部分構造検索

1125907

Cl.N=C(NCCCCc1ccc(O)cc1)NC(=O)c1nc(Cl)c(N)nc1N
Reaction #53369
4-(4-Hydroxyphenyl)butylamidino-3,5-diamino-6-chloropyrazinecarboxamide hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
Cl.N=C(NCCCCc1ccc(O)cc1)NC(=O)c1nc(Cl)c(N)nc1N
Reaction #53374
5
収率 84.4%DOI: 10.6084/m9.figshare.5104873.v1
Cl.N=C(NCCCc1ccc(O)cc1)NC(=O)c1nc(Cl)c(N)nc1N
Reaction #53377
compound 15
収率 60.0%DOI: 10.6084/m9.figshare.5104873.v1
Cl.N=C(NCCCCCc1ccc(O)cc1)NC(=O)c1nc(Cl)c(N)nc1N
Reaction #53380
22
収率 131.5%DOI: 10.6084/m9.figshare.5104873.v1
Cl.N=C(NCCCCc1ccc(O)c(O)c1)NC(=O)c1nc(Cl)c(N)nc1N
Reaction #53384
compound 28
収率 51.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CCCCNC(=N)NC(=O)c2nc(Cl)c(N)nc2N)c(OC)c1.Cl
Reaction #53390
compound 80
収率 181.3%DOI: 10.6084/m9.figshare.5104873.v1
Cl.N=C(NCCCCc1ccc(CC(=O)O)cc1)NC(=O)c1nc(Cl)c(N)nc1N
Reaction #53395
9
収率 46.5%DOI: 10.6084/m9.figshare.5104873.v1
Cl.N=C(NCCCCc1ccc(O)cc1)NC(=O)c1nc(Cl)c(N)nc1N
Reaction #53407
5
収率 84.4%DOI: 10.6084/m9.figshare.5104873.v1
Cl.N=C(NCCCCc1ccc(CO)cc1)NC(=O)c1nc(Cl)c(N)nc1N
Reaction #53411
68
収率 194.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCNC(=N)NC(=O)c1nc(Cl)c(N)nc1N.Cl
Reaction #53420
compound 116
収率 194.0%DOI: 10.6084/m9.figshare.5104873.v1
Cl.N=C(NCCCCc1ccc(CC(=O)O)cc1)NC(=O)c1nc(Cl)c(N)nc1N
Reaction #168478
9
収率 46.5%DOI: 10.6084/m9.figshare.5104873.v1
Cl.N=C(NCCCCc1ccc(O)cc1)NC(=O)c1nc(Cl)c(N)nc1N
Reaction #168488
5
収率 84.4%DOI: 10.6084/m9.figshare.5104873.v1
Cl.N=C(NCCCCc1ccc(CO)cc1)NC(=O)c1nc(Cl)c(N)nc1N
Reaction #168492
68
収率 194.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NCCOc1ccc(CCCCNC(N)=NC(=O)c2nc(Cl)c(N)nc2N)cc1
Reaction #168504
pure product
収率 92.5%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1OC[C@@H](O)[C@H](CN(CCOc2ccc(CCCCNC(=N)NC(=O)c3nc(Cl)c(N)nc3N)cc2)C[C@@H]2O[C@H](C)OC[C@H]2O)O1
Reaction #168508
11
収率 73.4%DOI: 10.6084/m9.figshare.5104873.v1
NCCCCc1ccccc1OC[C@H](O)CO
Reaction #168509
compound 70
収率 49.0%DOI: 10.6084/m9.figshare.5104873.v1
Cl.N=C(N)N(CCCCc1ccc(C(=O)NCCO)cc1)C(=O)c1nc(Cl)c(N)nc1N
Reaction #168518
29
収率 79.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)COc1ccc(CCCCNC(N)=NC(=O)c2nc(Cl)c(N)nc2N)cc1
Reaction #168520
49
収率 57.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)[C@H](NS(=O)(=O)c1ccc(CCCCNC(N)=NC(=O)c2nc(Cl)c(N)nc2N)cc1)C(N)=O
Reaction #219737
desired product
収率 54.0%DOI: 10.6084/m9.figshare.5104873.v1
NC(=NC(=O)c1nc(Cl)c(N)nc1N)NCCCCc1ccc(OCC(=O)Nc2ccccc2)cc1
Reaction #219740
2-(4-{4-[N′-(3,5-diamino-6-chloro-pyrazine-2-carbonyl)guanidino]butyl}phenoxy)-N-phenylacetamide
収率 67.1%DOI: 10.6084/m9.figshare.5104873.v1
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