Substructure Search

37658

COc1ccc2c(C(=O)c3ccc(OCCN4CCCCC4)cc3)c(-c3cccc4ccccc34)sc2c1
Reaction #2287
title compound
Yield 58.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccc(OCCN2CCCCC2)cc1)c1c(-c2cccc3ccccc23)sc2cc(O)ccc12
Reaction #2288
title product
Yield 53.4%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(C(=O)c3ccc(OCCN4CCCCC4)cc3)c(-c3ccc4ccccc4c3)sc2c1
Reaction #2289
title compound
Yield 75.1%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(C(=O)c3ccc(OCCN4CCCCC4)cc3)c(-c3cccs3)sc2c1
Reaction #2291
title compound
Yield 72.1%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(Cc2sc3cc(OC)ccc3c2C(=O)c2ccc(OCCN3CCCCC3)cc2)cc1
Reaction #2292
title compound
Yield 29.4%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(-c2sc3cc(OC)ccc3c2C(=O)c2ccc(OCCN3CCCCC3)cc2)cc1.Cl
Reaction #2880
6-Methoxy-2-(4-methoxyphenyl)-3-[4-(2-piperidinoethoxy)benzoyl]-benzo[b]thiophene Hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
N#CNc1nccn1C1CCN(CC2CCc3ccccc3O2)CC1
Reaction #51614
[1-[1-[(3,4-dihydro-2H-1-benzopyran-2-yl)methyl]-4-piperidinyl]-1H-imidazol-2-yl]cyanamide
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1ccc2c(c1)OC(CN1CCCCC1)CC2
Reaction #67257
1-{[7-(METHYLSULFONYL)-3,4-DIHYDRO-2H-CHROMEN-2-YL]METHYL}PIPERIDINE
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(-c2sc3cc(OC)ccc3c2C(=O)c2ccc(OCCN3CCCCC3)cc2)cc1.Cl
Reaction #79143
6-Methoxy-2-(4-methoxyphenyl)-3-[4-(2-piperidinylethoxy)benzoyl]-benzo[b]thiophene Hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(-c2ccc(Cl)cc2)c2cc(OC(C)(C)C(=O)N3CCCCC3)ccc2n1C
Reaction #95189
2-[3-(4-Chlorophenyl)-1,2-dimethyl-1H-indole-5-yloxy]-2-methyl-propanoic acid piperidide
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1cc(F)c2c(c1)OC(CN1CCCCC1)OC2
Reaction #173030
DOI: 10.1039/C8SC04228D
COc1ccc2c(Oc3ccc(OCCN4CCCCC4)cc3)c(-c3ccc(S(C)=O)s3)ccc2c1
Reaction #174741
DOI: 10.1039/C8SC04228D
CC(C)(C)[Si](C)(C)Oc1ccc2c(c1)CCC(c1ccc(O[Si](C)(C)C(C)(C)C)cc1N(CCF)Cc1ccc(OCCN3CCCCC3)c(F)c1)C2
Reaction #175611
DOI: 10.1039/C8SC04228D
COc1ccc2c(C(=O)c3ccc(OCCN4CCCCC4)cc3)c(-c3c(F)cc(F)cc3F)ccc2c1
Reaction #177131
DOI: 10.1039/C8SC04228D
COc1c(Cl)c(C)c(C(C)=O)c(OCCN2CCCC(F)(F)C2)c1OCCC(C)c1ccc(F)cc1
Reaction #179702
DOI: 10.1039/C8SC04228D
COc1ccc2c(C(=O)c3ccc(OCCN4CCCCC4)cc3)c(-c3ccccc3C=O)sc2c1
Reaction #182601
DOI: 10.1039/C8SC04228D
CC1CCN(CCOc2ccc(NC(=O)C#Cc3ccc(C(F)(F)F)cc3Cl)cc2Cl)CC1
Reaction #184214
DOI: 10.1039/C8SC04228D
CC(Cc1ccc(OCCN2CCCCC2)cc1)(C(=O)O)S(=O)(=O)c1ccc(Br)cc1
Reaction #185643
DOI: 10.1039/C8SC04228D
COc1ccc2c(C(O)c3ccc(OCCN4CCCCC4)cc3)c(-c3ccccc3CO)ccc2c1
Reaction #185738
DOI: 10.1039/C8SC04228D
O=C(c1ccc(OCCN2CCCCC2)cc1)c1c(-c2ccccc2F)ccc2cc(OCc3ccccc3)ccc12
Reaction #186211
DOI: 10.1039/C8SC04228D
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