Substructure Search

CCOC(=O)CCCCCCCCCCN

CCOC(CCNC(=O)CCCCCCCCCCNC(=O)OCC1c2ccccc2-c2ccccc21)OCC
Reaction #53978
9H-fluoren-9-ylmethyl 11-[(3,3-diethoxypropyl)amino]-11-oxoundecyl-carbamate
Yield 23.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)CCCCCCCCCC[N+](=O)[O-]
Reaction #72398
solid
Yield 42.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CCC2C3CCC4CC(OC(C)=O)C(OCC)CC4(C)C3C(NC(=O)OCC(Cl)(Cl)Cl)CC12C
Reaction #181349
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)CCCCCCCCCC[N+](=O)[O-]
Reaction #187170
DOI: 10.1039/C8SC04228D
COC(=O)C1CCC2C3CCC4CC(O)C(O)CC4(C)C3C(NCCC(C)C)CC12C
Reaction #298704
DOI: 10.1039/C8SC04228D
O=C(O)CCCCCCCCCCn1c(-c2ccccc2)nc(-c2ccccc2)c1-c1ccccc1
Reaction #352546
1-(10-carboxydecyl)-2,4,5-triphenylimidazole
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)[C@@H](CCCCCCC1CCN(C(=O)OCc2ccccc2)CC1)N[C@H]1COc2ccccc2N(CC(=O)OC(C)(C)C)C1=O
Reaction #368149
tert-butyl 3(S)-[7-(1-benzyloxycarbonyl-4-piperidyl)-1(R)-ethoxycarbonylheptyl]amino-4-oxo-2,3,4,5-tetrahydro-1,5-benzoxazepine-5-acetate
Yield 7.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CN1C(=O)[C@@H](N[C@H](CCCCCCC2CCNCC2)C(=O)O)COc2ccccc21
Reaction #368150
3(S)-[1(R)-carboxy-7-(4-piperidyl)heptyl]amino-4-oxo-2,3,4,5-tetrahydro-1,5-benzoxazepine-5-acetic acid
Yield 42.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CN1C(=O)[C@@H](N[C@@H](CCCCCCC2CCNCC2)C(=O)O)COc2ccccc21
Reaction #368151
3(S)-[1(S)-carboxy-7-(4-piperidyl)heptyl]amino-4-oxo-2,3,4,5-tetrahydro-1,5-benzoxazepine-5-acetic acid
Yield 63.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CCCCCCCCCCn1c(-c2ccccc2)nc(-c2ccccc2)c1-c1ccccc1
Reaction #369688
DOI: 10.1039/C8SC04228D
CCOC(=O)C1CCC2C3CCC4CC(OC(C)=O)C(OCC)CC4(C)C3C(NCCC(C)C)CC12C
Reaction #395576
DOI: 10.1039/C8SC04228D
CCOC(=O)CCCCCCCCCCNC(=O)CN(CCN(CCN(CC(=O)O)CC(=O)O)CC(=O)O)CC(=O)O
Reaction #430036
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H]1OC(=O)[C@H](C)C(=O)[C@H](C)[C@@H](OC2O[C@H](C)C[C@H](N(C)C)[C@H]2O)[C@@](C)(OC)C[C@@H](C)C(=O)[C@H](C)[C@H]2N(CCN(C)Cc3ccnc4ccccc34)C(=O)O[C@]12CC
Reaction #440944
(3aS,4R,7R,9R,10R,11S,13R,15R,15aR)-3a,4-diethyl-11-methoxy-7,9,11,13,15-pentamethyl-1-{2-[methyl-(quinolin-4-ylmethyl)amino]ethyl}-2,6,8,14-tetraoxotetradecahydro-2H-oxacyclotetradecino[4,3-d][1,3]oxazol-10-yl 3,4,6-trideoxy-3-(dimethylamino)-D-xylo-hexopyranoside
Yield 18.0%DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H]1OC(=O)[C@H](C)C(=O)[C@H](C)[C@@H](OC2O[C@H](C)C[C@H](N(C)C)[C@H]2O)[C@@](C)(OC)C[C@@H](C)C(=O)[C@H](C)[C@H]2N(CCN(C)Cc3cncc(-c4cccnc4)c3)C(=O)O[C@]12CC
Reaction #440945
(3aS,4R,7R,9R,10R,11S,13R,15R,15aR)-1-{2-[(3,3′-bipyridin-5-ylmethyl)(methyl)amino]ethyl }-3a,4-diethyl-11-methoxy-7,9,11,13,15-pentamethyl-2,6,8,14-tetraoxotetradecahydro-2H-oxacyclotetradecino[4,3-d][1,3]oxazol-10-yl 3,4,6-trideoxy-3-(dimethylamino)-D-xylo-hexopyranoside
Yield 27.0%DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H]1OC(=O)[C@H](C)C(=O)[C@H](C)[C@@H](OC2O[C@H](C)C[C@H](N(C)C)[C@H]2O)[C@](C)(OC)C[C@@H](C)C(=O)[C@H](C)[C@H]2N(CCCCn3cnc(-c4cccnc4)c3)C(=O)O[C@]12CO
Reaction #440946
(3aR,4R,7R,9R,10R,11R,13R,15R,15aR)-4-ethyl-3a-(hydroxymethyl)-11-methoxy-7,9,11,13,15-pentamethyl-2,6,8,14-tetraoxo-1-[4-(4-pyridin-3-yl-1H-imidazol-1-yl)-butyl]tetradecahydro-2H-oxacyclotetradecino[4,3-d][1,3]oxazol-10-yl 3,4,6-trideoxy-3-(dimethylamino)-D-xylo-hexopyranoside
Yield 48.0%DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H]1OC(=O)[C@H](C)C(=O)[C@H](C)[C@@H](OC2O[C@H](C)C[C@H](N(C)C)[C@H]2O)[C@](C)(OC)C[C@@H](C)C(=O)[C@H](C)[C@H]2N(CCCCn3cnc(-c4cccnc4)c3)C(=O)O[C@]12C=O
Reaction #440947
(3aS,4R,7R,9R,10R,11R,13R,15R,15aR)-4-ethyl-3a-formyl-11-methoxy-7,9,11,13,15-pentamethyl-2,6,8,14-tetraoxo-1-[4-(4-pyridin-3-yl-1H-imidazol-1-yl)butyl]tetradecahydro-2H-oxacyclotetradecino[4,3-d][1,3]oxazol-10-yl 3,4,6-trideoxy-3-(dimethylamino)-D-xylo-hexopyranoside
Yield 19.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCCCCCCCCCNC(=O)CN(CCN(CCN(CC(=O)O)CC(=O)O)CC(=O)O)CC(=O)O
Reaction #500172
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)CCCCCCCCCC[N+](=O)[O-]
Reaction #511473
solid
Yield 42.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)[C@H]1CC[C@H]2[C@@H]3CC[C@H]4C[C@H](OC(C)=O)[C@@H](OCC)C[C@]4(C)[C@H]3[C@H](NC(=O)OCC(Cl)(Cl)Cl)C[C@]12C
Reaction #549619
foam
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)[C@H]1CC[C@H]2[C@@H]3CC[C@H]4C[C@H](OC(C)=O)[C@@H](OCC)C[C@]4(C)[C@H]3[C@H](NCCC(C)C)C[C@]12C
Reaction #549621
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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