Substructure Search

Cl.Nc1ccccc1

Cl.Nc1cccc2c1ccc(=O)n2CCN1CCC(NCc2ccc3c(c2)OCCO3)CC1
Reaction #68216
1-(2-(4-((2,3-dihydro-1,4-benzodioxin-6-ylmethyl)amino)piperidin-1-yl)ethyl)-5-aminoquinolin-2(1H)-one hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CNc1cccc2c1ccc(=O)n2CCN1CCC(NCc2ccc3c(c2)OCCO3)CC1.Cl
Reaction #68220
1-(2-(4-((2,3-dihydro-1,4-benzodioxin-6-ylmethyl)amino)piperidin-1-yl)ethyl)-5-(N-methylamino)quinolin-2(1H)-one hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(c1)N(CCN1CCC(NCc3ccc4c(c3)OCCO4)CC1)C(=O)CC2.Cl
Reaction #68288
1-(2-(4-((2,3-dihydro-1,4-benzodioxin-6-ylmethyl)amino)piperidin-1-yl)ethyl)-7-methoxy-3,4-dihydroquinolin-2(1H)-one hydrochloride
Yield 135.8%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2ncc(=O)n(CCN3CCC(NCc4ccc5c(c4)NC(=O)CC5)CC3)c2c1.Cl
Reaction #68290
7-methoxy-1-(2-(4-((2-oxo-1,2,3,4-tetrahydroquinolin-7-ylmethyl)amino)piperidin-1-yl)ethyl)quinoxalin-2(1H)-one hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CCc1[nH]c(C(=O)Nc2ccc3c(c2)OCCN3Cc2cccc(C(=O)O)c2)nc1Cl
Reaction #71867
title compound
Yield 71.3%DOI: 10.6084/m9.figshare.5104873.v1
CCc1[nH]c(C(=O)Nc2ccc3c(c2)OCCN3Cc2ccc(C(=O)O)cc2)nc1Cl
Reaction #71871
title compound
Yield 101.7%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCN(C(=O)c1ccc2c(c1)nc(CNc1ccc(C(=N)N)cc1Cl)n2C)c1ccccc1.Cl
Reaction #78627
1-Methyl-2-[N-(4-amidino-2-chlorophenyl)aminomethyl]benzimidazol-5-yl-carboxylic acid-N-phenyl-N-(2-ethoxycarbonylethyl)amide hydrochloride
Yield 82.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(=O)n(-c2ccc(N3CCOCC3)c(Cl)c2)c(COc2ccc(Cl)c3ccccc23)n1
Reaction #84569
title compound
Yield 56.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C(=O)Nc1ccc(C(=O)O)cc1)n1ccc(-c2cc(Cl)ccc2Br)cc1=O
Reaction #85237
4-({2-[4-(2-Bromo-5-chlorophenyl)-2-oxopyridin-1(2H)-yl]propanoyl}amino)benzoic acid
DOI: 10.6084/m9.figshare.5104873.v1
Cl.Cl.O=C1CCCN1c1ccc(OCCCN(CCn2ccc3ccccc3c2=O)Cc2ccncc2)cc1
Reaction #156194
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2c(Oc3ccc(NC(=O)Nc4ccc(F)cc4F)c(Cl)c3)ccnc2cc1OCCN(C)CCO
Reaction #177766
DOI: 10.1039/C8SC04228D
CCCNC(=O)N(C(C)=O)c1ccc(Oc2ncnc3cc(OC)c(OC)cc23)cc1Cl
Reaction #182877
DOI: 10.1039/C8SC04228D
COc1cc(N)c(Cl)cc1C(=O)NCCCCN1CCC(CNC(=O)c2cc(Cl)c(N)cc2OC)C1
Reaction #183754
DOI: 10.1039/C8SC04228D
COc1ccc(C2Nc3c(OC)cccc3C(=O)N2c2ccc(OCCCl)cc2)cc1
Reaction #188172
DOI: 10.1039/C8SC04228D
COC(=O)c1cc2c(Oc3ccc(N)c(Cl)c3)ccnc2cc1OCc1ccccc1
Reaction #189573
DOI: 10.1039/C8SC04228D
CCN(C(=O)OC1CCCCC1)c1ccc(Oc2ncnc3cc(OC)c(OC)cc23)cc1Cl
Reaction #201490
DOI: 10.1039/C8SC04228D
COc1cc2nccc(Oc3ccc(NC(=S)NC(=O)c4cccc(Cl)c4)c(C)c3)c2cc1OC
Reaction #202253
DOI: 10.1039/C8SC04228D
COc1cc(-n2ccc3nc(-c4ccc(Cl)cc4)sc3c2=O)ccc1CCCN1CCCC1
Reaction #207326
DOI: 10.1039/C8SC04228D
COc1cc2c(Nc3ccc4nn[nH]c4c3)c(C#N)cnc2cc1OCCCl
Reaction #209094
DOI: 10.1039/C8SC04228D
O=C(c1ccc(CN2C(=O)CN(C(=O)c3ccc(Cl)cc3)Cc3ccccc32)cc1)N1CC=CC1
Reaction #222832
DOI: 10.1039/C8SC04228D
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