Substructure Search

773711

Cc1n(CC(=O)NCCSSCCNC(=O)Cn2c(C)[n+](C)c3ccccc32)c2ccccc2[n+]1C.[Cl-].[Cl-]
Reaction #40264
white powder
Yield 129.8%DOI: 10.6084/m9.figshare.5104873.v1
C[n+]1c(C=Cc2ccc(N(CCO)CCO)cc2)n(CC(=O)NCCSSCCNC(=O)Cn2c(C=Cc3ccc(N(CCO)CCO)cc3)[n+](C)c3ccccc32)c2ccccc21.[Cl-].[Cl-]
Reaction #40265
orange solid
Yield 163.3%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)C(=O)OCC(C)O
Reaction #48472
HPMA
DOI: 10.6084/m9.figshare.5104873.v1
CCCCC/C=C\C/C=C\C/C=C\C/C=C\CCCC(=O)NCCSSCCNC(=O)CCC/C=C\C/C=C\C/C=C\C/C=C\CCCCC
Reaction #75531
N,N′-diarachidonoylcystamine
Yield 75.0%DOI: 10.6084/m9.figshare.5104873.v1
NCCSSCCN.O=C(O)c1ccccc1-c1c2ccc(=O)cc-2oc2cc(O)ccc12
Reaction #92032
fluorescein cystamine
DOI: 10.6084/m9.figshare.5104873.v1
[N-]=[N+]=Nc1ccc(S(=O)(=O)NCCSSCCNC(=O)CCC(=O)O)cc1
Reaction #351976
N-(p-azidobenzenesulfonyl) N'-(3-carboxypropionyl) cystamine
DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2cccc3c(Cl)ccc(c23)C(=O)N1CCSSCCN1C(=O)c2cccc3c(Cl)ccc(c23)C1=O
Reaction #507595
2,2′-(disulfanediyldiethane-2,1-diyl)bis(6-chloro-1H-benzo[de]-isoquinoline-1,3(2H)-dione)
DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCCSSCCNC(=O)c1ccc(OC(F)(F)F)cc1)c1ccc(OC(F)(F)F)cc1
Reaction #523831
N,N'-(Dithiodiethylene)bis(4-trifluoromethoxybenzamide)
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc[n+](CC(=O)NCCSSCCNC(=O)C[n+]2ccc(C)cc2)cc1.[Cl-].[Cl-]
Reaction #742268
1,1′-{disulphanediylbis[ethane-2,1-diylimino(2-oxoethane-2,1-diyl)]}bis(4-methylpyridinium)dichloride
DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccc(NCCSSCCNc2ccc([N+](=O)[O-])cc2[N+](=O)[O-])c([N+](=O)[O-])c1
Reaction #791727
N,N'-bis (2,4-dinitrophenyl)cystamine
DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2cccc3c(Cl)ccc(c23)C(=O)N1CCSSCCN1C(=O)c2cccc3c(Cl)ccc(c23)C1=O
Reaction #1130533
2,2′-(Disulphanediyldiethane-2,1-diyl)bis(6-chloro-1H-benzo[de]-isoquinoline-1,3(2H)-dione)
DOI: 10.6084/m9.figshare.5104873.v1
CN(C)CCCNc1ccc2c3c(cccc13)C(=O)N(CCSSCCN1C(=O)c3cccc4c(NCCCN(C)C)ccc(c34)C1=O)C2=O
Reaction #1130534
2,2′-(Disulphanediyldiethane-2,1-diyl)bis[6-{[3-(dimethylamino)propyl]-amino}-1H-benzo[de]isoquinoline-1,3(2H)-dione]
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc[n+](CC(=O)NCCSSCCNC(=O)C[n+]2ccc(C)cc2)cc1.[Cl-].[Cl-]
Reaction #1130536
1,1′-{disulphanediylbis[ethane-2,1-diylimino(2-oxoethane-2,1-diyl)]}bis(4-methylpyridinium)dichloride
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CC(N(C)C)C1(c2ccc(Cl)cc2)CCC1.CC[C@H](C)[C@H](NC(=O)[C@H](C)NC(=O)CNC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CO)NC(=O)[C@H](CO)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@@H](NC(=O)[C@H](C)NC(=O)[C@@H]1CSSC[C@H](NC(=O)[C@@H](N)CCCCN)C(=O)N[C@H](CC(N)=O)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](C)C(=O)N[C@@H]([C@@H](C)O)C(=O)N1)[C@@H](C)O)C(C)C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CO)C(=O)N[C@@H](CO)C(=O)N[C@H](C(=O)N[C@@H](CC(N)=O)C(=O)N[C@H](C(=O)NCC(=O)N[C@@H](CO)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)O)[C@@H](C)O)C(C)C)[C@@H](C)O
Reaction #1447092
Amylin Sibutramine
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)[C@@H]1CSSC[C@H](NC(=O)[C@@H]2[C@@H](c3ccc(O)cc3)CCN2C(=O)C(C)(C)C)C(=O)NCCC2(CCCC2)C(=O)N1
Reaction #1474101
(8R,13R)-13-[[[1-(2,2-dimethyl-1-oxopropyl)-3-(R)-(4-hydroxyphenyl)-2-(S)-pyrrolidinyl]carbonyl]amino]-6,14-dioxo-10,11-dithia-7,15-diazaspiro[4.12]heptadecane-8-carboxylic acid 1,1-dimethylethyl ester
Yield 94.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)[C@@H]1CSSC[C@H](NC(=O)[C@H]2NCC[C@@H]2c2ccc(O)cc2)C(=O)NCCC2(CCCC2)C(=O)N1
Reaction #1474102
(8R,13R)-13-[[[3(R)-(4-hydroxyphenyl)-2(S)-pyrrolidinyl]carbonyl]amino]-6,14-dioxo-10,11-dithia-7,15-diazaspiro[4.12]heptadecane-8-carboxylic acid 1,1-dimethylethyl ester
Yield 115.4%DOI: 10.6084/m9.figshare.5104873.v1
N[C@@H](CSSC[C@H](N)C(=O)O)C(=O)O
Reaction #1476767
L-cystine
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCC(=O)N[C@@H](CSSC[C@H](NC(=O)CCCCC)C(=O)OC)C(=O)OC
Reaction #1507306
(R,R)-N,N'-dihexanoyl-3,3'-dithiobis(2-aminopropionic acid) dimethylester
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(CO)[C@@H](O)C(=O)NCCC(=O)NCCSSCCNC(=O)CCNC(=O)[C@H](O)C(C)(C)CO
Reaction #1526808
pantethine
Yield 69.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(CO)[C@@H](O)C(=O)NCCC(=O)NCCSSCCNC(=O)CCNC(=O)[C@H](O)C(C)(C)CO
Reaction #1526809
pantethine
Yield 69.2%DOI: 10.6084/m9.figshare.5104873.v1
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