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1192816

NC(=O)c1cc2c(N3CCNCC3)cccc2o1
Reaction #313
Ausbeute 0.0%
N#Cc1ccc2[nH]cc(CCCCN3CCN(c4ccc5oc(C(N)=O)cc5c4)CC3)c2c1
Reaction #1264
1-[4-(5-cyanoindol-3-yl)butyl]-4-(2-carbamoylbenzofuran-5-yl)piperazine
DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)c1cc2cc(N3CCNCC3)ccc2o1
Reaction #1268
5-(1-piperazinyl)benzofuran-2-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1cccc(NCc2cc3ccccc3o2)c1C(=O)O
Reaction #10147
3-[(Benzofuran-2-ylmethyl)-amino]-phthalic acid
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(N)cc2cc(C(=O)N[C@H]3CN4CCC3CC4)oc12.Cl.Cl
Reaction #43733
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@H]1CN2CCC1CC2)c1cc2ccc([N+](=O)[O-])cc2o1
Reaction #43738
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc2cc(C(=O)N[C@H]3CN4CCC3CC4)oc2c1
Reaction #43739
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Nc1cccc2cc(C(=O)N[C@H]3CN4CCC3CC4)oc12
Reaction #43741
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H](NS(=O)(=O)c1ccc(-c2ccc(NC(=O)c3oc4cccc(OC)c4c3C)cc2)cc1)C(C)C
Reaction #57620
(S)-2-{4′-[(4-methoxy-3-methyl-benzofuran-2-carbonyl)-amino]-biphenyl-4-sulfonylamino}-3-methyl-butyric acid methyl ester
Ausbeute 33.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc2oc(C(=O)Nc3ccc(-c4ccc(S(=O)(=O)N[C@H](C(=O)O)C(C)C)cc4)cc3)c(C)c12
Reaction #57621
(S)-2-{4′-[(4-methoxy-3-methyl-benzofuran-2-carbonyl)-amino]-biphenyl-4-sulfonylamino}-3-methyl-butyric acid
Ausbeute 81.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOc1cccc2oc(C(=O)Nc3ccc(-c4ccc(S(=O)(=O)N[C@H](C(=O)O)C(C)C)cc4)cc3)c(C)c12
Reaction #57625
(S)-2-{4′-[(4-ethoxy-3-methyl-benzofuran-2-carbonyl)-amino]-biphenyl-4-sulfonylamino}-3-methyl-butyric acid
Ausbeute 91.3%DOI: 10.6084/m9.figshare.5104873.v1
CCCOc1cccc2oc(C(=O)Nc3ccc(-c4ccc(S(=O)(=O)N[C@H](C(=O)O)C(C)C)cc4)cc3)c(C)c12
Reaction #57629
(S)-3-methyl-2-{4′-[(3-methyl-4-propoxy-benzofuran-2-carbonyl)-amino]-biphenyl-4-sulfonylamino}-butyric acid
Ausbeute 86.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(C(=O)Nc2ccc(-c3ccc(S(=O)(=O)N[C@H](C(=O)O)C(C)C)cc3)cc2)oc2cccc(-c3cccnc3)c12
Reaction #57644
(S)-3-methyl-2-{4′-[(3-methyl-4-pyridin-3-yl-benzofuran-2-carbonyl)-amino]-biphenyl-4-sulfonylamino}-butyric acid
Ausbeute 76.8%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(C(=O)Nc2ccc(-c3ccc(S(=O)(=O)N[C@H](C(=O)O)C(C)C)cc3)cc2)oc2cccc(N3CCOCC3)c12
Reaction #57655
(S)-3-methyl-2-{4′-[(3-methyl-4-morpholin-4-yl-benzofuran-2-carbonyl)-amino]-biphenyl-4-sulfonylamino}-butyric acid
Ausbeute 96.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1c(Cl)ccc2oc(C(=O)Nc3ccc(-c4ccc(S(=O)(=O)N[C@H](C(=O)O)C(C)C)cc4)cc3)c(C)c12
Reaction #57665
(S)-2-{4′-[(5-chloro-4-methoxy-3-methyl-benzofuran-2-carbonyl)-amino]-biphenyl-4-sulfonylamino}-3-methyl-butyric acid
Ausbeute 62.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1c(Br)ccc2oc(C(=O)Nc3ccc(-c4ccc(S(=O)(=O)N[C@H](C(=O)O)C(C)C)cc4)cc3)c(C)c12
Reaction #57675
(S)-2-{4′-[(5-bromo-4-methoxy-3-methyl-benzofuran-2-carbonyl)-amino]-biphenyl-4-sulfonylamino}-3-methyl-butyric acid
Ausbeute 45.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)c1ccc2oc(C(=O)Nc3ccc(-c4ccc(S(=O)(=O)N[C@H](C(=O)O)C(C)C)cc4)cc3)c(C)c2c1O
Reaction #57694
(S)-2-{4′-[(5-acetyl-4-hydroxy-3-methyl-benzofuran-2-carbonyl)-amino]-biphenyl-4-sulfonylamino}-3-methyl-butyric acid
Ausbeute 47.8%DOI: 10.6084/m9.figshare.5104873.v1
COc1c(C)ccc2oc(C(=O)Nc3ccc(-c4ccc(S(=O)(=O)N[C@H](C(=O)O)C(C)C)cc4)cc3)c(C)c12
Reaction #57705
(S)-2-{4′-[(4-methoxy-3,5-dimethyl-benzofuran-2-carbonyl)-amino]-biphenyl-4-sulfonylamino}-3-methyl-butyric acid
Ausbeute 88.2%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(C(=O)Nc2ccc(-c3ccc(S(=O)(=O)N[C@H](C(=O)O)C(C)C)cc3)cc2)oc2cccc(OCCN)c12
Reaction #57769
(S)-2-(4′-{[4-(2-amino-ethoxy)-3-methyl-benzofuran-2-carbonyl]-amino}-biphenyl-4-sulfonylamino)-3-methyl-butyric acid
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1ccncc1NCc1cc2ccccc2o1
Reaction #91347
title compound
Ausbeute 3.0%DOI: 10.6084/m9.figshare.5104873.v1
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