Substructure Search

CCCCCCCCCCCCCCCCCCO

CCCCCCCCC1CCC2C3CC=C4CC(OC(=O)NCCCCCC(=O)N5CC(OC(=O)CCC(=O)O)CC5C(OC(c5ccc(OC)cc5)c5ccc(OC)cc5)c5ccccc5)CCC4(C)C3CCC12C
Reaction #49173
compound 8
Yield 89.5%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C(OC(c2ccccc2)C2CN(C(=O)CCCCCNC(=O)OC3CCC4(C)C(=CCC5C4CCC4(C)C(C(C)CCCC(C)C)CCC54)C3)CC2O)c2ccc(OC)cc2)cc1
Reaction #49193
Compound 66
Yield 90.5%DOI: 10.6084/m9.figshare.5104873.v1
C1CCNC1.CC(C)CCC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3CC=C4C[C@@H](OP(N)O)CC[C@]4(C)[C@H]3CC[C@]12C
Reaction #49194
67
Yield 84.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C(OC(c2ccccc2)C2CN(C(=O)CCCCCNC(=O)OC3CCC4(C)C(=CCC5C4CCC4(C)C(C(C)CCCC(C)C)CCC54)C3)CC2OC(=O)CCC(=O)O)c2ccc(OC)cc2)cc1
Reaction #49195
compound 68
Yield 91.2%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCCCCN(CCCCCCCCCCCCCCCCCC)C(=O)CCC(C)C1CCC2C3CCC4CC(OC(=O)NCCCCCC(=O)N5CC(OC(=O)CCC(=O)O)CC5C(OC(c5ccc(OC)cc5)c5ccc(OC)cc5)c5ccccc5)CCC4(C)C3CCC12C
Reaction #49206
compound 86
Yield 71.5%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCCCCNC(=O)CCC(C)C1CCC2C3CCC4CC(OC(=O)NCCCCCC(=O)N5CC(O)CC5C(OC(c5ccc(OC)cc5)c5ccc(OC)cc5)c5ccccc5)CCC4(C)C3CCC12C
Reaction #49209
Compound 90
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCCCC(=O)OCCOc1ccc(C2C(=O)Oc3c2cc(C(C)(C)C)cc3C(C)(C)C)cc1
Reaction #50778
5,7-di-tert-butyl-3-[4-(2-stearoyloxyethoxy)phenyl]benzofuran-2-one
Yield 89.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CCC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3CC=C4C[C@@H](O)CC[C@]4(C)[C@H]3CC[C@]12C.CCNC(=N)CCCSSc1ccccn1
Reaction #53250
Cholesterol ethylamidinopropyl-pyridyldisulfide
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCCCCC[C@H]1C2OCCOC2C[C@@H]1CCC(=O)CCC=C(C)C
Reaction #55563
9-ethylenedioxy-15-keto-19-methyl-prost-18-enoic acid, methyl ester
Yield 88.2%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCCCCC[C@H]1C2OCCOC2C[C@@H]1CCC(=O)CCC=C(C)C
Reaction #55564
9-ethylenedioxy-15-keto-19-methyl-prost-18-enoic acid, methyl ester
Yield 94.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ccccc1O)c1ccc(F)cc1
Reaction #87914
4-Fluoro-N-(2-hydroxyphenyl)-benzamide
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OC[C@H]1O[C@H](O[C@@H]2[C@H](OC(C)=O)[C@@H](O[C@@H]3[C@@H](OCCCn4cc(CO[C@H]5CC[C@@]6(C)C(CC[C@H]7[C@@H]8CC[C@H]([C@H](C)CCCC(C)C)[C@@]8(C)CC[C@@H]76)C5)nn4)O[C@H](COC(C)=O)[C@@H](OC(C)=O)[C@@H]3OC(C)=O)O[C@H](COC(C)=O)[C@H]2OC(C)=O)[C@@H](OC(C)=O)[C@@H](OC(C)=O)[C@@H]1OC(C)=O
Reaction #162019
triazole
Yield 81.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CCC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3CCC4C[C@@H](OCc5cn(CCCO[C@H]6O[C@H](COC(=O)c7ccccc7)[C@@H](OC(=O)c7ccccc7)[C@H](O[C@H]7O[C@H](COC(=O)c8ccccc8)[C@@H](OC(=O)c8ccccc8)[C@H](O[C@H]8O[C@H](COC(=O)c9ccccc9)[C@@H](OC(=O)c9ccccc9)[C@H](OC(=O)c9ccccc9)[C@@H]8OC(=O)c8ccccc8)[C@@H]7OC(=O)c7ccccc7)[C@@H]6OC(=O)c6ccccc6)nn5)CC[C@]4(C)[C@H]3CC[C@]12C
Reaction #162024
triazole
Yield 72.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CCC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3CCC4C[C@@H](OCc5cn(CCCO[C@H]6O[C@H](CO)[C@@H](O)[C@H](O[C@H]7O[C@H](CO)[C@@H](O)[C@H](O[C@H]8O[C@H](CO)[C@@H](O)[C@H](O)[C@@H]8O)[C@@H]7O)[C@@H]6O)nn5)CC[C@]4(C)[C@H]3CC[C@]12C
Reaction #162025
polyol
DOI: 10.6084/m9.figshare.5104873.v1
CC1CCC2(OC1)OC1CC3C4CCC5CC(=O)C6OC6C5(C)C4CCC3(C)C1C2C
Reaction #174290
DOI: 10.1039/C8SC04228D
CCCCCCC(CCCCCCCCCCC(=O)O)O[Si](C)(C)C(C)(C)C
Reaction #186793
DOI: 10.1039/C8SC04228D
CCCCCCCCCCCCCCCCCCOC1CC(COc2ccc3c(c2)C(O)(c2ccc(Cl)cc2)c2ccccc2-3)CC(OCCCCCCCCCCCCCCCCCC)C1OCCCCCCCCCCCCCCCCCC
Reaction #195382
DOI: 10.1039/C8SC04228D
CC1CCC2(OC1)OC1CC3C4CCC5CC(=O)C=CC5(C)C4CCC3(C)C1C2C
Reaction #200852
DOI: 10.1039/C8SC04228D
CCCCCCCCCCCCCCCCCCOc1cc(OCCCOc2cccc([N+](=O)[O-])c2)cc(C(=O)N(CC(=O)OCC)CC(=O)OCC)c1
Reaction #202483
DOI: 10.1039/C8SC04228D
CCCCCCCCCCCCCCCCCCOC(=O)N1CCCCC1CCOS(=O)(=O)c1ccc(C)cc1
Reaction #205814
DOI: 10.1039/C8SC04228D
Page 1Next