Functional sequences of precision polymers based on thiolactone/Michael chemistry are identified from a large one-bead one-compound library. Single-bead readout by MALDI-TOF MS/MS identifies sequences that host m-THPC that is a second generation photo-sensitizer drug. The corresponding Tla/Michael-PEG conjugates make m-THPC available in solution and drug payload as well as drug release kinetics can be fine-tuned by the precision segment
Chemical cross-linkers have proven valuable for a diversity of biological applications such as prote...
A sequential thiol-Michael - radical thiol-ene (STMRT) strategy was used to produce poly(ethylene gl...
A practical synthesis of unique, precisely decorated, multisegmented block copolymers was elaborated...
A straightforward access route to multifunctional block copolymers, com- bining a poly(ethylene glyc...
Functional sequences of monodisperse, sequence‐defined oligo(amide‐urethane)s are designed based on ...
Designing artificial macromolecules with absolute sequence order represents a considerable challenge...
International audienceAdvanced drug delivery systems (DDS) are easily designed following a photoiter...
AbstractOne-pot multi-step reactions based on thiolactone chemistry emerged as a powerful tool to pr...
Polymer-block-peptide conjugates are tailored to render hydrophobic small molecule drugs water solub...
A straightforward synthetic procedure for the double modification and polymer-polymer conjugation of...
A conceptual proof for the double modification (aminolysis and subsequent thiol-click modification) ...
Molecular recognition binding sites that specifically identify a target molecule are essential for r...
Unique chemical methodology enables the synthesis of innovative and diverse scaffolds and chemotypes...
Unique chemical methodology enables the synthesis of innovative and diverse scaffolds and chemotypes...
Combining poly(ethylene glycol) (PEG) with sequence-defined peptides in PEG–peptide conjugates offe...
Chemical cross-linkers have proven valuable for a diversity of biological applications such as prote...
A sequential thiol-Michael - radical thiol-ene (STMRT) strategy was used to produce poly(ethylene gl...
A practical synthesis of unique, precisely decorated, multisegmented block copolymers was elaborated...
A straightforward access route to multifunctional block copolymers, com- bining a poly(ethylene glyc...
Functional sequences of monodisperse, sequence‐defined oligo(amide‐urethane)s are designed based on ...
Designing artificial macromolecules with absolute sequence order represents a considerable challenge...
International audienceAdvanced drug delivery systems (DDS) are easily designed following a photoiter...
AbstractOne-pot multi-step reactions based on thiolactone chemistry emerged as a powerful tool to pr...
Polymer-block-peptide conjugates are tailored to render hydrophobic small molecule drugs water solub...
A straightforward synthetic procedure for the double modification and polymer-polymer conjugation of...
A conceptual proof for the double modification (aminolysis and subsequent thiol-click modification) ...
Molecular recognition binding sites that specifically identify a target molecule are essential for r...
Unique chemical methodology enables the synthesis of innovative and diverse scaffolds and chemotypes...
Unique chemical methodology enables the synthesis of innovative and diverse scaffolds and chemotypes...
Combining poly(ethylene glycol) (PEG) with sequence-defined peptides in PEG–peptide conjugates offe...
Chemical cross-linkers have proven valuable for a diversity of biological applications such as prote...
A sequential thiol-Michael - radical thiol-ene (STMRT) strategy was used to produce poly(ethylene gl...
A practical synthesis of unique, precisely decorated, multisegmented block copolymers was elaborated...