بحث البنية الفرعية

CC(=O)O.N=CN

CCOC(=O)CN1C(=O)CN(CC(=O)OC)C1=NN=Cc1ccccc1
Reaction #49686
2-benzylidenehydrazono-3-ethoxycarbonylmethyl-1-methoxycarbonylmethylimidazolidin-4-one
المردود 44.4%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CN1C(=O)CN2CC(=O)NN=C21
Reaction #49687
7-ethoxycarbonylmethyl-1,4,5,7-tetraazabicyclo[4,3,0]-nonan-5-ene-3,8-dione
المردود 39.1%DOI: 10.6084/m9.figshare.5104873.v1
CC1=C(C(=O)NCCC(c2ccccc2)c2ccccc2)C(c2cccc(Cl)c2)N=C(N)N1
Reaction #52900
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccnc2c1C(=NNC(=N)N)CC(c1ccccc1Cl)C2.O=C1CC[C@@H](C(=O)O)N1
Reaction #77465
(−)-7-(2-chlorophenyl)-5-guanidinoimino-4-methyl-5,6,7,8-tetrahydroquinoline L-pyroglutamate
المردود 156.8%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccnc2c1C(=NNC(=N)N)CC(c1cc(F)ccc1Cl)C2.O=C1CC[C@@H](C(=O)O)N1
Reaction #77478
(+)-7-(2-chloro-5-fluorophenyl)-5-guanidinoimino-4-methyl-5,6,7,8-tetrahydroquinoline L-pyroglutamate
المردود 42.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(CC(=O)N(C)CCC[P+](c1ccccc1)(c1ccccc1)c1ccccc1)C(=N)[NH3+].O=C([O-])C(F)(F)F.O=C([O-])C(F)(F)F
Reaction #86610
title compound
المردود 18.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CC(CS)C(=O)N[C@@H](CCCNC(=N)N)C(=O)O
Reaction #94068
Nα -[3-Mercapto-2-(methoxycarbonylmethyl)propanoyl]-L-arginine
DOI: 10.6084/m9.figshare.5104873.v1
N=C(N)NCCC[C@H](NC(=O)C(CS)CC(N)=O)C(=O)O
Reaction #94069
Nα -[3-mercapto-2-(carbamoylmethyl)propanoyl]-L-arginine
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CC(CS)C(=O)N[C@@H](CCCCN)C(=O)O
Reaction #94071
Nα -[3-mercapto-2-(methoxycarbonylmethyl)propanoyl]-L-lysine
DOI: 10.6084/m9.figshare.5104873.v1
NCCCC[C@H](NC(=O)C(CS)CC(N)=O)C(=O)O
Reaction #94072
Nα -[2-(carbamoylmethyl)-3-mercaptopropanoyl]-L-lysine
DOI: 10.6084/m9.figshare.5104873.v1
N#CNC(=NCCNC(=O)c1ccccc1Cl)NC1CCCC(c2csc(NC(=N)N)n2)C1.O=C(O)/C=C\C(=O)O
Reaction #94862
2-guanidino-4-{ 3-[3-cyano-2-(2-(2-chlorobenzoylamino)ethyl)guanidino]cyclohexyl}thiazole hydrogen maleate
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(N=C2SCC3(CCCC3)N2C2CCCC2)c(C)c1
Reaction #176121
DOI: 10.1039/C8SC04228D
NC(N)=Nc1nc(-c2cncc(CO)c2)cs1
Reaction #177493
DOI: 10.1039/C8SC04228D
CCC1=[SH]C(=NC(=O)C2=C(C(=O)O)CCC2)N(Cc2ccc(-c3ccccc3-c3nnn[nH]3)cc2)N1
Reaction #181447
DOI: 10.1039/C8SC04228D
COc1ccc(Cn2ncc3cc(C=C4SC(N5CCCC5C(=O)O)=NC4=O)ccc32)c(C(F)(F)F)c1
Reaction #187106
DOI: 10.1039/C8SC04228D
COC(=O)C1=C(C)N=C(OC)N(C)C1c1ccc(F)cc1
Reaction #187171
DOI: 10.1039/C8SC04228D
CCOC(=O)CCC(NC1=NC(=O)C(=Cc2ccc(N3CCC(NCC(O)c4ccc(O)c(NS(C)(=O)=O)c4)CC3)cc2)S1)C(=O)OCC
Reaction #187789
DOI: 10.1039/C8SC04228D
COC(=O)CC1c2cccc(F)c2N=C(N2CCN(c3cccc(OC)c3)CC2)N1c1cc(C(F)(F)F)ccc1OC
Reaction #188096
DOI: 10.1039/C8SC04228D
CCCCCN(CCCNC(=O)C(NC(=O)C(NC(=O)NC(C(=O)O)C(C)C)C1CCNC(=N)N1)C(O)C(C)C)C(C(=O)O)C(OC1OC(CN)C(O)C1OC)C1OC(n2ccc(=O)[nH]c2=O)C(O)C1O
Reaction #207757
DOI: 10.1039/C8SC04228D
Cc1ccc2[nH]c(NC(Cc3ccc(OCCCC(=O)NC4=NCCCN4)cc3)C(=O)O)nc2c1
Reaction #212918
DOI: 10.1039/C8SC04228D
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