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235021

C=Cc1cc(-c2ccc(O)cc2)nc2ccc(O)cc12
Reaction #7336
2-(4-Hydroxyphenyl)-4-vinylquinolin-6-ol
Выход 69.0%DOI: 10.6084/m9.figshare.5104873.v1
C=Cc1cc(-c2ccc(O)c(F)c2)nc2c(Cl)cc(O)cc12
Reaction #7353
8-Chloro-2-(3-fluoro-4-hydroxyphenyl)-4-vinylquinolin-6-ol
Выход 84.0%DOI: 10.6084/m9.figshare.5104873.v1
NCCCc1ccnc2ccccc12
Reaction #11542
titled compound
Выход 76.3%DOI: 10.6084/m9.figshare.5104873.v1
NCCCc1ccnc2ccccc12
Reaction #46667
compound
Выход 76.3%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)/C=C/c1cc(=O)n(CC=O)c2cc(OC)ccc12
Reaction #68039
ethyl (2E)-3-(7-methoxy-2-oxo-1-(2-oxoethyl)-1,2-dihydroquinolin-4-yl)acrylate
Выход 59.8%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)/C=C/c1cc(=O)n(CCN2CCC(N(Cc3ccc4c(c3)OCCO4)C(=O)OC(C)(C)C)CC2)c2cc(OC)ccc12
Reaction #68040
ethyl (2E)-3-(1-(2-(4-((tert-butoxycarbonyl)(2,3-dihydro-1,4-benzodioxin-6-ylmethyl)amino)piperidin-1-yl)ethyl)-7-methoxy-2-oxo-1,2-dihydroquinolin-4-yl)acrylate
Выход 63.7%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)/C=C/c1cc(=O)n(CCN2CCC(NCc3ccc4c(c3)OCCO4)CC2)c2cc(OC)ccc12
Reaction #68041
ethyl (2E)-3-(1-(2-(4-((2,3-dihydro-1,4-benzodioxin-6-ylmethyl)amino)piperidin-1-yl)ethyl)-7-methoxy-2-oxo-1,2-dihydroquinolin-4-yl)acrylate
Выход 80.4%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(/C=C/C(=O)O)cc(=O)n(CCN3CCC(NCc4ccc5c(c4)OCCO5)CC3)c2c1
Reaction #68042
(2E)-3-(1-(2-(4-((2,3-dihydro-1,4-benzodioxin-6-ylmethyl)amino)piperidin-1-yl)ethyl)-7-methoxy-2-oxo-1,2-dihydroquinolin-4-yl)acrylic acid
Выход 77.8%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(/C=C/C(N)=O)cc(=O)n(CC=O)c2c1
Reaction #68121
(2E)-3-(7-methoxy-2-oxo-1-(2-oxoethyl)-1,2-dihydroquinolin-4-yl)acrylamide
Выход 56.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C/C=C/c1ccnc2ccccc12
Reaction #78846
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2nc(Cl)cc(C=CN(C)C)c2c1
Reaction #182120
DOI: 10.1039/C8SC04228D
O=Cc1ccnc2c(NC(=O)c3c(Cl)cccc3Cl)cccc12
Reaction #209895
DOI: 10.1039/C8SC04228D
NC(=O)Nc1ccc2c(c1)C(=Cc1ccnc3ccccc13)C(=O)N2
Reaction #229565
DOI: 10.1039/C8SC04228D
O=C1NC(=S)SC1=Cc1ccnc2ccccc12
Reaction #244149
DOI: 10.1039/C8SC04228D
O=[N+]([O-])c1cccc(C=Cc2ccnc3ccccc23)c1
Reaction #258986
DOI: 10.1039/C8SC04228D
COc1cc(F)c2nccc(C(=O)CBr)c2c1
Reaction #279150
DOI: 10.1039/C8SC04228D
C=C(c1cn(C(c2ccccc2)(c2ccccc2)c2ccccc2)cn1)c1ccnc2ccccc12
Reaction #293575
DOI: 10.1039/C8SC04228D
CCN(CC)c1ccc2cc(/C=C/c3cc[n+](CCCCCC(=O)O)c4ccc(S(=O)(=O)O)cc34)c(=O)oc2c1.C[N+](C)(C)CC(=O)O
Reaction #316961
1-(5-carboxy-pentyl)-4-[(E)-2-(7-diethylamino-2-oxo-2H-chromen-3-yl)-vinyl]-6-sulfo-chinolinium betaine
DOI: 10.6084/m9.figshare.5104873.v1
CCN(CC)c1ccc2cc(/C=C/c3cc[n+](CCCCCC(=O)O)c4ccc(S(=O)(=O)[O-])cc34)oc2c1.C[N+](C)(C)CC(=O)O
Reaction #316962
1-(5-carboxy-pentyl)-4-[(E)-2-(6-diethylamino-benzofuran-2-yl)-vinyl]-6-sulfonato-chinolinium betaine
DOI: 10.6084/m9.figshare.5104873.v1
CCN1C(=CC=CC=Cc2cc[n+](CCCCCC(=O)O)c3ccccc23)C(C)(C)c2cc(P(=O)(O)O)ccc21.[Cl-]
Reaction #339978
compound 15
DOI: 10.6084/m9.figshare.5104873.v1
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