Recherche de Sous-structure

CCN(CCO)c1ccccc1

CC(C)CN1C(=O)[C@@H](CC(=O)OCOC(=O)C(C)(C)C)O[C@H](c2ccccc2Cl)c2cc(Cl)ccc21
Reaction #1867
trans-7-chloro-5-(2-chlorophenyl)-1-isobutyl-2-oxo-1,2,3,5-tetrahydro-4,1-benzoxazepine-3-acetic acid pivaloyloxymethyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CCCCN1CCOc2c(-c3ncco3)cc(C(=O)N[C@@H](Cc3cc(F)cc(F)c3)[C@H](O)CNCc3cccc(CC)c3)cc21
Reaction #42468
title compound
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
Rendement 96.0%DOI: 10.6084/m9.figshare.5104873.v1
CSc1ccc(N2CCOCC2)c(C(=O)O)c1
Reaction #61000
title compound
Rendement 10.1%DOI: 10.6084/m9.figshare.5104873.v1
CSc1ccc(N2CCOCC2)c(C(=O)N2CCN(c3ccc(C(C)=O)cc3F)CC2)c1
Reaction #61001
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCO[C@@H]1CN(c2ccc3c(=O)c(C(=O)O)cn(C4CC4)c3c2OC)CC[C@@H]1NC(=O)c1nc(Cl)c(CC)[nH]1
Reaction #72011
title compound
Rendement 62.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1c2ccccc2C(C)(C)C12C=Cc1c(cc(N3CCOCC3)c3ccccc13)O2
Reaction #82880
indoline-2,3'-[3H]-naphtho[2,1-b]pyran
Rendement 34.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC[C@@H](CNc2nc(-c3ccc(N4CCOCC4)cc3)cc3nccnc23)C1
Reaction #85880
title compound
Rendement 73.0%DOI: 10.6084/m9.figshare.5104873.v1
c1cnc2c(N3CC4CCNC4C3)nc(-c3ccc(N4CCOCC4)cc3)cc2n1
Reaction #85886
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CC(CNc2nc(-c3ccc(N4CCOCC4)cc3)cc3nccnc23)CC(F)(F)C1
Reaction #85892
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CC(O)CC(CNc2nc(-c3ccc(N4CCOCC4)cc3)cc3nccnc23)C1
Reaction #85894
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](O)C1CCN(c2nc(-c3ccc(N4CCOCC4)cc3)cc3nccnc23)C1
Reaction #85902
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(OC)C1(C)Oc2ccc([N+](=O)[O-])cc2C(N(Cc2nnn(C)n2)c2ccccc2C(C)C)C1O
Reaction #192396
DOI: 10.1039/C8SC04228D
CC1(C)OCCn2c1nc(C(=O)NCc1ccc(F)cc1N1C(=O)CCC1CN=[N+]=[N-])c(OCc1ccccc1)c2=O
Reaction #193348
DOI: 10.1039/C8SC04228D
CCOC(=O)C(CCCCCCCN1C(=O)c2ccccc2C1=O)NC1CSc2ccccc2N(CC(=O)O)C1=O
Reaction #200914
DOI: 10.1039/C8SC04228D
O=C(Nc1cc(Nc2ccc(N3CCOCC3)cc2)ncn1)Nc1c(Cl)cccc1Cl
Reaction #205445
DOI: 10.1039/C8SC04228D
CC1(C)OCCn2c1nc(C(=O)NCc1ccc(F)cc1N1C(=O)CCC1CO)c(OCc1ccccc1)c2=O
Reaction #207883
DOI: 10.1039/C8SC04228D
CCOC(=O)N(C)CC1CN(c2c(F)cc(C(=O)O)c(F)c2F)CCO1
Reaction #208796
DOI: 10.1039/C8SC04228D
CN1CCN(c2cccc3c2C[C@H](NC(=O)c2ccc(N4CCOCC4)cc2)CO3)CC1
Reaction #218309
title compound
Rendement 68.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1cc(Nc2ccc(N3CCOCC3)cc2)ncn1)Nc1c(F)cccc1F
Reaction #222297
DOI: 10.1039/C8SC04228D
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