部分構造検索

9400

Cc1cc(C)c2c(c1O)C(NCC(O)CN1CCN(c3cccc(Cl)c3)CC1)C(C)(C)C2
Reaction #5100
1-{3-[4-(3-chlorophenyl)-1-piperazinyl]-2-hydroxypropylamino}-2,3-dihydro-7-hydroxy-2,2,4,6-tetramethyl-1H-indene
DOI: 10.6084/m9.figshare.5104873.v1
CNC(=O)c1ccnc(NCCCN2CCN(c3cccc(Cl)c3)CC2)n1.Cl
Reaction #5436
base
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(Cl)cc1N1CCN(CCCNc2nccc(C(=O)NCCNc3nc(=O)cc[nH]3)n2)CC1
Reaction #5437
2-[[3-(4-(5-Chloro-2-methoxyphenyl)piperazin-1-yl]propyl]amino]-N-[2-[(4-oxo-1,4-dihydropyrimidin-2-yl)amino]ethyl]pyrimidine-4-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(Cl)cc1N1CCN(CCNc2nccc(C(=O)NCCCNc3nc(=O)cc[nH]3)n2)CC1
Reaction #5438
2-[[2-[4-(5-Chloro-2-methoxyphenyl)piperazin-1-yl)ethyl]amino]-N-[3-[(4-oxo-1,4-dihydropyrimidin-2-yl)amino]propyl]pyrimidine-4-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(Cl)cc1N1CCN(CCNc2nccc(C(=O)N3CCC(Nc4nc(=O)cc[nH]4)CC3)n2)CC1
Reaction #5439
compound
収率 55.9%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Nc1cccc(CCN2CCN(c3cc(Cl)cc4nc(C)ccc34)CC2)c1.Cl.Cl
Reaction #44102
title compound
収率 65.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(Cl)cc1N1CCN(CCCNc2cnc(C(=O)NCCNC(=O)OC(C)(C)C)cn2)CC1
Reaction #65472
1,1-Dimethylethyl 2-[[[2-[[3-[4-(5-chloro-2-methoxyphenyl)piperazin-1-yl]propyl]amino]pyrazin-5-yl]carbonyl]amino]ethylcarbamate
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)COc1ccc(Cl)cc1N1CCN(S(=O)(=O)c2ccccc2)CC1
Reaction #66541
title product
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)COc1ccc(Cl)cc1N1CCN(S(=O)(=O)Cc2ccccc2)CC1
Reaction #66542
sub-title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)COc1ccc(Cl)cc1N1CCN(C(=O)Cc2ccccc2)CC1
Reaction #66543
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(Cl)cc1N1CCN(CCN2C(=O)CC3(CCCC3)CC2=O)CC1
Reaction #77305
title compound
収率 49.4%DOI: 10.6084/m9.figshare.5104873.v1
OCCCN1CCN(c2ccc(Cl)c(Cl)c2)CC1
Reaction #92496
compound 7p
DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccccc2C(=O)N1CCCN1CCN(c2cccc(Cl)c2Cl)CC1
Reaction #162664
title compound
収率 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
収率 40.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCN2c3cc(Cl)c(Cl)cc3NCCC2C1
Reaction #167680
tert-butyl 9,10-dichloro-1,2,4a,5,6,7-hexahydrobenzo[b]pyrazino[1,2-d][1,4]diazepine-3(4H)-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CCNC(=O)N1C(=O)CCc2ccc(OCCCCN3CCN(c4cccc(Cl)c4Cl)CC3)cc21
Reaction #180052
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CCN(c2cccc(Cl)c2)C(C(=O)NCCN2CCOCC2)C1
Reaction #182747
DOI: 10.1039/C8SC04228D
Cc1c(O)cc(Cl)cc1N1CCN(C(=O)OC(C)(C)C)CC1
Reaction #191528
DOI: 10.1039/C8SC04228D
Cc1c(C)c2ccc(OCCCCN3CCN(c4cccc(Cl)c4Cl)CC3)nc2[nH]c1=O
Reaction #195300
DOI: 10.1039/C8SC04228D
CCCCCCCCCCCCCCCC(=O)OCOC(=O)N1C(=O)CCc2ccc(OCCCCN3CCN(c4cccc(Cl)c4Cl)CC3)cc21
Reaction #196487
DOI: 10.1039/C8SC04228D
1 ページ次のページ