Development of the Traceless Phenylhydrazide Linker for

Development of the Traceless Phenylhydrazide Linker for The hydrazide group is an oxidatively cleavable traceless linker for solid-phase chemistry. This linker technology was used to develop a multistep solid-phase synthesis of an antibiotic that is Releasable conjugation of polymers to proteins 1 Releasable conjugation of polymers to proteins Yuhui Gong1, Jean-Christophe Leroux1, and Marc A. Gauthier2,* 1 Swiss Federal Institute of Technology Zurich (ETHZ), Department of Chemistry and Applied Biosciences, Institute of Pharmaceutical Sciences, Vladimir-Prelog-Weg 1–5/10, 8093 Zurich, Linkers for Antibody Drug Conjugates: Current Role and

The use of self-immolative linkers has permitted temporary drug conjugation to polymers and antibodies. In the case of antibody–drug conjugates, these linkers can be engineered to act as ‘traceless’ bond from which cleavage results in the native antibody and unmodified drug . Self-immolative linkers containing disulfides have hypothesized

These linkers show non-specific function after cleavage. Traceless linkers are so called because an examination of the final compound reveals no trace of the point of linkage to the solid phase. The oldest definition for „traceless“ traces back to the import of a Hydrogenatom instead of the previous linker.

Traceless and multifunctional linkers for the generation

Site-specific chemical modification of antibody fragments using traceless cleavable linkers. Gonçalo J L Bernardes 1,2,3, Martina Steiner 1, Isabelle Hartmann 1, Dario Neri 1 & Delivery and Release of Small-Molecule Probes in Here, we describe cleavable linkers designed for the traceless release of chemical cargo from MPPs following mitochondrial transit. The cleavage kinetics of a number of disulfides were investigated using a fluorescent reporter system in order to optimize linker stability for mitochondrial release. The stability of mono- and disubstituted Cleavable vs. Non-Cleavable Linkers in Antibody-Drug Dec 19, 2019 Cleavable linkers in chemical biology - ScienceDirect