Substructure Search

9787

COC(=O)c1cncn1C1CCCc2ccccc21
Reaction #5863
1-(1,2,3,4-Tetrahydronaphthalen-1-yl)-5-imidazolecarboxylic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CCN(CC)CCCOc1ccc([N+](=O)[O-])c(N)c1
Reaction #8146
2-nitro-5-(3-diethylamino-1-propoxy)aniline
DOI: 10.6084/m9.figshare.5104873.v1
Nc1nc(O)cc(C2CCCN(C(=O)OCc3ccccc3)C2)n1
Reaction #44706
Benzyl 3-(2-amino-6-hydroxypyrimidin-4-yl)piperidine-1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-c2csc3c(C(=O)NCC(OC)OC)cnc(N)c23)ccc1NC(=O)c1cc2ccccc2n1C
Reaction #45486
title compound
Yield 71.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-c2csc3c(/C=C/CCN4CCC(N)CC4)cnc(N)c23)ccc1NC(=O)c1cc2ccccc2n1C
Reaction #45493
title compound
Yield 33.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-c2csc3c(/C=C/CCN4CCC(CN)CC4)cnc(N)c23)ccc1NC(=O)c1cc2ccccc2n1C
Reaction #45494
title compound
Yield 30.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1=C(C(=O)NCCC(c2ccccc2)c2ccccc2)C(c2cccc(Cl)c2)N=C(N)N1
Reaction #52901
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C1NC(=O)C2(C=CC=C3OCC=C32)N1
Reaction #54241
spiro[cyclohexa(b)furan-4,4'-imidazolidine]-2', 5'-dione
DOI: 10.6084/m9.figshare.5104873.v1
CCCC(C)C1(CC)NC(=O)NC1=O
Reaction #54850
5-sec-amyl-5-ethylhydantoin
Yield 94.0%DOI: 10.6084/m9.figshare.5104873.v1
CCC1(c2ccccc2)NC(=O)NC1=O
Reaction #55078
5-ethyl-5-phenyl-hydantoin
Yield 66.0%DOI: 10.6084/m9.figshare.5104873.v1
CCC1(c2ccccc2)NC(=O)NC1=O
Reaction #56447
5-ethyl-5-phenyl-hydantoin
Yield 66.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C2NC(=O)NC2=O)cc1OC1CC2CCC1C2
Reaction #64748
hydantoin
Yield 71.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1NC(=O)C2(C=COc3c2ccc2cccnc32)N1
Reaction #75335
spiro[imidazolidin-4,4'-pyrano[3,2-h]quinolin]-2,5-dione
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCN(C(=O)c1cnc2c(c1)nc(CCc1ccc(C(=N)N)cc1)n2C)c1ccccn1.Cl
Reaction #78472
3-Methyl-2-[2-(4-amidinophenyl)ethyl]imidazo[4,5-b]pyridin-6-yl-carboxylic acid-N-(2-pyridyl)-N-(2-methoxycarbonylethyl)amide hydrochloride
Yield 75.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CN(C(=O)c1cnc2c(c1)nc(CCc1ccc(C(=N)N)cc1)n2C)c1ccccc1.Cl
Reaction #78473
3-Methyl-2-[2-(4-amidinophenyl)ethyl]imidazo[4,5-b]pyridin-6-yl-carboxylic acid-N-phenyl-N-ethoxycarbonylmethylamide hydrochloride
Yield 84.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1Cc2ccccc2N1C(=O)c1cnc2c(c1)nc(CCc1ccc(C(=N)N)cc1)n2C.Cl
Reaction #78475
2-[2-(4-amidinophenyl)ethyl]-3-methyl-6-(2-methoxycarbonyl-2,3-dihydroindol-1-yl-carbonyl)imidazo[4,5-b]pyridine hydrochloride
Yield 20.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCN(C(=O)c1ccc2c(n1)nc(COc1ccc(C(=N)N)cc1)n2C)c1ccccn1
Reaction #78482
1-Methyl-2-[(4-amidinophenyl)oxymethyl]imidazo[4,5-b]pyridin-5-yl-carboxylic acid-N-(2-pyridyl)-N-(2-ethoxycarbonylethyl)amide
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCN(C(=O)c1ccc2sc(CNc3ccc(C(=N)N)cc3)nc2c1)c1ccccc1
Reaction #78488
2-[N-(4-amidinophenyl)aminomethyl]benzothiazole-5-carboxylic acid-N-phenyl-N-(2-ethoxycarbonylethyl)amide
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCN(C(=O)c1ccc2sc(CNc3ccc(C(=N)N)cc3)nc2c1)c1ccccn1.Cl.Cl
Reaction #78490
2-[N-(4-amidinophenyl)aminomethyl]benzothiazol-5-yl-carboxylic acid-N-(2-pyridyl)-N-(2-methoxycarbonylethyl)amide dihydrochloride
Yield 68.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CN(C(=O)c1ccc2sc(CCc3ccc(C(=N)N)cc3)nc2c1)c1ccccn1.Cl.Cl
Reaction #78491
2-[2-(4-amidinophenyl)ethyl]benzothiazol-5-yl-carboxylic acid-N-(2-pyridyl)-N-(ethoxycarbonylmethyl)amide dihydrochloride
Yield 95.0%DOI: 10.6084/m9.figshare.5104873.v1
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