Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Matthias Tanriver"'
Autor:
Darja Beyer, Christian Vaccarin, Xavier Deupi, Ana Katrina Mapanao, Susan Cohrs, Fan Sozzi-Guo, Pascal V. Grundler, Nicholas P. van der Meulen, Jinling Wang, Matthias Tanriver, Jeffrey W. Bode, Roger Schibli, Cristina Müller
Publikováno v:
EJNMMI Research, Vol 13, Iss 1, Pp 1-14 (2023)
Abstract Purpose The angiotensin converting enzyme-2 (ACE2)—entry receptor of SARS-CoV-2—and its homologue, the angiotensin-converting enzyme (ACE), play a pivotal role in maintaining cardiovascular homeostasis. Potential changes in ACE2 expressi
Externí odkaz:
https://doaj.org/article/ad4f974295474f0392325fbd07ff6ab8
The role of monoclonal antibodies as vehicles to deliver payloads has evolved as a powerful tool in cancer therapy in recent years. The clinical development of therapeutic antibody-conjugates with precise payloads holds great promise for targeted the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6458dfc7d0404c28c47b9ad8e3255fef
https://doi.org/10.26434/chemrxiv-2023-4f6kr
https://doi.org/10.26434/chemrxiv-2023-4f6kr
Autor:
Anissa Ouald Chaib, Alessandro Fracassi, Ankita Ray, Dominik Schauenburg, Nako Nakatsuka, Antonella Rossi, Jeffrey W. Bode, Matthias Tanriver, Simon Scherrer, Yoko Yamakoshi, Cristiana Passiu, Joydeb Mandal, Nicholas D. Spencer, Shivaprakash N. Ramakrishna
Publikováno v:
ACS Applied Materials & Interfaces. 13:29113-29121
The efficient and bioorthogonal chemical ligation reaction between potassium acyltrifluoroborates (KATs) and hydroxylamines (HAs) was used for the surface functionalization of a self-assembled monolayer (SAM) with biomolecules. An alkane thioether mo
Publikováno v:
Angewandte Chemie. 132:16993-17004
Acylboron compounds are emerging as versatile functional groups with applications in multiple research fields. Their synthesis, however, is still challenging and requires innovative methods. This Minireview provides an overview on the obstacles of ac
Autor:
Thomas Betzel, Matthias Tanriver, Haewon Song, Roger Schibli, Jeffrey W. Bode, Christopher J. White, Aristeidis Chiotellis, Hazem Ahmed, Simon M. Ametamey, Sara Da Ros
Publikováno v:
Chemical Communications. 56:723-726
A new prosthetic group is reported for 18F-labelling of peptides and proteins based on the chemoselective ligation of potassium acyltrifluoroborates (KATs) and hydroxylamines without any detectable 18F/19F isotope exchange at the acyltrifluoroborate
Potassium acyltrifluoroborates (KATs) undergo chemoselective amide-forming ligations with hydroxylamines. Under aqueous, acidic conditions these ligations can proceed rapidly, with rate constants of ~20 M-1 s-1. The requirement for lower pH to obtain
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8207907add40d6ef54f3435b9a41b00a
https://doi.org/10.26434/chemrxiv.14474166.v1
https://doi.org/10.26434/chemrxiv.14474166.v1
Autor:
Shivaprakash N. Ramakrishna, Simon Scherrer, Ankita Ray, Nako Nakatsuka, Matthias Tanriver, Yoko Yamakoshi, Cristiana Passiu, Jeffrey W. Bode, Dominik Schauenburg, Alessandro Fracassi, Antonella Rossi, Nicholas D. Spencer
The efficient and bioorthogonal chemical ligation reaction between potassium acyltrifluoroborates (KATs) and hydroxylamines (HAs) was used for the surface functionalizationof a self-assembled monolayer (SAM) with biomolecules. An alkane thioether mol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::176e63d0a4ca549e93711dafe7b44846
https://doi.org/10.26434/chemrxiv.14315615.v1
https://doi.org/10.26434/chemrxiv.14315615.v1
Autor:
Aristeidis, Chiotellis, Hazem, Ahmed, Thomas, Betzel, Matthias, Tanriver, Christopher J, White, Haewon, Song, Sara, Da Ros, Roger, Schibli, Jeffrey W, Bode, Simon M, Ametamey
Publikováno v:
Chemical communications (Cambridge, England). 56(5)
A new prosthetic group is reported for 18F-labelling of peptides and proteins based on the chemoselective ligation of potassium acyltrifluoroborates (KATs) and hydroxylamines without any detectable 18F/19F isotope exchange at the acyltrifluoroborate