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1329621

O=C(/C=C/CCl)N1CCc2c(sc3ncnc(Nc4ccc(Cl)c(Cl)c4)c23)C1
Reaction #66824
solid
المردود 58.9%DOI: 10.6084/m9.figshare.5104873.v1
O=C(/C=C/CN1CCNCC1)N1CCc2c(sc3ncnc(Nc4ccc(F)c(Cl)c4)c23)C1
Reaction #66849
title compound
المردود 87.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(/C=C/CN1CCC1)N1CCc2c(sc3ncnc(Nc4ccc(Cl)c(Cl)c4)c23)C1
Reaction #66852
title compound
المردود 13.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C(/C=C/CN1CCCOCC1)N1CCc2c(sc3ncnc(Nc4ccc(Cl)c(Cl)c4)c23)C1
Reaction #66853
title compound
المردود 80.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(/C=C/CN1CCN(c2ccccn2)CC1)N1CCc2c(sc3ncnc(Nc4ccc(Cl)c(Cl)c4)c23)C1
Reaction #66854
title compound
المردود 79.7%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCC2CN(C/C=C/C(=O)N3CCc4c(sc5ncnc(Nc6ccc(Cl)c(Cl)c6)c45)C3)CC21
Reaction #66855
N-(3,4-Dichlorophenyl)-7-[(2E)-4-(1-methylhexahydropyrrolo[3,4-b]pyrrol-5(1H)-yl)but-2-enoyl]-5,6,7,8-tetrahydropyrido[4′,3′:4,5]thieno[2,3-d]pyrimidin-4-amine
DOI: 10.6084/m9.figshare.5104873.v1
O=C(/C=C/CN1CCN(C(=O)N2CCCC2)CC1)N1CCc2c(sc3ncnc(Nc4ccc(Cl)c(Cl)c4)c23)C1
Reaction #66879
title compound
المردود 10.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C/C=C/C(=O)N1CCc2c(sc3ncnc(Nc4cc(O)cc(Cl)c4)c23)C1
Reaction #66880
3-Chloro-5-({7-[(2E)-4-(dimethylamino)but-2-enoyl]-5,6,7,8-tetrahydropyrido[4′,3′:4,5]thieno[2,3-d]pyrimidin-4-yl}amino)phenol
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)N(C)C/C=C/C(=O)N1CCc2c(sc3ncnc(Nc4cc(O)cc(Cl)c4)c23)C1
Reaction #66881
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COCCN(C)C/C=C/C(=O)N1CCc2c(sc3ncnc(Nc4cc(O)cc(Cl)c4)c23)C1
Reaction #66882
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COCCN(C/C=C/C(=O)N1CCc2c(sc3ncnc(Nc4cc(O)cc(Cl)c4)c23)C1)CCOC
Reaction #66883
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC1CCN(C/C=C/C(=O)N2CCc3c(sc4ncnc(Nc5cc(O)cc(Cl)c5)c34)C2)CC1
Reaction #66884
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C(=O)N1CCN(C/C=C/C(=O)N2CCc3c(sc4ncnc(Nc5cc(O)cc(Cl)c5)c34)C2)CC1
Reaction #66885
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(/C=C/CN1CCCOCC1)N1CCc2c(sc3ncnc(Nc4cc(O)cc(Cl)c4)c23)C1
Reaction #66886
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(/C=C/CN1CC2CCC(C1)O2)N1CCc2c(sc3ncnc(Nc4cc(O)cc(Cl)c4)c23)C1
Reaction #66887
title compound
المردود 38.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C(/C=C/CN1CC2CCC(C2)C1)N1CCc2c(sc3ncnc(Nc4cc(O)cc(Cl)c4)c23)C1
Reaction #66888
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(/C=C/CN1CC2CCC(C2)C1)N1CCc2c(sc3ncnc(Nc4cc(O)c(Cl)c(Cl)c4)c23)C1
Reaction #66891
5-({7-[(2E)-4-(3-Azabicyclo[3.2.1]oct-3-yl)but-2-enoyl]-5,6,7,8-tetrahydropyrido[4′,3′:4,5]thieno[2,3-d]pyrimidin-4-yl}amino)-2,3-dichlorophenol
DOI: 10.6084/m9.figshare.5104873.v1
CN(C)CC=CC(=O)N1CCc2c(sc3ncnc(Nc4cc(O)cc(Cl)c4)c23)C1
Reaction #899784
DOI: 10.1039/C8SC04228D
CC(C)N(C)CC=CC(=O)N1CCc2c(sc3ncnc(Nc4cc(O)cc(Cl)c4)c23)C1
Reaction #1290264
DOI: 10.1039/C8SC04228D
O=C(C=CCN1CCNCC1)N1CCc2c(sc3ncnc(Nc4ccc(F)c(Cl)c4)c23)C1
Reaction #2402982
DOI: 10.1039/C8SC04228D