764019
Dibenzocyclooctyne-PEG4-N-hydroxysuccinimidyl ester
≥90%
Sinônimo(s):
DBCO-PEG4-NHS ester, DBCO-PEG4-SE, DBCO-PEG4-succinimidyl ester
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About This Item
Fórmula empírica (Notação de Hill):
C34H39N3O10
Peso molecular:
649.69
Número MDL:
Código UNSPSC:
12352108
ID de substância PubChem:
NACRES:
NA.22
Produtos recomendados
Nível de qualidade
Ensaio
≥90%
Formulário
paste
adequação da reação
reaction type: click chemistry
reagent type: linker
grupo funcional
NHS ester
temperatura de armazenamento
−20°C
cadeia de caracteres SMILES
O=C(CCC(NCCOCCOCCOCCOCCC(ON1C(CCC1=O)=O)=O)=O)N2CC3=C(C=CC=C3)C#CC4=C2C=CC=C4
InChI
1S/C34H39N3O10/c38-30(11-12-31(39)36-25-28-7-2-1-5-26(28)9-10-27-6-3-4-8-29(27)36)35-16-18-44-20-22-46-24-23-45-21-19-43-17-15-34(42)47-37-32(40)13-14-33(37)41/h1-8H,11-25H2,(H,35,38)
chave InChI
RRCXYKNJTKJNTD-UHFFFAOYSA-N
Categorias relacionadas
Aplicação
Dibenzocyclooctyne-PEG4-N-hydroxysuccinimidyl ester may be used in the synthesis of a prostate-specific membrane antigen (PSMA)-targeted single photon emission computed tomography (SPECT) agent via copper-less click chemistry.
Succinimidyl ester (NHS, amine reactive) functionalized cyclooctyne derivative for incorporation of the cyclooctyne moiety into amine containing compounds or biomolecules. Cyclooctynes are useful in strain-promoted copper-free click chemistry cycloaddition reactions. This dibenzocyclooctyne will react with azide functionalized compounds or biomolecules without the need for a Cu(I) catalyst to result in a stable triazole linkage.
Applications Include:
Applications Include:
- Protein-peptide conjugates
- Antibody-enzyme or antibody-drug conjugates
- Protein or peptide-oligonucleotide conjugates
- Surface modification
Código de classe de armazenamento
11 - Combustible Solids
Classe de risco de água (WGK)
WGK 3
Ponto de fulgor (°F)
Not applicable
Ponto de fulgor (°C)
Not applicable
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Global Trade Item Number
| SKU | GTIN |
|---|---|
| 764019-5MG | 4061833230862 |
| 764019-1MG | 4061826701638 |
| 764019-50MG | 4061832922980 |
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