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1204414

CN(Cc1cc2ccccc2o1)C(=O)/C=C/c1cnc2c(c1)CCC(=O)N2
Reaction #46619
title compound
المردود 90.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(C(=O)c2c(N3CCN(C(=O)c4ccco4)CC3)n(-c3ccccc3)c3ccccc23)CC1
Reaction #54487
2-[4-(2-furoyl)-1-piperazinyl]-1-phenyl-indole 3-carboxylic acid 4-methyl-piperazide
DOI: 10.6084/m9.figshare.5104873.v1
C=Cc1cccc2oc(C(=O)Nc3ccc(-c4ccc(S(=O)(=O)N(C)[C@H](C(=O)OC)C(C)C)cc4)cc3)c(C)c12
Reaction #57612
methyl N-methyl-N-[(4′-{[(3-methyl-4-vinyl-1-benzofuran-2-yl)carbonyl]amino}-1,1′-biphenyl-4-yl)sulfonyl]-L-valinate
المردود 63.4%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H](NS(=O)(=O)c1ccc(-c2ccc(NC(=O)c3oc4cccc(OC(C)C)c4c3C)cc2)cc1)C(C)C
Reaction #57632
(S)-2-{4′-[(4-Isopropoxy-3-methyl-benzofuran-2-carbonyl)-amino]-biphenyl-4-sulfonylamino}-3-methyl-butyric acid methyl ester
المردود 75.2%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(OC(C)C)c12
Reaction #57633
(S)-2-{4′-[(4-isopropoxy-3-methyl-benzofuran-2-carbonyl)-amino]-biphenyl-4-sulfonylamino}-3-methyl-butyric acid
المردود 79.2%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H](NS(=O)(=O)c1ccc(-c2ccc(NC(=O)c3oc4cccc(-c5cccc([N+](=O)[O-])c5)c4c3C)cc2)cc1)C(C)C
Reaction #57640
(S)-3-methyl-2-(4′-{[3-methyl-4-(3-nitro-phenyl)-benzofuran-2-carbonyl]-amino}-biphenyl-4-sulfonylamino)-butyric acid methyl ester
المردود 18.8%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(-c3cccc([N+](=O)[O-])c3)c12
Reaction #57641
(S)-3-methyl-2-(4′-{[3-methyl-4-(3-nitro-phenyl)-benzofuran-2-carbonyl]-amino}-biphenyl-4-sulfonylamino)-butyric acid
المردود 72.3%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H](NS(=O)(=O)c1ccc(-c2ccc(NC(=O)c3oc4ccc(Cl)c(OC)c4c3C)cc2)cc1)C(C)C
Reaction #57664
(S)-2-{4′-[(5-chloro-4-methoxy-3-methyl-benzofuran-2-carbonyl)-amino]-biphenyl-4-sulfonylamino}-3-methyl-butyric acid methyl ester
المردود 87.0%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
المردود 62.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H](NS(=O)(=O)c1ccc(-c2ccc(NC(=O)c3oc4ccc(Br)c(OC)c4c3C)cc2)cc1)C(C)C
Reaction #57674
(S)-2-{4′-[(5-bromo-4-methoxy-3-methyl-benzofuran-2-carbonyl)-amino]-biphenyl-4-sulfonylamino}-3-methyl-butyric acid methyl ester
المردود 23.0%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
المردود 45.5%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 #57679
(R)-2-{4′-[(5-bromo-4-methoxy-3-methyl-benzofuran-2-carbonyl)-amino]-biphenyl-4-sulfonylamino}-3-methyl-butyric acid
المردود 56.3%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H](NS(=O)(=O)c1ccc(-c2ccc(NC(=O)c3oc4ccc(I)c(OC)c4c3C)cc2)cc1)C(C)C
Reaction #57683
(S)-2-{4′-[(5-iodo-4-methoxy-3-methyl-benzofuran-2-carbonyl)-amino]-biphenyl-4-sulfonylamino}-3-methyl-butyric acid methyl ester
المردود 47.5%DOI: 10.6084/m9.figshare.5104873.v1
C=C(Cl)c1ccc2oc(C(=O)Nc3ccc(-c4ccc(S(=O)(=O)N[C@H](C(=O)OC)C(C)C)cc4)cc3)c(C)c2c1OC
Reaction #57690
(S)-2-(4′-{[5-(1-chloro-vinyl)-4-methoxy-3-methyl-benzofuran-2-carbonyl]-amino}-biphenyl-4-sulfonylamino)-3-methyl-butyric acid methyl ester
المردود 20.0%DOI: 10.6084/m9.figshare.5104873.v1
C=C(Cl)c1ccc2oc(C(=O)Nc3ccc(-c4ccc(S(=O)(=O)N[C@H](C(=O)O)C(C)C)cc4)cc3)c(C)c2c1OC
Reaction #57691
(S)-2-(4′-{[5-(1-chloro-vinyl)-4-methoxy-3-methyl-benzofuran-2-carbonyl]-amino}-biphenyl-4-sulfonylamino)-3-methyl-butyric acid
المردود 81.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccc(Nc2nccc(-c3ccc(S(=O)(=O)N4CCOCC4)cc3)n2)cc1)N1CCN(C(=O)c2ccco2)CC1
Reaction #61740
[4-(furan-2-carbonyl)piperazin-1-yl](4-{4-[4-(morpholine-4-sulfonyl)-phenyl]pyrimidin-2-ylamino}phenyl)methanone
المردود 52.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)N(C)C/C=C/C(=O)N1CCc2c(oc3ncnc(Nc4ccc(F)c(Cl)c4)c23)C1
Reaction #66868
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C/C=C/C(=O)N1CCc2c(oc3ncnc(Nc4ccc(OCc5cccc(F)c5)c(Cl)c4)c23)C1
Reaction #66902
title compound
المردود 38.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)c1ccc(Cn2ncc([N+](=O)[O-])n2)o1
Reaction #71020
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1(c2ccc(Cn3ncc([N+](=O)[O-])n3)o2)OCCO1
Reaction #71021
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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