Abstract
Dynamic combinatorial chemistry (DCC) represents an approach, whereby traditional supramolecular scaffolds used for protein surface recognition might be exploited to achieve selective high affinity target recognition. Synthesis, in situ screening and amplification under selection pressure allows the generation of ligands, which bear different moieties capable of making multivalent non-covalent interactions with target proteins. Generic tetracarboxyphenyl porphyrin scaffolds bearing four hydrazide moieties have been used to form dynamic combinatorial libraries (DCLs) using aniline-catalyzed reversible hydrazone exchange reactions, in 10 % DMSO, 5 mm NH4OAc, at pH 6.75. High resolution mass spectrometry (HRMS) was used to monitor library composition and establish conditions under which equilibria were established.
Original language | English |
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Pages (from-to) | 1872-1879 |
Number of pages | 8 |
Journal | European Journal of Organic Chemistry |
Volume | 2018 |
Issue number | 16 |
DOIs | |
Publication status | Published - 30 Apr 2018 |
Bibliographical note
Funding Information:This work was supported by the Engineering and Physical Sciences Research Council [EP/L504993/1, EP/K039202/1 and EP/N013573/1] and the Wellcome Trust [097827/Z/11/A]
Publisher Copyright:
© 2018 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA.
Keywords
- Dynamic combinatorial chemistry
- Hydrazones
- Porphyrins
- Protein surface mimetics
ASJC Scopus subject areas
- Physical and Theoretical Chemistry
- Organic Chemistry