Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/34859
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Type: Journal article
Title: The preparation of side chain functionalized analogues of coenzyme Q for protein conjugation studies
Author: Daines, A.
Abell, A.
Citation: Organic and Biomolecular Chemistry, 2004; 2(16):2371-2375
Publisher: Royal Soc Chemistry
Issue Date: 2004
ISSN: 1477-0520
1477-0539
Abstract: The synthesis of two analogues of CoQ ( 10 and 13) suitable for conjugation to a peptide or protein, and hence the development of an ELISA immunoassay, is presented. These analogues were synthesized from the protected quinone, 1-bromo-2-methyl-3,4,5,6-tetramethoxybenzene ( 1), itself prepared from commercially available CoQ-0 ( 3). Model coupling studies of one of the analogues ( 10) to N-acetyl-L-lysine methyl ester and a lysine containing dipeptide (N-acetyl-glycine-L-lysine methyl ester) were also undertaken as a first step to monoclonial antibody production.
Keywords: Ubiquinone
Proteins
Molecular Structure
Protein Binding
DOI: 10.1039/b407659a
Appears in Collections:Aurora harvest 6
Chemistry publications

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