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3044

Fc1cccc2c1CN(C1=NCCO1)C2
Reaction #1728
4-fluoro-2-(oxazolin-2-yl)isoindoline
DOI: 10.6084/m9.figshare.5104873.v1
Ic1cccc2c1CNC2
Reaction #312917
4-Iodo-2,3-dihydro-1H-isoindole
DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](Oc1ccc(S(C)(=O)=O)cc1C(=O)N1Cc2cccc(I)c2C1)C(F)(F)F
Reaction #312918
(4-Iodo-1,3-dihydro-isoindol-2-yl)-[5-methanesulfonyl-2-((S)-2,2,2-trifluoro-1-methyl ethoxy)-phenyl]-methanone
DOI: 10.6084/m9.figshare.5104873.v1
C=CC1CC1(NC(=O)C1CC(OC(=O)N2Cc3cccc(F)c3C2)CN1C(=O)OC(C)(C)C)C(=O)OCC
Reaction #371516
DOI: 10.1039/C8SC04228D
C=C[C@@H]1C[C@]1(NC(=O)[C@@H]1C[C@@H](OC(=O)N2Cc3cccc(F)c3C2)CN1C(=O)OC(C)(C)C)C(=O)OCC
Reaction #691993
4-fluoro-1,3-dihydro-isoindole-2-carboxylic acid (3R,5S)-1-tert-butoxycarbonyl-5-((1R,2S)-1-ethoxycarbonyl-2-vinyl-cyclopropylcarbamoyl)-pyrrolidin-3-yl ester
المردود 82.5%DOI: 10.6084/m9.figshare.5104873.v1
Fc1cccc2c1CCNC2
Reaction #753700
DOI: 10.1039/C8SC04228D
O=C(c1nc(-c2ccc(F)cc2)nc2ccccc12)N1CCc2c(F)cccc2C1
Reaction #804580
compound 10
المردود 27.0%DOI: 10.6084/m9.figshare.5104873.v1
Fc1cccc2c1CNC2
Reaction #923397
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CCC(n2cc(-c3cnc(N)c(N4CCc5c(F)cccc5C4)c3)cn2)CC1
Reaction #1203558
DOI: 10.1039/C8SC04228D
CCOC(=O)[C@@]12C[C@H]1/C=C\CCOCC[C@H](NC(=O)OC(C)(C)C)C(=O)N1C[C@H](OC(=O)N3Cc4cccc(F)c4C3)C[C@H]1C(=O)N2
Reaction #1259139
(2R,6S,13aS,14aR,16aS,Z)-ethyl 6-(tert-butoxycarbonylamino)-2-(4-fluoroisoindoline-2-carbonyloxy)-5,16-dioxo-2,3,5,6,7,8,10,11,13a,14,14a,15,16,16a-tetradecahydro-1H-cyclopropa(j)pyrrolo[1,2-f][1,6,9]oxadiazacyclopentadecine-14a-carboxylate
المردود 76.7%DOI: 10.6084/m9.figshare.5104873.v1
C=CCCN(CC[C@H](NC(=O)OC(C)(C)C)C(=O)N1C[C@H](OC(=O)N2Cc3cccc(F)c3C2)C[C@H]1C(=O)N[C@]1(C(=O)OCC)C[C@H]1C=C)S(=O)(=O)c1ccccc1[N+](=O)[O-]
Reaction #1259146
(3R,5S)-1-((S)-4-(N-(but-3-enyl)-2-nitrophenylsulfonamido)-2-(tert-butoxycarbonylamino)butanoyl)-5-((1R,2S)-1-(ethoxycarbonyl)-2-vinylcyclopropylcarbamoyl)pyrrolidin-3-yl 4-fluoroisoindoline-2-carboxylate
المردود 84.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(Oc1ccc(S(C)(=O)=O)cc1C(=O)N1Cc2cccc(I)c2C1)C(F)(F)F
Reaction #1302313
DOI: 10.1039/C8SC04228D
CC[C@@H]1CC(C)CC/C=C\[C@@H]2C[C@@]2(C(=O)NS(=O)(=O)C2(C)CC2)NC(=O)[C@@H]2C[C@@H](OC(=O)N3Cc4cccc(F)c4C3)CN2C(=O)[C@H]1NC(=O)OC(C)(C)C
Reaction #1568839
(2R,6S,7R,13aS,14aR,16aS,Z)-6-((tert-butoxycarbonyl)amino)-7-ethyl-9-methyl-14a-(((1-methylcyclopropyl)sulfonyl)carbamoyl)-5,16-dioxo-1,2,3,5,6,7,8,9,10,11,13a,14,14a,15,16,16a-hexadecahydrocyclopropa[e]pyrrolo[1,2-a][1,4]diazacyclopentadecin-2-yl 4-fluoroisoindoline-2-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1cn(C2CC2)c2cc(N3Cc4cccc(F)c4C3)c(F)cc2c1=O
Reaction #1581924
target compound
المردود 43.4%DOI: 10.6084/m9.figshare.5104873.v1
CC1COc2c(N3Cc4cccc(F)c4C3)c(F)cc3c(=O)c(C(=O)O)cn1c23
Reaction #1581925
target compound
المردود 35.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1cn(C2CC2)c2c(F)c(N3Cc4cccc(F)c4C3)c(F)cc2c1=O
Reaction #1581926
target compound
المردود 66.1%DOI: 10.6084/m9.figshare.5104873.v1
Nc1c(F)c(N2Cc3cccc(F)c3C2)c(F)c2c1c(=O)c(C(=O)O)cn2C1CC1
Reaction #1581941
target compound
المردود 21.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1cn(-c2ccc(F)cc2)c2c(F)c(N3Cc4cccc(F)c4C3)c(F)cc2c1=O
Reaction #1581963
target compound
المردود 82.9%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1cn(-c2ccc(F)cc2F)c2c(F)c(N3Cc4cccc(F)c4C3)c(F)cc2c1=O
Reaction #1581964
target compound
المردود 81.9%DOI: 10.6084/m9.figshare.5104873.v1
Fc1cccc2c1CNC2
Reaction #1582017
4-fluoroisoindoline
المردود 55.8%DOI: 10.6084/m9.figshare.5104873.v1
الصفحة 1التالي