部分構造検索

248505

OC1(C(CN2CCNCC2)c2cccc(Cl)c2)CCCCC1

Reaction #57081

1-[1-(3-chlorophenyl)-2-piperazin-1-ylethyl]cyclohexanol

収率 99.0%DOI: 10.6084/m9.figshare.5104873.v1

CC(C)(C)OC(=O)NC1CCN(CC(c2ccc(Cl)c(Cl)c2)C2(O)CCCCC2)CC1

Reaction #57084

tert-butyl {1-[2-(3,4-dichlorophenyl)-2-(1-hydroxycyclohexyl)ethyl]piperidin-4-yl}carbamate

収率 53.0%DOI: 10.6084/m9.figshare.5104873.v1

CC(c1cccc(OC(F)(F)F)c1)C1(O)CCCCC1N1CC[C@H](N)C1.Cl.Cl

Reaction #57102

2-[(3S)-3-aminopyrrolidin-1-yl]-1-[3-(trifluoromethoxy)phenyl]ethylcyclohexanol Dihydrochloride

DOI: 10.6084/m9.figshare.5104873.v1

CN[C@H]1CCN(C2CCCCC2(O)C(C)c2cccc(C(F)(F)F)c2)C1.Cl.Cl

Reaction #57103

2-[(3S)-3-(methylamino)pyrrolidin-1-yl]-1-[3-(trifluoromethyl)phenyl]ethylcyclohexanol Dihydrochloride

DOI: 10.6084/m9.figshare.5104873.v1

CC(c1cccc(C(F)(F)F)c1)C1(O)CCCCC1N1CC[C@H](N(C)C)C1.Cl.Cl

Reaction #57104

2-[(3S)-3-(dimethylamino)pyrrolidin-1-yl]-1-[3-(trifluoromethyl)phenyl]ethylcyclohexanol Dihydrochloride

DOI: 10.6084/m9.figshare.5104873.v1

C#Cc1cccc(C(CN2CCN(C(=O)OC(C)(C)C)CC2)C2(O)CCCCC2)c1

Reaction #57114

tert-butyl 4-[2-(3-ethynylphenyl)-2-(1-hydroxycyclohexyl)ethyl]piperazine-1-carboxylate

収率 80.0%DOI: 10.6084/m9.figshare.5104873.v1

CC(C)(C)OC(=O)N1CCN(CC(c2ccccn2)C2(O)CCCCC2)CC1

Reaction #57117

tert-butyl 4-[2-(1-hydroxy-cyclohexyl)-2-pyridin-2-yl-ethyl]-piperazine-1-carboxylate

収率 78.0%DOI: 10.6084/m9.figshare.5104873.v1

Cl.Cl.N[C@@H]1CCN(CC(c2ccc3ccccc3c2)C2(O)CCCCC2)C1

Reaction #57119

1-[2-[(3R)-3-aminopyrrolidin-1-yl]-1-(2-naphthyl)ethyl]cyclohexanol Dihydrochloride

DOI: 10.6084/m9.figshare.5104873.v1

CN[C@@H]1CCN(CC(c2ccc3ccccc3c2)C2CCCCC2O)C1.Cl.Cl

Reaction #57120

2-[(3R)-3-(methylamino)pyrrolidin-1-yl-1-(2-naphthyl]ethyl}cyclohexanol Dihydrochloride

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

Cl.Cl.OC1(C(CN2CCNCC2)c2ccc(OCc3ccccc3C(F)(F)F)cc2)CCCCC1

Reaction #57128

1-[2-piperazin-1-yl-1-(4-{[2-(trifluoromethyl)benzyl]oxy}phenyl)ethyl]cyclohexanol Dihydrochloride

DOI: 10.6084/m9.figshare.5104873.v1

$C[C@]12CC[C@H]3[C@@H](C/C(=N\O)[C@@]4(O)CCCC[C@]34C)[C@@H]1CC13OCCOC12OCCO3$

Reaction #70382

17,17-Bis(ethylendioxy)-5α-hydroxy-6-(E)-hydroxyimino-androstane

収率 85.0%DOI: 10.6084/m9.figshare.5104873.v1

$C[C@]12CC[C@H]3[C@@H](C/C(=N\O)[C@@]4(O)CC(=O)CC[C@]34C)[C@@H]1CCC2=O$

Reaction #70383

収率 80.0%DOI: 10.6084/m9.figshare.5104873.v1

$CO/N=C1\C[C@H]2[C@@H]3CCC(=O)[C@@]3(C)CC[C@@H]2[C@@]2(C)CCC(=O)C[C@]12O$

Reaction #70384

収率 80.0%DOI: 10.6084/m9.figshare.5104873.v1

C[C@]12CCC(=O)C=C1/C(=N/O)C[C@@H]1[C@@H]2CC[C@]2(C)C(=O)CC[C@@H]12

Reaction #70412

収率 67.0%DOI: 10.6084/m9.figshare.5104873.v1

CC1=C[C@H]2[C@@]3(O)[C@H](C)[C@@H](O)[C@]4(O)[C@H]([C@@H]3C=C(CO)C[C@]2(O)C1=O)C4(C)C

Reaction #71613

DOI: 10.6084/m9.figshare.5104873.v1

CCOCc1nc2c(N)nc3ccccc3c2n1CCCC1(O)CCCCC1

Reaction #73006

1-{3-[4-amino-2-(ethoxymethyl)-1H-imidazo[4,5-c]quinolin-1-yl]propyl}cyclohexanol

収率 53.0%DOI: 10.6084/m9.figshare.5104873.v1

O=CNc1ccc(OC23CC4CC(CC(C4)C2)C3)cc1

Reaction #94369

N-Formyl-p-(1-adamantyloxy)aniline

DOI: 10.6084/m9.figshare.5104873.v1

Cc1cc(N2CCCC2)cc(C)c1OC12CC3CC(CC(C3)C1)C2

Reaction #94375

N-[4-(1-Adamantyloxy)-3,5-dimethylphenyl]-pyrrolidine

DOI: 10.6084/m9.figshare.5104873.v1

CC(C(=O)O)[C@]1(O)CCC[C@H](Nc2nc(-c3c[nH]c4ncc(F)cc34)ncc2F)C1

Reaction #162190

DOI: 10.6084/m9.figshare.5104873.v1

1 ページ次のページ