子结构搜索

Cc1cccc(N2CCNCC2)c1C

COc1ccc(N2CCN(C)CC2)c2c1CCN(C(=O)Cc1ccc(N3CCCCC3)cc1)C2
Reaction #708
收率 0.0%
COc1cc2oc(=O)c3c(c2cc1OCCCN1CCN(c2cccc(C)c2C)CC1)CCC3
Reaction #50624
8-{3-[4-(2,3-dimethylphenyl)-1-piperazinyl]propoxy}-2,3-dihydro-7-methoxy-cyclopenta[c][1]benzopyran-4(1H)-one
收率 84.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CN2C(=O)c3cccc(N4C[C@@H](C)N(Cc5ccccc5)[C@@H](C)C4)c3C2=O)cc1OC
Reaction #70601
Compound 42
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CN2C(=O)c3cccc(N4CC5CCC(C4)N5C(C)c4ccccc4)c3C2=O)cc1OC
Reaction #70602
title Compound 32
收率 38.5%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CN2C(=O)c3c(C=CS(C)(=O)=O)ccc(N4CCN([C@H](C)c5ccccc5)CC4)c3C2=O)cc1OC
Reaction #70603
Compound 62
收率 19.4%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C(CCCN)N2C(=O)c3cccc(N4CCN([C@H](C)c5ccccc5)CC4)c3C2=O)cc1OC
Reaction #70604
Compound 66
收率 10.4%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C(CCCNS(=O)(=O)c2cccs2)N2C(=O)c3cccc(N4CCN([C@H](C)c5ccccc5)CC4)c3C2=O)cc1OC
Reaction #70605
Compound 68
收率 35.6%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc([C@@H](CCCNS(=O)(=O)c2cccs2)N2C(=O)c3cccc(N4CCN(Cc5ccoc5)CC4)c3C2=O)cc1OC
Reaction #70606
Compound 170
收率 64.4%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc([C@@H](CCCNS(=O)(=O)c2cccs2)N2C(=O)c3cccc(N4CCN(C5CCCC5)CC4)c3C2=O)cc1OC
Reaction #70607
Compound 193
收率 48.8%DOI: 10.6084/m9.figshare.5104873.v1
Br.Cc1ccc(N2CCN(C)CC2)c2c1CC[C@@H](NC(=O)c1ccc(N3CCOCC3)cc1)C2
Reaction #77234
(R)-N-[5-methyl-8-(4-methylpiperazin-1-yl)-1,2,3,4-tetrahydro-2-naphtyl]-4-morpholinobenzamide monohydrobromide
收率 92.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCOc1ccc(C(=O)NC2CCc3c(O)ccc(N4CCN(C)CC4)c3C2)cc1
Reaction #175718
DOI: 10.1039/C8SC04228D
Cc1cccc(N2CCN(CCCc3cc(-c4ccccc4)n(C(C)(C)C)n3)CC2)c1C
Reaction #176677
DOI: 10.1039/C8SC04228D
Cc1cccc(N2CCN(CCCc3cc(-c4ccc(F)cc4)n(C(C)(C)C)n3)CC2)c1C
Reaction #177705
DOI: 10.1039/C8SC04228D
CN1CCN(c2cccc3c2CC(NC(=O)Cc2ccccc2)CC3)CC1
Reaction #180696
DOI: 10.1039/C8SC04228D
CN1CCN(c2cccc3c2CC(NC(=O)c2ccc(-c4ccc(O)cc4)cc2)CC3)CC1
Reaction #180802
DOI: 10.1039/C8SC04228D
CN1CCN(c2cccc3c2CC(NC(=O)c2ccc(C(=O)N4CCOCC4)cc2)CC3)CC1
Reaction #182048
DOI: 10.1039/C8SC04228D
COc1ccc(N2CCN(C)CC2)c2c1CCC(C(=O)Nc1ccc(N3CCOCC3)cc1)C2
Reaction #182693
DOI: 10.1039/C8SC04228D
O=C1CCc2cccc(N3CCN(CCCCOc4ccc5ccc(=O)[nH]c5n4)CC3)c2C1
Reaction #185995
DOI: 10.1039/C8SC04228D
O=C(Nc1ccc(Cl)cc1)c1cccn(C2CCc3c2cccc3N2CCNCC2)c1=O
Reaction #188053
DOI: 10.1039/C8SC04228D
CCc1cc(NC(=O)N2CCN(c3c(C)c(C)cc(C)c3C)CC2)c(OC)nc1C
Reaction #193367
DOI: 10.1039/C8SC04228D
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