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765047

COc1cc(NC(=S)OCCCN2CCN(c3ccccc3Cl)CC2)cc(OC)c1OC.Cl
Reaction #5954
title compound
Выход 42.6%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(c2c(Cl)cc3c([nH]c4cnccc43)c2NC(=O)c2cccnc2Cl)CC1
Reaction #40464
desired compound
Выход 25.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2ccc(S(=O)(=O)N[C@@H](CCCNC(=N)N)C(=O)N3CCN(c4ccccc4Cl)CC3)cc2c1
Reaction #63274
1-[N2 -(7-methoxy-2-naphthalenesulfonyl)-L-arginyl]-4-(2-chlorophenyl)piperazine
Выход 28.0%DOI: 10.6084/m9.figshare.5104873.v1
O=c1ccc2ccc(OCCCCN3CCN(c4cccc(Cl)c4Cl)CC3)cc2[nH]1
Reaction #71515
desired product
Выход 102.3%DOI: 10.6084/m9.figshare.5104873.v1
CCCC(=O)OCN1C(=O)CCc2ccc(OCCCCN3CCN(c4cccc(Cl)c4Cl)CC3)cc21
Reaction #71516
Compound 2B
Выход 95.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCC(=O)OCn1c(=O)ccc2ccc(OCCCCN3CCN(c4cccc(Cl)c4Cl)CC3)cc21
Reaction #71517
Compound 2
Выход 63.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(N1CCCC(CN2CCN(c3ccccc3Cl)CC2)C1)C1(c2ccc(Cl)cc2)CCC1
Reaction #78927
7
Выход 42.0%DOI: 10.6084/m9.figshare.5104873.v1
Cl.Fc1ccc2c(CCCN3CCN(c4ccccc4Cl)CC3)noc2c1
Reaction #92893
product
Выход 139.6%DOI: 10.6084/m9.figshare.5104873.v1
Cl.Fc1ccc2c(CCCN3CCN(c4ccccc4Cl)CC3)noc2c1
Reaction #93152
product
Выход 139.6%DOI: 10.6084/m9.figshare.5104873.v1
CCNC(=O)c1ccc(N2CCN(Cc3cnc4c(c3)NC(=O)[C@@H]3CSCCN43)CC2)c(Cl)c1
Reaction #156875
product
Выход 26.0%DOI: 10.6084/m9.figshare.5104873.v1
CNC(=O)c1ccc(N2CCN(Cc3cnc4c(c3)NC(=O)[C@@H]3CSCCN43)CC2)c(Cl)c1
Reaction #156877
product
Выход 11.2%DOI: 10.6084/m9.figshare.5104873.v1
CCNC(=O)c1ccc(N2CCN(Cc3cnc4c(c3)NC(=O)[C@@H]3CCCCN43)CC2)c(Cl)c1
Reaction #156878
product
Выход 41.8%DOI: 10.6084/m9.figshare.5104873.v1
CNC(=O)c1ccc(N2CCN(Cc3cnc4c(c3)NC(=O)[C@@H]3CCCCN43)CC2)c(Cl)c1
Reaction #156879
product
Выход 29.0%DOI: 10.6084/m9.figshare.5104873.v1
CCNC(=O)c1ccc(N2CCN(Cc3cnc4c(c3)NC(=O)[C@@H]3CCCN43)CC2)c(Cl)c1
Reaction #156908
(S)-3-chloro-N-ethyl-4-(4-((6-oxo-5,6,6a,7,8,9-hexahydropyrido[3,2-e]pyrrolo[1,2-a]pyrazin-3-yl)methyl)piperazin-1-yl)benzamide
Выход 35.3%DOI: 10.6084/m9.figshare.5104873.v1
CNC(=O)c1ccc(N2CCN(Cc3cnc4c(c3)NC(=O)[C@@H]3CCCN43)CC2)c(Cl)c1
Reaction #156924
(S)-3-chloro-N-methyl-4-(4-((6-oxo-5,6,6a,7,8,9-hexahydropyrido[3,2-e]pyrrolo[1,2-a]pyrazin-3-yl)methyl)piperazin-1-yl)benzamide
Выход 25.7%DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccccc2C(=O)N1CCCN1CCN(c2cccc(Cl)c2Cl)CC1
Reaction #162664
title compound
Выход 80.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc(C(=O)NCC(O)CN2CCN(c3cccc(Cl)c3Cl)CC2)c(C)n1-c1ccccc1
Reaction #162675
title compound
Выход 40.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(N1CCCC(CN2CCN(c3ccccc3Cl)CC2)C1)C1(c2ccc(Cl)cc2)CCC1
Reaction #179112
DOI: 10.1039/C8SC04228D
CCNC(=O)N1C(=O)CCc2ccc(OCCCCN3CCN(c4cccc(Cl)c4Cl)CC3)cc21
Reaction #180052
DOI: 10.1039/C8SC04228D
CC(=O)OCOC(=O)N1C(=O)CCc2ccc(OCCCCN3CCN(c4cccc(Cl)c4Cl)CC3)cc21
Reaction #183174
DOI: 10.1039/C8SC04228D
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