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CCC[C@H](N)C(=O)NC1CCN(c2ccn3c(=O)c(C(=O)O)ccc3c2)C1
Reaction #1942
amino acid
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #1946
amino acid
DOI: 10.6084/m9.figshare.5104873.v1
Cl.NCCNC(=O)c1cc(-c2ccnc(Nc3cccc(Cl)c3)n2)ccn1
Reaction #2256
N-[3-chloro-phenyl]-4-[2-(N-{2-amino-ethyl}-aminocarbonyl)-4-pyridyl]-2-pyrimidineamine hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CNC(=O)CCCn1cnc2c1N=CNCC2O
Reaction #3076
N-(4-(3,6,7,8-tetrahydro-imidazo[4,5-d]-[1,3]diazepin-8-ol-3-yl)butyryl)glycine ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(C(=O)ON2C(=O)CCC2=O)cc1
Reaction #3765
4-toluic acid succinimidyl ester
Ausbeute 94.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)ON1C(=O)CCC1=O
Reaction #3766
acetic acid succinimidyl ester
Ausbeute 70.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(C(=O)ON2C(=O)CCC2=O)cc1
Reaction #3767
4-toluic acid succinimidyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCC(=O)N[C@@H](C)C(=O)N[C@H](CCC(=O)ON1C(=O)CCC1=O)C(=O)OCc1ccccc1
Reaction #4519
palmitoyl-L-Ala-D-Glu(OSu)OBzl
Ausbeute 7846.1%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCC(=O)N[C@@H](C)C(=O)N[C@H](CCC(=O)ON1C(=O)CCC1=O)C(=O)OCc1ccccc1
Reaction #4520
palmitoyl-L-Ala-D-Glu(OH)OBzl
DOI: 10.6084/m9.figshare.5104873.v1
N#CNC(=O)CNC(=O)c1ccccc1
Reaction #4590
N-Benzoylglycylcyanamide
Ausbeute 56.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C[C@H](NC(=O)c1ccccc1)C(=O)NC#N
Reaction #4592
N-Benzoyl-L-leucylcyanamide
Ausbeute 42.9%DOI: 10.6084/m9.figshare.5104873.v1
N#CNC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H]1CCC(=O)N1
Reaction #4594
15
Ausbeute 42.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C(ON1C(=O)CCC1=O)c1cccnc1
Reaction #4674
N-Nicotinoyloxysuccinimide
Ausbeute 72.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N[C@@H](C)C(=O)N[C@@H](CCCCNC(=O)OC(C)(C)C)C(=O)O
Reaction #5077
Ac-Ala-Lys(Boc)-OH
DOI: 10.6084/m9.figshare.5104873.v1
NCCCNC(=O)OCc1ccccc1
Reaction #5651
title compound
Ausbeute 80.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1cc(C(=O)NCCCSc2ccncc2)cc(C(C)(C)C)c1O
Reaction #6207
desired compound
Ausbeute 27.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCCCSc1ccncc1)c1ccsc1
Reaction #6217
desired compound
Ausbeute 76.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cc1cccs1)NCCCSc1ccncc1
Reaction #6218
desired compound
Ausbeute 86.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCCCSc1ccncc1)c1cc(Br)c(Br)s1
Reaction #6219
desired compound
Ausbeute 71.8%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(C(=O)NCCCSc2ccncc2)s1
Reaction #6220
desired compound
Ausbeute 64.5%DOI: 10.6084/m9.figshare.5104873.v1
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