部分構造検索

1130238

CS(=O)(=O)c1ccc(Oc2cc3nc(-c4ccccn4)[nH]c3cc2C2CCCN2C(N)=O)cc1
Reaction #41562
compound
DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)N1CCCC1c1cc2[nH]c(-c3ccccn3)nc2cc1Oc1ccc(F)cc1
Reaction #41563
compound
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #44510
compound
収率 86.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CCC1C(=O)NC(=O)N1C1CCN(C(=O)OCc2ccccc2)CC1
Reaction #48362
title compound
収率 80.5%DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)N(O)Cc1ccc(OCCc2noc(-c3ccccc3)n2)cc1
Reaction #50647
solid
収率 70.0%DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)NCc1ccc(N2CC(CNC(=O)c3ccc(Cl)s3)OC2=O)cc1
Reaction #69365
N-{[3-(4-{[(Aminocarbonyl)amino]methyl}phenyl)-2-oxo-1,3-oxazolidin-5-yl]-methyl}-5-chloro-2-thiophenecarboxamide
DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)c1nccc(Cl)c1Cl
Reaction #70996
3,4-dichloropicolinamide
収率 39.0%DOI: 10.6084/m9.figshare.5104873.v1
CO[C@@H]1CN(C(N)=O)CC[C@@H]1NC(=O)OCc1ccccc1
Reaction #71879
title compound
収率 81.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CC[C@@H](NC(N)=O)C1
Reaction #85819
crude title compound
DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)NC[C@@H]1CCN(c2nc(-c3ccc(N4CCOCC4)cc3)cc3nccnc23)C1
Reaction #85889
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc2c(OCC3CCCCC3)cccn2c1C(=O)N[C@H]1CCCN(C(N)=O)C1.Cl
Reaction #92745
N-[(3S)-1-carbamoylpiperidin-3-yl]-8-(cyclohexylmethoxy)-2-methylimidazo[1,2-a]pyridine-3-carboxamide hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)NCc1ccc(N2CC(CNC(=O)c3ccc(Cl)s3)OC2=O)cc1
Reaction #155657
N-{[3-(4-{[(Aminocarbonyl)amino]methyl}phenyl)-2-oxo-1,3-oxazolidin-5-yl]-methyl}-5-chloro-2-thiophenecarboxamide
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(N[C@@H]2CCN(C(=O)NC3CC4CCC(C3)N4C(N)=O)C2)nc1
Reaction #159327
3-((R)-3-(5-cyanopyridin-2-ylamino)pyrrolidine-1-carboxamido)-8-azabicyclo[3.2.1]octane-8-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)N1CCC1Nc1nc(-c2c[nH]c3ncc(Cl)cc23)ncc1F
Reaction #162065
512
収率 79.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](Nc1cc(N2CCC(N3CCC(NC(N)=O)C3)CC2)ccc1Cl)c1ccc(Cl)cc1Cl
Reaction #162322
desired product
収率 26.0%DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)N1CCC(CCCNc2ncc(Cl)c(-c3cc4c(C(=O)NC5CC5)cccc4s3)n2)CC1
Reaction #172986
DOI: 10.1039/C8SC04228D
CC(c1ccc2c(c1)Sc1cc(Cl)ccc1O2)N(O)C(N)=O
Reaction #177408
DOI: 10.1039/C8SC04228D
NC(=O)N(O)Cc1ccc(N2CCC3(CC2)OCCO3)cc1
Reaction #178338
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)NCCC1CCCN(C(N)=O)C1
Reaction #187207
DOI: 10.1039/C8SC04228D
Cc1ccccc1N1CCCC2c3c(cccc3C(N)=O)CCC21
Reaction #195395
DOI: 10.1039/C8SC04228D
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