Busqueda de Subestructura

CN1CCCCC1

CC(=O)Nc1ccc(C(=O)N(CCN2CCC(C(=O)c3ccc(F)cc3)CC2)c2cccc(C(F)(F)F)c2)cc1
Reaction #2582
title compound
Rendimiento 101.4%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCC(O)(c2cnc3ccccc3c2)CC1
Reaction #5063
expected product
Rendimiento 53.8%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(NC(=O)C(C)(C)NC(=O)c2ccc(Cl)s2)ccc1C(=O)N1CCCCC1CCCO
Reaction #43386
5-chloro-thiophene-2-carboxylic acid-N-{1-methyl-1-[3-methyl-4-(2-{3-hydroxy-prop-1-yl}-piperidin-1-yl-carbonyl)-phenylcarbamoyl]-ethyl}-amide
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCC(C)(C)c1ccc(C2CN(Cc3ccccc3)CCC2(O)CCCc2ccccc2)c(OCc2ccccc2)c1
Reaction #54346
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCC(C)(C)c1ccc(C2=C(CCCc3ccccc3)CCN(Cc3ccccc3)C2)c(OCc2ccccc2)c1
Reaction #54347
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCC(C)(C)c1ccc(C2CNCCC2(O)CCCc2ccccc2)c(O)c1
Reaction #54348
title compound
DOI: 10.6084/m9.figshare.5104873.v1
c1cc(OCCCN2CCCCC2)ncc1CN1CCCCC1
Reaction #58740
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(OCCCN2CCCCC2)no1
Reaction #58762
product
Rendimiento 192.6%DOI: 10.6084/m9.figshare.5104873.v1
OCCCN1CCCCC1
Reaction #61969
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CN1CCC(O)(c2ccc(C3(C)OCCO3)cn2)CC1
Reaction #69133
title compound
Rendimiento 85.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCC(O)(c2ccc3c(c2)CN(C(=O)OC(C)(C)C)C3)CC1
Reaction #69716
5-(4-hydroxy-1-methyl-piperidin-4-yl)-1,3-dihydro-isoindole-2-carboxylic acid tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CN1CCC(O)(c2ccc3c(c2)CN(C(c2ccccc2)(c2ccccc2)c2ccccc2)C3)CC1
Reaction #69748
1-methyl-4-(2-trityl-2,3-dihydro-1H-isoindol-5-yl)-piperidin-4-ol
Rendimiento 57.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1N(Cc2cccc(-n3nccn3)c2)CCCC12CCN(c1cnc3ccccc3n1)CC2
Reaction #69849
title compounds
Rendimiento 30.9%DOI: 10.6084/m9.figshare.5104873.v1
O=C1N(Cc2ccccc2-n2nccn2)CCCC12CCN(c1cnc3ccccc3n1)CC2
Reaction #69856
title compound
Rendimiento 66.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCC(O)(C[N+](=O)[O-])CC1
Reaction #73066
1-methyl-4-nitromethylpiperidin-4-ol
Rendimiento 73.4%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCC(N2CCC(n3cc(I)c4c(Cl)ncnc43)CC2)CC1
Reaction #79894
4-chloro-5-iodo-7-[1-(1-methyl-4-piperidinyl)-4-piperidinyl]-7H-pyrrolo[2,3-d]pyrimidine
Rendimiento 61.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCCCC1CN1C[C@H](CCCB(O)O)[C@](N)(C(=O)O)C1
Reaction #89659
(3R,4S)-3-amino-4-(3-boronopropyl)-1-((1-methylpiperidin-2-yl)methyl)pyrrolidine-3-carboxylic acid
Rendimiento 74.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCC(NC2CCCN(c3ccncc3NC(=O)c3nc(Br)cnc3N)C2)CC1
Reaction #157072
3-amino-6-bromo-N-(4-(3-(1-methylpiperidin-4-ylamino)piperidin-1-yl)pyridin-3-yl)pyrazine-2-carboxamide
Rendimiento 66.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1CC=C(O[Si](C)(C)C)CC1
Reaction #160376
1-methyl-4-trimethylsilanyloxy-1,2,3,6-tetrahydro-pyridine
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)c1nnc2ccc(O[C@@H]3CC[C@H](NC(=O)Nc4cc(C(C)(C)C)nn4-c4cccc(OCCN5CCC(O)CC5)c4)c4ccccc43)cn12.O=CO
Reaction #162787
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Página 1Siguiente