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Profil bibliographique

Martin Wilkovitsch

Informations fournies par OpenAlex. Research Africa ne déduit ni nationalité, ni poste, ni coordonnées personnelles.

39Publications signalées
539Citations signalées
1Affiliations récentes

Les institutions déclarées

Les domaines associés

Click Chemistry and ApplicationsMonoclonal and Polyclonal Antibodies ResearchChemical Synthesis and AnalysisMedical Imaging Techniques and ApplicationsRadiopharmaceutical Chemistry and Applications

Les publications récentes

Accès ouvert 2025 article OpenAlex

trans -Cyclooctene-caged-IL-1β immunocytokine-constructs ligated to unmodified nanobodies allow click-2-release-based control of cytokine activity

Diana Torres‐García, M. Thierry Shema, Alexi J. C. Sarris, Shimrit David et autres

Click-triggered reactivation of caged cytokine constructs at the tumour site via a Diels–Alder–pyridazine-elimination cascade restores signalling and immune activation. This approach reduces systemic toxicity of immunocytokine therapies.

nl, at, gb (code pays fourni par la source)

4 citations RSC Chemical Biology
Accès ouvert 2024 article OpenAlex

Cover Picture: Transforming Aryl‐Tetrazines into Bioorthogonal Scissors for Systematic Cleavage of trans‐Cyclooctenes (Angew. Chem. Int. Ed. 5/2025)

Martin Wilkovitsch, Walter Kuba, Patrick Keppel, Barbara Sohr et autres

Bioorthogonal bond-cleavage reactions enable precise control of (bio)molecular function in biological systems. In their Research Article (e202411707), Hannes Mikula et al. report the development of “yellow” hydroxyaryl-tetrazines as bioorthogonal tools for efficient click-to-release of trans-cyclooctenes. The cover picture illustrates the transformation of …

at, us, pl, cz (code pays fourni par la source)

0 citations Angewandte Chemie International Edition
Accès ouvert 2024 article OpenAlex

Titelbild: Hydroxylierte Aryl‐Tetrazine als bioorthogonale Scheren zur systematischen Spaltung von trans‐Cyclooctenen (Angew. Chem. 5/2025)

Martin Wilkovitsch, Walter Kuba, Patrick Keppel, Barbara Sohr et autres

Bioorthogonal bond-cleavage reactions enable precise control of (bio)molecular function in biological systems. In their Research Article (e202411707), Hannes Mikula et al. report the development of “yellow” hydroxyaryl-tetrazines as bioorthogonal tools for efficient click-to-release of trans-cyclooctenes. The cover picture illustrates the transformation of …

at, de, us, pl, cz (code pays fourni par la source)

0 citations Angewandte Chemie
Accès ouvert 2024 article OpenAlex

Transforming Aryl‐Tetrazines into Bioorthogonal Scissors for Systematic Cleavage of trans ‐Cyclooctenes

Martin Wilkovitsch, Walter Kuba, Patrick Keppel, Barbara Sohr et autres

Bioorthogonal bond-cleavage reactions have emerged as a powerful tool for precise spatiotemporal control of (bio)molecular function in the biological context. Among these chemistries, the tetrazine-triggered elimination of cleavable trans-cyclooctenes (click-to-release) stands out due to high reaction rates, versatility, and selectivity. Despite an …

at, us, pl, cz (code pays fourni par la source)

21 citations Angewandte Chemie International Edition
Accès ouvert 2024 article OpenAlex

Hydroxylierte Aryl‐Tetrazine als bioorthogonale Scheren zur systematischen Spaltung von trans ‐Cyclooctenen

Martin Wilkovitsch, Walter Kuba, Patrick Keppel, Barbara Sohr et autres

Abstract Bioorthogonale Bindungsspaltungsreaktionen haben sich als leistungsstarke Werkzeuge für die präzise zeitliche und räumliche Kontrolle (bio)molekularer Funktionen in biologischen Systemen etabliert. Unter diesen sticht die durch Click‐Reaktion mit Tetrazinen ausgelöste Eliminierung spaltbarer trans ‐Cyclooctene (Click‐Spaltung, engl. Click‐to‐Release) aufgrund hoher Reaktionsraten sowie ihrer …

at, de, us, pl, cz (code pays fourni par la source)

2 citations Angewandte Chemie
Accès ouvert 2024 preprint OpenAlex

Transforming Aryl-Tetrazines into Bioorthogonal Scissors for Systematic Cleavage of trans-Cyclooctenes

Martin Wilkovitsch, Walter Kuba, Patrick Keppel, Barbara Sohr et autres

Bioorthogonal bond-cleavage reactions have emerged as a powerful tool for precise spatiotemporal control of (bio)molecular function in the biological context. Among these chemistries, the tetrazine-triggered elimination of cleavable trans-cyclooctenes (click-to-release) stands out due to high reaction rates, versatility, and selectivity. Despite an …

at, us, cz (code pays fourni par la source)

1 citation ChemRxiv
Accès ouvert 2024 preprint OpenAlex

Transforming Aryl-Tetrazines into Bioorthogonal Scissors for Systematic Cleavage of trans-Cyclooctenes

Martin Wilkovitsch, Walter Kuba, Patrick Keppel, Barbara Sohr et autres

Bioorthogonal bond-cleavage reactions have emerged as a powerful tool for precise spatiotemporal control of (bio)molecular function in the biological context. Among these chemistries, the tetrazine-triggered elimination of cleavable trans-cyclooctenes (click-to-release) stands out due to high reaction rates, versatility, and selectivity. Despite an …

at, us, cz (code pays fourni par la source)

0 citations ChemRxiv
Accès ouvert 2024 preprint OpenAlex

Transforming Aryl-Tetrazines into Bioorthogonal Scissors for Systematic Cleavage of trans-Cyclooctenes

Martin Wilkovitsch, Walter Kuba, Patrick Keppel, Barbara Sohr et autres

Bioorthogonal bond-cleavage reactions have emerged as a powerful tool for precise spatiotemporal control of (bio)molecular function in the biological context. Among these chemistries, the tetrazine-triggered elimination of cleavable trans-cyclooctenes (click-to-release) stands out due to high reaction rates, versatility, and selectivity. Despite an …

at, us, cz (code pays fourni par la source)

1 citation ChemRxiv
Accès ouvert 2023 article OpenAlex

Post-radiolabeling thioether oxidation to enhance the bioorthogonal reactivity of 18F-tetrazines

Martin Wilkovitsch, Dennis Svatunek, Hannes Mikula, Christoph Denk

Abstract Radiolabeled 1,2,4,5-tetrazines are powerful heterocyclic agents for bioorthogonal PET imaging due to their fast cycloaddition with trans-cyclooctenes. However, fluorine-18 radiolabeling of highly reactive tetrazines is often not feasible due to limited compound stability. We demonstrate that post-radiolabeling oxidation of thioether functionalities …

at (code pays fourni par la source)

3 citations Monatshefte für Chemie - Chemical Monthly

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