子结构搜索

C1CCC(CC1)O

OC1(C(CN2CCNCC2)c2cccc(Cl)c2)CCCCC1
Reaction #57081
1-[1-(3-chlorophenyl)-2-piperazin-1-ylethyl]cyclohexanol
收率 99.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(CC(c2ccc(OCc3ccc(C(F)(F)F)cc3)c(F)c2)C2(O)CCCCC2)CC1.Cl.Cl
Reaction #57124
1-[1-(3-fluoro-4-{[4-(trifluoromethyl)benzyl]oxy}phenyl)-2-(4-methylpiperazin-1-yl)ethyl]cyclohexanol Dihydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
Cc1[nH]c(/C=C2\C(=O)Nc3ccc(F)cc32)c(C)c1C(=O)N[C@H]1CCCC[C@@H]1O
Reaction #66310
title compound
收率 74.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C1(C)SC(N[C@H]2CCCC[C@@H]2O)=NC1=O
Reaction #74427
2-((1S,2S)-2-hydroxycyclohexylamino)-5-isopropyl-5-methylthiazol-4(5H)-one
DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C1(CNC(=O)c2ccc(C(F)(F)F)cc2)CCC2(CC1)OCCO2
Reaction #95966
α,α,α-trifluoro-N-[[8-(dimethylamino)-1,4-dioxaspiro[4.5]dec-8-yl]methyl]-p-toluamide
DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCc1ccncc1)OC1CCC(CNC(=O)N2CCCC2)CC1
Reaction #155672
compound
收率 25.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)C1CCC(Oc2ccc(C(=O)O)cn2)CC1
Reaction #176271
DOI: 10.1039/C8SC04228D
NC1CCC(Oc2ccc3c(=O)[nH]ccc3c2)CC1
Reaction #198494
DOI: 10.1039/C8SC04228D
COc1ccc2c(c1)C13CCN(C)C(C2)C1CC1(CC3)OCCO1
Reaction #201951
DOI: 10.1039/C8SC04228D
COc1ccc(C2(O)CCC(N3CC(NC(=O)CNC(=O)c4cccc(C)c4)C3)CC2)cn1
Reaction #207039
DOI: 10.1039/C8SC04228D
COc1ccc(C2(O)CCC(N3CC(NC(=O)CNC(=O)c4cc(F)c(F)c(F)c4)C3)CC2)cn1
Reaction #207598
DOI: 10.1039/C8SC04228D
C=CCC1CCC2(CC1c1ccc(C(C)(C)CCCCCC)cc1OCc1ccccc1)OCCO2
Reaction #212683
DOI: 10.1039/C8SC04228D
COc1ccc2nccc(CCC3(O)CCC(N)CC3)c2n1
Reaction #223206
DOI: 10.1039/C8SC04228D
O=C(NC1CCCCC1OCCO)c1cn(-c2ccc(Cl)cc2)c(-c2ccccc2Cl)n1
Reaction #224526
DOI: 10.1039/C8SC04228D
O=C(NC1CCCCC1O)c1nc(-c2ccc(Cl)cc2)c(OCC2CC2)nc1C(F)(F)F
Reaction #226572
DOI: 10.1039/C8SC04228D
O=C(NC1CCC(CCN2CCC(c3cccc4c3OCO4)CC2)CC1)C1(O)CCCCC1
Reaction #229331
DOI: 10.1039/C8SC04228D
CCOC(=O)C1C(CNCc2ccccc2)CCC(OC(C)c2cc(C(F)(F)F)cc(C(F)(F)F)c2)C1c1ccc(F)cc1
Reaction #238063
DOI: 10.1039/C8SC04228D
CC1CCC(C(C)C)C(OC(=O)CC(NC(=O)OCc2ccccc2)(C(N)=O)C(=O)OC(C)(C)C)C1
Reaction #240738
DOI: 10.1039/C8SC04228D
CC(C)(C)[Si](C)(C)OC1CCC(Nc2cnnn2Cc2ccccc2)CC1
Reaction #249911
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)NC1CCC(Oc2cccc3c(N)nccc23)CC1
Reaction #256404
DOI: 10.1039/C8SC04228D
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