Alkyne-PEG(4)-Val-Ala-PAB-Cl

Nom chimique: Propargyl-tetraethyleneglycol-propanoyl-valyl-alanyl-(4-aminobenzyl chloride) // Synonymes: (S)-N-((S)-1-((4-(Chloromethyl)phenyl)amino)-1-oxopropan-2-yl)-3-methyl-2-(3-(2-(prop-2-yn-1-yloxy)ethoxy)propanamido)butanamide, Propargyl-PEG(4)-Val-Ala-PAB-Cl,Alkyne-PEG(4)-VA-PAB-Cl

  • n° Art.:ADC1720
  • Formule:C29H44ClN3O8
  • Storage temperature:-20°C
  • Masse moléculaire:598,13 g/mol

from 500,00 €

Grouped product items
Nombre Unité de vente Prix SKU Disponibilité
100 mg
500,00 €
ADC1720.0100
sur demande
250 mg
1 000,00 €
ADC1720.0250
sur demande
description

Linker for Antibody-Drug-Conjugation (ADC). In contrast to the hydroxybenzyl derivative ADC1350 the chloride is able to react with tertiary amines to form a linked quarternary amine. The Val-Ala will specifically be cleaved by Cathepsin B. As this enzyme is only present in the lysosome the ADC payload will be released only in the cell. The alkyne moiety allows versatile conjugation e.g. via Click Chemistry.


references

Laurent Ducry (ed.), Antibody-Drug Conjugates, Methods in Molecular Biology, vol. 1045, Springer Science+Business Media, LLC 2013; https://doi.org/10.1007/978-1-62703-541-5_5.


Development of Novel Quaternary Ammonium Linkers for Antibody-Drug Conjugates; P. J. Burke, J. Z. Hamilton, T. A. Pires, J. R. Setter. J. H. Hunter, J. H. Cochran, A. B. Waight, K. A. Gordon, B. E. Toki, K. K. Emmerton, W. Zeng, I. J. Stone, P. D. Senter, R. P. Lyon, S. C. Jeffrey; Mol. Cancer Ther. 2016; 15(5): 938-954. https://doi.org/10.1158/1535-7163.MCT-16-0038.

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