction #899200
DOI: 10.1039/C8SC04228D
CN(CCO)CCC(NC(=O)C1SCCN1S(=O)(=O)c1ccc(-c2ccccc2)cc1)c1ccccc1
Reaction #901896
DOI: 10.1039/C8SC04228D
O=C(NC(CCN1CCCCCC1)c1ccccc1)C1SCCN1S(=O)(=O)c1ccc(-c2ccccc2)cc1
Reaction #1310513
DOI: 10.1039/C8SC04228D
O=C(NC(CCN1C(=O)c2ccccc2C1=O)c1ccccc1)C1SCCN1S(=O)(=O)c1ccc(-c2ccccc2)cc1
Reaction #2051988
3-([1,1′-biphenyl]-4-ylsulfonyl)-N-[3-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)-1-phenylpropyl]-1,3-thiazolidine-2-carboxamide
Rendement 57.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NC(CCO)c1ccc(F)cc1)C1SCCN1S(=O)(=O)c1ccc(-c2ccccc2)cc1
Reaction #2051995
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(NC(CCO)c1ccccc1Cl)C1SCCN1S(=O)(=O)c1ccc(-c2ccccc2)cc1
Reaction #2051996
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(NC(CCO)c1ccc2c(c1)OCO2)C1SCCN1S(=O)(=O)c1ccc(-c2ccccc2)cc1
Reaction #2051997
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CN(CC[C@H](NC(=O)[C@@H]1SCCN1S(=O)(=O)c1ccc(-c2ccccc2)cc1)c1ccccc1)Cc1ccco1
Reaction #2051999
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CN(CCO)CC[C@H](NC(=O)[C@@H]1SCCN1S(=O)(=O)c1ccc(-c2ccccc2)cc1)c1ccccc1
Reaction #2052000
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CN(C)CC[C@H](NC(=O)[C@@H]1SCCN1S(=O)(=O)c1ccc(-c2ccccc2)cc1)c1ccccc1
Reaction #2052001
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(NC(CCN1CCCC1)c1ccccc1)C1SCCN1S(=O)(=O)c1ccc(-c2ccccc2)cc1
Reaction #2052002
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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