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NC(=O)c1ccccc1

CC(=O)Nc1ccc(C(=O)N(CCN2CCC(C(=O)c3ccc(F)cc3)CC2)c2cccnc2)cc1
Reaction #2583
title compound
Ausbeute 95.6%DOI: 10.6084/m9.figshare.5104873.v1
COCCN(CCN1CCC(C(=O)c2ccc(F)cc2)CC1)C(=O)c1ccc(CNC(=O)[C@H](C)NC(=O)OC(C)(C)C)cc1
Reaction #2605
title compound
Ausbeute 72.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Nc1ccc(C(=O)N(CCN2CCC(C(=O)c3ccc(F)cc3)CC2)c2cccc(O)c2)cc1
Reaction #2612
title compound
Ausbeute 76.7%DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)Nc1ccc(C(=O)N(CCN2CCC(C(=O)c3ccc(F)cc3)CC2)c2cccnc2)cc1.NC(=O)Nc1ccc(C(=O)N(CCN2CCC(C(=O)c3ccc(F)cc3)CC2)c2cccnc2)cc1.O=C(O)/C=C/C(=O)O
Reaction #2630
title compound
Ausbeute 56.5%DOI: 10.6084/m9.figshare.5104873.v1
CCN(CC)CCNC(=O)c1ccc2[nH]c(-c3cc(-c4ccncc4)n[nH]c3=O)nc2c1
Reaction #40544
2-(3-Oxo-6-pyridin-4-yl-2,3-dihydropyridazin-4-yl)-1H-benzimidazole-5-carboxylic acid (2-diethylaminoethyl)amide
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ccc(-c2ccc(-c3ccc(NC(=O)c4ccccc4)cc3)o2)cc1)c1ccccc1
Reaction #47988
2,5-bis(4-benzamidophenyl)furan
Ausbeute 96.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCN(C)C(=O)c1cccc(C(=O)N[C@@H](Cc2cc(F)cc(F)c2)[C@H](O)[C@H]2C[C@@H](OCCC)CN2)c1
Reaction #49233
title compound
Ausbeute 80.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCO[C@H]1CN[C@@H]([C@@H](O)[C@H](Cc2cc(F)cc(F)c2)NC(=O)c2cccc(C(=O)N(CCC)CCC)c2)C1
Reaction #49234
title compound
Ausbeute 89.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCN(C)C(=O)c1cc(C)cc(C(=O)N[C@@H](Cc2cc(F)cc(F)c2)[C@H](O)[C@H]2C[C@@H](OCCC)CN2)c1
Reaction #49240
title compound
Ausbeute 85.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCO[C@H]1CN[C@@H]([C@@H](O)[C@H](Cc2cc(F)cc(F)c2)NC(=O)c2cc(C)cc(C(=O)N(CCC)CCC)c2)C1
Reaction #49241
title compound
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccccc1-c1ccc2c(c1)C(CN(C)C(=O)c1ccccc1)=CC(C)(C)N2
Reaction #54058
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)N1CCC(COCC(NC(=O)c2ccc3c(Cl)c[nH]c3c2)c2ccccc2F)CC1
Reaction #60711
title compound
Ausbeute 78.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)N1CCC(COCC(NC(=O)c2ccc3c(Cl)c[nH]c3c2)c2ccc(F)cc2)CC1
Reaction #60714
title compound
Ausbeute 76.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)N1CCC(CN(C)C[C@H](NC(=O)c2ccc3c(Cl)c[nH]c3c2)c2ccccc2)CC1
Reaction #60739
3-Chloro-N-{(R)-2-[(1-isopropylpiperidin-4-ylmethyl)-(methyl) amino]-1-phenylethyl}-1H-indole-6-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)c1ccc(N2CCN(C(=O)c3cc(C#N)ccc3N3CCOCC3)CC2)c(F)c1
Reaction #61002
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CN(C)c2ccc(OC)c3nc(NC(=O)c4ccc(F)cc4)sc23)cc1
Reaction #80162
4-Fluoro-N-{4-methoxy-7-[(4-methoxy-benzyl)-methyl-amino]-benzothiazol-2-yl}-benzamide
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(N(C)CC(=O)N2CCCCC2)c2sc(NC(=O)c3ccc(F)cc3)nc12
Reaction #80164
4-Fluoro-N-{4-methoxy-7-[methyl-(2-oxo-2-piperidin-1-yl-ethyl)-amino]-benzothiazol-2-yl}-benzamide
DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C1CCN(C(=O)c2ccc(-c3cnc(N)c(C(=O)Nc4ccccc4)n3)cc2)CC1
Reaction #165761
title compound
Ausbeute 80.0%DOI: 10.6084/m9.figshare.5104873.v1
CCNC(=O)c1cc2c(Oc3ccc(N)c(Cl)c3)ccnc2cc1OCc1ccccc1
Reaction #186593
DOI: 10.1039/C8SC04228D
CCCCCCc1ccc(-c2c(O)c(C(C)=NNC(=O)c3ccc(C(=O)O)cc3)nn2C)cc1
Reaction #190673
DOI: 10.1039/C8SC04228D
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