Recherche de Sous-structure

74762

Cc1ccc(-c2cnccc2C)c(C(=O)O)c1
Reaction #89183
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-c2cnccc2C)c(C(=O)N2CCC[C@@H](C)[C@H]2CNc2ccc(C(F)(F)F)cn2)c1
Reaction #89184
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-c2cccnc2)c(C(=O)O)c1
Reaction #89223
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-c2cccnc2)c(C(=O)N2CCC[C@@H](C)[C@H]2CNc2nc3cc(Cl)ccc3o2)c1
Reaction #89224
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-c2ccc(C)nc2)c(C(=O)O)c1
Reaction #89235
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-c2ccc(C)nc2)c(C(=O)N2CCC[C@@H](C)[C@H]2CNc2nc3cc(Cl)ccc3o2)c1
Reaction #89236
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1c(C)c(Cc2ccc(-c3cccnc3)c(C(=O)Nc3ccc(C(F)(F)F)cc3)c2)c(OC)c(OC)c1OC
Reaction #300494
DOI: 10.1039/C8SC04228D
COc1c(C)c(Cc2ccc(-c3cccnc3)c(C(=O)N3CCOCC3)c2)c(OC)c(OC)c1OC
Reaction #399546
DOI: 10.1039/C8SC04228D
COc1c(C)c(Cc2ccc(-c3cccnc3)c(C(=O)O)c2)c(OC)c(OC)c1OC
Reaction #754426
DOI: 10.1039/C8SC04228D
COC1=C(OC)C(=O)C(Cc2ccc(-c3cccnc3)c(C(=O)Nc3ccc(OC)cc3)c2)=C(C)C1=O
Reaction #1238097
DOI: 10.1039/C8SC04228D
COC(=O)c1cc(Cc2c(C)c(OC)c(OC)c(OC)c2OC)ccc1-c1cccnc1
Reaction #1332350
title compound
Rendement 98.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1c(C)c(Cc2ccc(-c3cccnc3)c(C(=O)O)c2)c(OC)c(OC)c1OC
Reaction #1332360
title compound
Rendement 88.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1c(C)c(Cc2ccc(-c3cccnc3)c(C(=O)N3CCCCC3)c2)c(OC)c(OC)c1OC
Reaction #1332370
title compound
Rendement 49.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1c(C)c(Cc2ccc(-c3cccnc3)c(C(=O)N3CCOCC3)c2)c(OC)c(OC)c1OC
Reaction #1332371
title compound
Rendement 55.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1c(C)c(Cc2ccc(-c3cccnc3)c(C(=O)Nc3ccc(C(F)(F)F)cc3)c2)c(OC)c(OC)c1OC
Reaction #1332372
title compound
Rendement 53.0%DOI: 10.6084/m9.figshare.5104873.v1
COC1=C(OC)C(=O)C(Cc2ccc(-c3cccnc3)c(C(=O)O)c2)=C(C)C1=O
Reaction #1332382
title compound
Rendement 58.1%DOI: 10.6084/m9.figshare.5104873.v1
COC1=C(OC)C(=O)C(Cc2ccc(-c3cccnc3)c(C(=O)N3CCOCC3)c2)=C(C)C1=O
Reaction #1332398
title compound
Rendement 68.0%DOI: 10.6084/m9.figshare.5104873.v1
COC1=C(OC)C(=O)C(Cc2ccc(-c3cccnc3)c(C(=O)Nc3ccc(OC)cc3)c2)=C(C)C1=O
Reaction #1332399
title compound
Rendement 36.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ncccc1-c1ccc(-c2nc(-c3ccc(Cl)c(Cl)c3)cs2)cc1C(=O)O
Reaction #1606521
5-[4-(3,4-dichloro-phenyl)-thiazol-2-yl]-2-(2-methoxy-pyridin-3-yl)-benzoic acid
Rendement 12.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ncccc1-c1ccc(-c2nc(-c3ccc(Cl)c(Cl)c3)cs2)cc1C(=O)O
Reaction #1606533
5-[4-(3,4-dichloro-phenyl)-thiazol-2-yl]-2-(2-methyl-pyridin-3-yl)-benzoic acid
Rendement 59.0%DOI: 10.6084/m9.figshare.5104873.v1
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