Bahou, Calise;
Chudasama, Vijay;
(2022)
The use of bromopyridazinedione derivatives in chemical biology.
Organic & Biomolecular Chemistry
10.1039/d2ob00310d.
(In press).
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Abstract
Tools that facilitate the chemical modification of peptides and proteins are gaining an increasing amount of interest across many avenues of chemical biology as they enable a plethora of therapeutic, imaging and diagnostic applications. Cysteine residues and disulfide bonds have been highlighted as appealing targets for modification due to the highly homogenous nature of the products that can be formed through their site-selective modification. Amongst the reagents available for the site-selective modification of cysteine(s)/disulfide(s), pyridazinediones (PDs) have played a particularly important and enabling role. In this review, we outline the unique chemical features that make PDs especially well-suited to cysteine/disulfide modification on a wide variety of proteins and peptides, as well as provide context as to the problems solved (and applications enabled) by this technology.
Type: | Article |
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Title: | The use of bromopyridazinedione derivatives in chemical biology |
Location: | England |
Open access status: | An open access version is available from UCL Discovery |
DOI: | 10.1039/d2ob00310d |
Publisher version: | https://doi.org/10.1039/D2OB00310D |
Language: | English |
Additional information: | © Royal Society of Chemistry 2022. This article is licensed under a Creative Commons Attribution 3.0 Unported Licence (http://creativecommons.org/licenses/by/3.0/). |
UCL classification: | UCL > Provost and Vice Provost Offices > UCL BEAMS > Faculty of Maths and Physical Sciences UCL > Provost and Vice Provost Offices > UCL BEAMS > Faculty of Maths and Physical Sciences > Dept of Chemistry UCL > Provost and Vice Provost Offices > UCL BEAMS UCL |
URI: | https://discovery.ucl.ac.uk/id/eprint/10146807 |
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