Recherche de Sous-structure

13282

COc1ccc(CN2CC(c3cccc(F)c3F)=CC[C@@H](NC(=O)OCc3ccccc3)C2=O)c(OC)c1
Reaction #42664
title compound
Rendement 57.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@@H]1CC=C(c2cccc(F)c2F)CNC1=O)OCc1ccccc1
Reaction #42665
title compound
Rendement 66.4%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CN2CC(c3cccc(F)c3F)=CC[C@@H](NC(=O)OCc3ccccc3)C2=O)c(OC)c1
Reaction #48408
title compound
Rendement 57.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@@H]1CC=C(c2cccc(F)c2F)CNC1=O)OCc1ccccc1
Reaction #48409
title compound
Rendement 66.4%DOI: 10.6084/m9.figshare.5104873.v1
Cl.Cl.NCC1NCCc2cc(O)c(O)cc21
Reaction #55440
1-aminomethyl-6,7-dihydroxy-1,2,3,4-tetrahydroisoquinoline dihydrochloride
Rendement 61.8%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(N2CCN(C(=O)C[C@@H](OC(=O)NCCc3ccccc3)c3ccccc3)CC2)cc1OC
Reaction #72490
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCC(NC(=O)OCc1ccccc1)C1(c2ccc(OC)cc2)CCC(=O)CC1
Reaction #73473
ketone
DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H](C)[C@H](NC(=O)[C@@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](Cc1ccccc1)NC(=O)OCc1ccccc1)C(C)C)C(=O)N[C@@H](Cc1c[nH]cn1)C(N)=O
Reaction #93624
title compound
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #93651
B7
DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H](C)[C@H](NC(=O)[C@@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](Cc1ccccc1)NC(=O)OCc1ccccc1)C(C)C)C(=O)N[C@@H](Cc1c[nH]cn1)C(N)=O
Reaction #93655
title compound
DOI: 10.6084/m9.figshare.5104873.v1
N=C(N)NCCCCNC(=O)[C@@H]1CCCN1C(=O)[C@@H](Cc1ccccc1)NC(=O)OCc1ccccc1.OCl
Reaction #95985
Benzyloxycarbonyl-D-phenylalanyl-L-prolyl-agmatine-chlorohydrate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)N1c2cc3c(cc2C(NC(=O)OCc2ccccc2)CC1C)CCC3
Reaction #188348
DOI: 10.1039/C8SC04228D
CC(C)C(CCNC(=N)N)CC(O)C(CC1CCCCC1)NC(=O)C(Cc1c[nH]cn1)NC(=O)C(Cc1ccccc1)NC(=O)OC(C)(C)C
Reaction #188495
DOI: 10.1039/C8SC04228D
NC1CN(C(=O)NS(=O)(=O)Nc2ccncc2)C1=O
Reaction #190468
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1C2CSCC(Cc3ccc(NC(=O)OCc4ccccc4)c(F)c3)C2OC1(C)C
Reaction #191314
DOI: 10.1039/C8SC04228D
CC(C)(C)N1C(=O)CC(c2ccc(CC(NC(=O)OCc3ccccc3)C(N)=O)cc2)S1(=O)=O
Reaction #200412
DOI: 10.1039/C8SC04228D
O=C(Nc1cc(C(=O)O)ccc1F)OCc1ccccc1
Reaction #204816
DOI: 10.1039/C8SC04228D
O=C(COc1ccc(CCCCNC(=O)OCc2ccccc2)cc1)Nc1ccccc1
Reaction #219738
amide
Rendement 99.1%DOI: 10.6084/m9.figshare.5104873.v1
NCCCCc1ccc(OCC(=O)Nc2ccccc2)cc1
Reaction #219739
amine
Rendement 97.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ccc(O)c(C(=O)O)c1)OCc1ccccc1
Reaction #239438
DOI: 10.1039/C8SC04228D
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