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CC[C@H](C)[C@@H]([C@@H](CC(=O)N1CCC[C@H]1[C@H](OC)[C@@H](C)C(=O)N[C@@H](Cc1ccccc1)C(=O)O)OC)N(C)C(=O)[C@@H](NC(=O)C(C)(C)N(C)C(=O)CCCN1C(=O)C=CC1=O)C(C)C
Reaction #162009
N-[4-(2,5-dioxo-2,5-dihydro-1H-pyrrol-1-yl)butanoyl]-N,2-dimethylalanyl-N-{(1S,2R)-4-{(2S)-2-[(1R,2R)-3-{[(1S)-1-carboxy-2-phenylethyl]amino}-1-methoxy-2-methyl-3-oxopropyl]pyrrolidin-1-yl}-2-methoxy-1-[(1S)-1-methylpropyl]-4-oxobutyl}-N-methyl-L-valinamide
DOI: 10.6084/m9.figshare.5104873.v1
NNC(=S)NN(Cc1ccccc1)C(=O)CCCN1C(=O)C=CC1=O.O=C(O)CN(CCN(CC(=O)O)CC(=O)O)CC(=O)O
Reaction #320007
EDTA benzyl(gamma-maleimidobutyryl)thiocarbazide
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)c1cc(-c2nnc(O)n2-c2ccc3c(ccn3CCN(C)C(=O)CCCN3C(=O)C=CC3=O)c2)c(O)cc1O
Reaction #512084
N-(2-(5-(3-(2,4-dihydroxy-5-isopropylphenyl)-5-hydroxy-4H-1,2,4-triazol-4-yl)-1H-indol-1-yl)ethyl)-4-(2,5-dioxo-2,5-dihydro-1H-pyrrol-1-yl)-N-methylbutanamide
Выход 46.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)c1cc(-c2nnc(O)n2-c2ccc3c(ccn3CCN(C)C(=O)CCCN3C(=O)C=CC3=O)c2)c(O)cc1O
Reaction #536995
N-(2-(5-(3-(2,4-dihydroxy-5-isopropylphenyl)-5-hydroxy-4H-1,2,4-triazol-4-yl)-1H-indol-1-yl)ethyl)-4-(2,5-dioxo-2,5-dihydro-1H-pyrrol-1-yl)-N-methylbutanamide
Выход 46.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(CCN1C(=O)C=CC1=O)C(=O)O
Reaction #969763
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CC(CN1C(=O)C=CC1=O)S(=O)(=O)O
Reaction #969853
title product
Выход 75.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(CC(CN1C(=O)C=CC1=O)S(=O)(=O)O)ON1C(=O)CCC1=O
Reaction #969854
title product
Выход 75.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)CCNC(=O)CNC(=O)CNC(=O)CN.NCCCC(=O)O
Reaction #969860
title compound
Выход 78.4%DOI: 10.6084/m9.figshare.5104873.v1
O=C(CC(CN1C(=O)C=CC1=O)S(=O)(=O)O)ON1C(=O)CCC1=O
Reaction #1031298
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)NNC(=O)CCCN1C(=O)C=CC1=O
Reaction #1229166
DOI: 10.1039/C8SC04228D
O=C(O)CCCN1C(=O)C=CC1=O
Reaction #1317963
DOI: 10.1039/C8SC04228D
O=C(O)CCCN1C(=O)C=CC1=O
Reaction #1334184
title compound
Выход 48.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)c1cc(-c2nnc(O)n2-c2ccc3c(ccn3CCN(C)C(=O)CCCN3C(=O)C=CC3=O)c2)c(O)cc1O
Reaction #1515817
N-(2-(5-(3-(2,4-dihydroxy-5-isopropylphenyl)-5-hydroxy-4H-1,2,4-triazol-4-yl)-1H-indol-1-yl)ethyl)-4-(2,5-dioxo-2,5-dihydro-1H-pyrrol-1-yl)-N-methylbutanamide
Выход 46.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CC(CN1C(=O)C=CC1=O)S(=O)(=O)O
Reaction #1652151
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)NNC(=O)CCCN1C(=O)C=CC1=O
Reaction #1863868
title compound
Выход 85.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCn1nc2c(N)nc3ccccc3c2c1CC1CCN(C(=O)CCCN2C(=O)C=CC2=O)CC1
Reaction #1932900
1-(4-{4-[(4-amino-2-propyl-2H-pyrazolo[3,4-c]quinolin-1-yl)methyl]piperidin-1-yl}-4-oxobutyl)-1H-pyrrole-2,5-dione
Выход 37.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CC(CN1C(=O)C=CC1=O)S(=O)(=O)O
Reaction #2001627
title product
Выход 75.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(CC(CN1C(=O)C=CC1=O)S(=O)(=O)O)ON1C(=O)CCC1=O
Reaction #2001628
title product
Выход 75.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)CCNC(=O)CNC(=O)CNC(=O)CN.NCCCC(=O)O
Reaction #2001634
title compound
Выход 78.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NNC(=O)CCCN1C(=O)C=CC1=O
Reaction #2055685
title compound
Выход 85.0%DOI: 10.6084/m9.figshare.5104873.v1
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