Busqueda de Subestructura

CC1(CCNCC1)O

C[C@H](OC(=O)[C@@H](c1ccccc1)N1CCC(C)(O)CC1)c1ccccc1
Reaction #46638
title compound
Rendimiento 60.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(O)CCN([C@@H](C(=O)O)c2ccccc2)CC1
Reaction #46639
title compound
Rendimiento 98.7%DOI: 10.6084/m9.figshare.5104873.v1
Cc1[nH]c2ccccc2c1CCC(=O)N1CCC(O)(Cc2ccccc2)CC1
Reaction #54452
1-[β-(2-methyl-3-indolyl)propionyl]-4-benzyl-4-hydroxypiperidine
DOI: 10.6084/m9.figshare.5104873.v1
OC1(c2cnc3c(NCc4nnc5ccc(-c6cc(F)cc(F)c6)nn45)ccnc3c2)CCNCC1
Reaction #68675
4-(8-((6-(3,5-difluorophenyl)-[1,2,4]triazolo[4,3-b]pyridazin-3-yl)methylamino)-1,5-naphthyridin-3-yl)piperidin-4-ol
DOI: 10.6084/m9.figshare.5104873.v1
CC(Nc1ncc(C#N)c(-c2c[nH]c3ncc(C(F)(F)F)cc23)n1)c1ccc(C2(O)CCN(C)CC2)nc1
Reaction #69134
title compound
Rendimiento 9.4%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)N1CCC(O)(c2ccc(Br)cc2)CC1
Reaction #69981
4-(4-bromophenyl)-1-(methanesulphonyl)piperidin-4-ol
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CN(C(=O)[C@@H]2CC[C@@H]2N)CC[C@]1(O)c1ccc(Cl)cc1.Cl
Reaction #70830
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Clc1ccc(C2(c3ccc(Br)cc3)CCNCC2)cc1
Reaction #73775
title compound
Rendimiento 203.1%DOI: 10.6084/m9.figshare.5104873.v1
O=c1[nH]c2ccc(Cl)cc2n1CCCN1CCC(O)(c2ccc(Cl)cc2)CC1
Reaction #75166
6-chloro-1-{3-[4-(4-chlorophenyl)-4-hydroxy-1-piperidinyl]propyl}-1,3-dihydro-2H-benzimidazol-2-one
DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)C1(O)CCN(Cc2ccccc2)CC1
Reaction #75591
1-benzyl-4-hydroxy-4-piperidine carboxamide
Rendimiento 68.8%DOI: 10.6084/m9.figshare.5104873.v1
CCCCOc1ccc(NC(=O)CC2(O)CCN(Cc3ccccc3)CC2)cc1
Reaction #78239
titled compound
Rendimiento 24.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCOc1ccc(N(C)CC2(O)CCN(Cc3ccccc3)CC2)cc1
Reaction #78240
titled compound
Rendimiento 75.5%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-c2ccncc2)c(C(=O)N2CCC(O)(Cc3ccccc3)CC2)c1
Reaction #88850
title compound
Rendimiento 64.6%DOI: 10.6084/m9.figshare.5104873.v1
Cc1noc(-c2ccncc2)c1C(=O)N1CCC(O)(Cc2ccccc2)CC1
Reaction #88852
title compound
Rendimiento 62.8%DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1c(Br)ccc2c1OCO2)N1CCC(O)(Cc2ccccc2)CC1
Reaction #88858
title compound
Rendimiento 99.6%DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccccc1-c1ccncn1)N1CCC(O)(Cc2ccccc2)CC1
Reaction #88863
title compound
Rendimiento 34.9%DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1cccnc1-c1ccncc1)N1CCC(O)(Cc2ccccc2)CC1
Reaction #88873
title compound
Rendimiento 46.8%DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1cccnc1-c1ccncn1)N1CCC(O)(Cc2ccccc2)CC1
Reaction #88875
title compound
Rendimiento 25.9%DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccccc1-c1cnco1)N1CCC(O)(Cc2ccccc2)CC1
Reaction #88880
title compound
Rendimiento 48.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)CCN1CCC(O)(c2ccccc2)CC1.Cl
Reaction #94242
4-(4-hydroxy-4-phenypiperidino)-2-butanone hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
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