子结构搜索

1226225

N=C(N)NC(SSC[C@H](N)C(=O)O)[C@H](N)C(=O)O
Reaction #8486
Guanidino-L-cystine
DOI: 10.6084/m9.figshare.5104873.v1
Cc1n(C)c2ccccc2[n+]1CCSSCC[n+]1c(C)n(C)c2ccccc21.[Br-].[Br-]
Reaction #40263
3,3′-(disulfanediyldiethane-2,1-diyl)bis(1,2-dimethyl-1H-benzimidazol-3-ium) dibromide
DOI: 10.6084/m9.figshare.5104873.v1
Cc1n(CC(=O)NCCSSCCNC(=O)Cn2c(C)[n+](C)c3ccccc32)c2ccccc2[n+]1C.[Cl-].[Cl-]
Reaction #40264
white powder
收率 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
收率 163.3%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)[O-].CS(=O)(=O)[O-].c1c[n+](CCSSCC[n+]2ccc3c(c2)CCCC3)cc2c1CCCC2
Reaction #47787
2,2′-(disulfanediyldiethane-2,1-diyl)bis(5,6,7,8-tetrahydroisoquinolinium) dimethane sulfonate
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
收率 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
CCCCCCCCCC=O.C[C@@H](O)[C@@H]1NC(=O)[C@H](CCCCN)NC(=O)[C@@H](Cc2c[nH]c3ccccc23)NC(=O)[C@H](Cc2ccccc2)NC(=O)[C@@H](NC(=O)[C@H](N)Cc2ccccc2)CSSC[C@@H](C(=O)N[C@H](CO)[C@@H](C)O)NC1=O
Reaction #164434
Decanal Octreotide
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NCCSSCCNC(=O)c1ccccc1O
Reaction #172582
tert-butyl 2-(2-(2-(2-hydroxybenzamido)ethyl)disulfanyl)ethylcarbamate
收率 54.2%DOI: 10.6084/m9.figshare.5104873.v1
NCCSSCCNC(=O)c1ccccc1O
Reaction #172583
N-(2-(2-(2-aminoethyl)-disulfanyl)-ethyl)-2-hydroxybenzamide
DOI: 10.6084/m9.figshare.5104873.v1
CC/C=C\C/C=C\C/C=C\C/C=C\C/C=C\C/C=C\CCC(=O)NCCSSCCNC(=O)c1ccccc1O
Reaction #172584
N-(2-(2-(2-(4Z,7Z,10Z,13Z,16Z,19Z)-docosa-4,7,10,13,16,19-hexaenamidoethyl)disulfanyl)ethyl)-2-hydroxybenzamide
收率 44.5%DOI: 10.6084/m9.figshare.5104873.v1
[N-]=[N+]=Nc1ccc(S(=O)(=O)NCCSSCCNC(=O)CCC(=O)O)cc1
Reaction #269085
DOI: 10.1039/C8SC04228D
NCCSSCCNC(=O)c1cccnc1
Reaction #278893
DOI: 10.1039/C8SC04228D
CCCCCCCCCC=O.C[C@@H](O)[C@@H]1NC(=O)[C@H](CCCCN)NC(=O)[C@@H](Cc2c[nH]c3ccccc23)NC(=O)[C@H](Cc2ccccc2)NC(=O)[C@@H](NC(=O)[C@H](N)Cc2ccccc2)CSSC[C@@H](C(=O)N[C@H](CO)[C@@H](C)O)NC1=O
Reaction #308366
Decanal Octreotide
DOI: 10.6084/m9.figshare.5104873.v1
O=c1[nH]c(NCCSSCCNc2ncc(Cc3cccnc3)c(=O)[nH]2)ncc1Cc1cccnc1
Reaction #312056
2-[5-(3-pyridylmethyl)-4-oxo-2-pyrimidylamino]ethyl disulphide
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
CC(=O)N[C@@H](CSSC[C@H](NC(C)=O)C(=O)[O-])C(=O)[O-].[NH3+]CC[NH3+]
Reaction #353587
title compound
收率 52.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N[C@@H](CSSC[C@H](NC(C)=O)C(=O)[O-])C(=O)[O-].c1ccc(C[NH2+]CC[NH2+]Cc2ccccc2)cc1
Reaction #353588
N,N'-dibenzylethylenediarniniurn N,N'-diacetyl-L-cystinate
DOI: 10.6084/m9.figshare.5104873.v1
C1C[NH2+]CCN1.CC(=O)N[C@@H](CSSC[C@H](NC(C)=O)C(=O)[O-])C(=O)[O-]
Reaction #353589
Piperazinium N,N'-diacetyl-L-cystinate
DOI: 10.6084/m9.figshare.5104873.v1
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