Teilstruktursuche

CSCCNC(=O)CSC

CSCCN1CSC(=Cc2cc(C(C)(C)C)c(O)c(C(C)(C)C)c2)C1=O
Reaction #3033
title compound
DOI: 10.6084/m9.figshare.5104873.v1
NCC(O)C[n+]1ccc(SCC2=C(C(=O)O)N3C(=O)[C@@H](NC(=O)CSc4cc(Cl)ccc4Cl)[C@H]3SC2)cc1.[Cl-]
Reaction #3762
title compound
Ausbeute 127.2%DOI: 10.6084/m9.figshare.5104873.v1
CCCC(=O)N1CCN(C(=O)OC2C3=C(SCCS3)C(=O)N2c2ccc3ccc(Cl)nc3n2)CC1
Reaction #55361
5-(4-Butyrylpiperazin-1-yl)carbonyloxy-6-(7-chloro-1,8-naphthyridin-2-yl)-7-oxo-2,3,6,7-tetrahydro-5H-1,4-dithiino[2,3-c]pyrrole
Ausbeute 67.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N1CCN(C(=O)OC2C3=C(SCCS3)C(=O)N2c2ccc3ccc(Cl)nc3n2)CC1
Reaction #55363
5-(4-Acetylpiperazin-1-yl)carbonyloxy-6-(7-chloro-1,8-naphthyridin-2-yl)-7-oxo-2,3,6,7-tetrahydro-5H-1,4-dithiino[2,3-c]pyrrole
Ausbeute 38.9%DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)CCC(Sc1nnn[nH]1)C1=C(C(=O)O)N2C(=O)C(NC(=O)CSC(F)(F)F)[C@H]2SC1
Reaction #55411
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CSCC(=O)NC1C(=O)N2C(C(=O)O)=C(C(CCC(N)=O)Sc3nnn[nH]3)CS[C@H]12
Reaction #55414
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1SC(=O)C2CSCN2C1=O
Reaction #63634
6-methyl-1H,3H-thiazolo[4,3-c][1,4]thiazine-5,8-dione
Ausbeute 50.8%DOI: 10.6084/m9.figshare.5104873.v1
CSCCNCCSC
Reaction #184499
DOI: 10.1039/C8SC04228D
O=C(C[n+]1ccc(CN2CCC(=CC3=C(C(=O)[O-])N4C(=O)C(NC(=O)CSc5cc(Cl)c(Cl)cc5Cl)C4SC3)C2=O)cc1)Nc1ccc(O)c(F)c1
Reaction #188091
DOI: 10.1039/C8SC04228D
Cc1cc(SCC(=O)NC2C(=O)N3C(C(=O)O)=C(C=C4CCN(Cc5ccc(O)cc5)C4=O)CSC23)n2nc(-c3ccc(O)c(O)c3)nc2n1
Reaction #190929
DOI: 10.1039/C8SC04228D
CSCCN1CSC(=Cc2cc(C(C)(C)C)c(O)c(C(C)(C)C)c2)C1=O
Reaction #191541
DOI: 10.1039/C8SC04228D
CC1(C)SC2C(NC(=O)CSc3ccncc3)C(=O)N2C1c1nnn[nH]1
Reaction #192053
DOI: 10.1039/C8SC04228D
CC(C)(C)C(=O)SC[C@H](NC(=O)C(C)(C)SC(=O)C(C)(C)C)C(=O)O
Reaction #214475
S-pivaloyl-N-(S-pivaloyl-2-mercapto-2-methylpropanoyl)-L-cysteine
Ausbeute 16.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(SCC(=O)O)C(=O)N[C@@H](CSCC(=O)O)C(=O)O
Reaction #214477
S-carboxymethyl-N-(2-carboxymethylthio-2-methylpropanoyl)-L-cysteine
Ausbeute 194.5%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc(CN2CCC(=CC3=C(C(=O)O)N4C(=O)C(NC(=O)CSc5ccccc5)C4SC3)C2=O)cc1
Reaction #237131
DOI: 10.1039/C8SC04228D
Cc1ccc(C(=O)SC(C)C(=O)N2CSCC2C(=O)O)cc1
Reaction #246086
DOI: 10.1039/C8SC04228D
COc1ccc(N2C(=O)C3=C(SCCS3)C2CC(=O)N2CCCCC2)cc1
Reaction #252516
DOI: 10.1039/C8SC04228D
O=C(CCSCC(=O)N1CCSCC1)OCc1ccccc1
Reaction #256517
DOI: 10.1039/C8SC04228D
O=C(C[n+]1ccc(CN2CCC(=CC3=C(C(=O)[O-])N4C(=O)C(NC(=O)CSc5ccncc5)C4SC3)C2=O)cc1)Nc1ccc(O)cc1
Reaction #258089
DOI: 10.1039/C8SC04228D
O=C(C[n+]1ccc(CN2CCC(=CC3=C(C(=O)[O-])N4C(=O)C(NC(=O)CSc5ccc(O)cc5)C4SC3)C2=O)cc1)Nc1ccc(O)c(F)c1
Reaction #259275
DOI: 10.1039/C8SC04228D
Seite 1Weiter