部分構造検索

CNCCN(C)C

CC(=O)Nc1ccc(C(=O)N(CCN2CCC(C(=O)c3ccc(F)cc3)CC2)c2ccccc2C(F)(F)F)cc1
Reaction #2581
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccccc1N(CCN1CCC(C(=O)c2ccc(F)cc2)CC1)C(=O)c1ccc(CNS(C)(=O)=O)cc1
Reaction #2600
title compound
収率 57.5%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccccc1N(CCN1CCC(C(=O)c2ccc(F)cc2)CC1)C(=O)c1ccc(NS(C)(=O)=O)cc1
Reaction #2601
title compound
収率 50.7%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ccc(C(=O)N(CCN2CCC(C(=O)c3ccc(F)cc3)CC2)c2cccnc2)cc1)c1ccccc1
Reaction #2615
title compound
収率 71.3%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-n2nccn2)c(C(=O)N2CCC[C@@H](C)[C@H]2CNc2ncc3ccccc3n2)c1
Reaction #89436
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-n2nccn2)c(C(=O)N2CCC[C@@H](C)[C@H]2CNc2ncc(C(F)(F)F)cn2)c1F
Reaction #89531
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cl
Reaction #187513
DOI: 10.1039/C8SC04228D
CC(C)N1CCC(Oc2cc3cc(C(=O)N4CCN(C(=O)C5CC5)CC4)[nH]c3cc2Br)CC1
Reaction #188624
DOI: 10.1039/C8SC04228D
CC(=O)N1CCN(C(=O)c2cc3cc(OC4CCN(C(C)C)CC4)ccc3n2C(C)C)CC1
Reaction #190962
DOI: 10.1039/C8SC04228D
COc1cc(N2CCN(C(=O)Cn3nc(C(F)(F)F)c(Cl)c3-c3ccc(C(F)(F)F)cc3)CC2)ccc1Cl
Reaction #194841
DOI: 10.1039/C8SC04228D
CC(=O)Nc1ccc(CN2CCN(C(=O)c3cc(C(F)(F)F)cc(C(F)(F)F)c3)C(Cc3ccc(Cl)c(Cl)c3)C2)cc1
Reaction #196589
DOI: 10.1039/C8SC04228D
CS(=O)(=O)Nc1ccc(-n2c(C(=O)N3CCC(F)(F)CC3)cc3cc(C(=O)N4CCN(C5CCC5)CC4)ccc32)cc1
Reaction #199337
DOI: 10.1039/C8SC04228D
CCN(CC)C(=O)N1CCN(C(=O)c2cc3cc(OC4CCN(C(C)C)CC4)ccc3[nH]2)CC1
Reaction #199979
DOI: 10.1039/C8SC04228D
CN1CCN(c2cccc(C3Nc4ccc(C(=O)NS(C)(=O)=O)cc4CC3(C)C)c2)C(=O)C1=O
Reaction #204618
DOI: 10.1039/C8SC04228D
COC(=O)NCC1CCC(C(=O)N2CC(c3ccc(F)cc3)C(N(C)C(=O)N(C)c3cc(C(F)(F)F)cc(C(F)(F)F)c3)C2)CC1
Reaction #205365
DOI: 10.1039/C8SC04228D
CNC(=O)C1CN(CC(=O)Nc2c(Cl)cc(C(C)=O)cc2Cl)CCN1CCCCN(c1ccc(F)cc1)c1ccc(F)cc1
Reaction #208901
DOI: 10.1039/C8SC04228D
CC(C)(C)c1cc(NC(=O)Nc2ccc(C(=O)N3CCN(Cc4ccc(C(O)(C(F)(F)F)C(F)(F)F)cc4)CC3)cc2F)no1
Reaction #209445
DOI: 10.1039/C8SC04228D
CN(Cc1ccc(Cl)c(Cl)c1)C1CC(C(=O)N2CCN(c3ccccc3C#N)CC2)N(Cc2ccccc2)C1
Reaction #210349
DOI: 10.1039/C8SC04228D
COc1cc(OC2CCN(S(=O)(=O)CCNC3CC3)CC2)ccc1CC(=O)N1CCN(c2ccccc2C)CC1C(N)=O
Reaction #215778
1-(2-methoxy-4-(1-(2-(N-cyclopropylamino)ethylsulfonyl)-4-piperidyloxy)phenylacetyl)-4-(2-methylphenyl)piperazine-2-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(c2c(F)c(NC(=O)C(C)(C)C)c3c(=O)cc(-c4ccc(NC(=O)C(C)(C)C)c(F)c4)oc3c2F)CC1
Reaction #221296
DOI: 10.1039/C8SC04228D
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