Redox-active lipid-incorporating proteins as a novel immobilisation technique
References (31)
- et al.
J. Inorg. Biochem.
(1995) - et al.
Inorg. Chem. Acta
(1996) Micron
(1993)- et al.
J. Mol. Biol.
(1990) - et al.
J. Electroanal. Chem.
(1990) - et al.
Appl. Surf. Sci.
(1992) - et al.
Biochim. Biophys. Acta
(1992) - et al.
J. Electroanal. Chem.
(1996) - et al.
Membranes and Molecular Assemblies: The Synkinetic Approach
(1994) - et al.
Micelles, Monolayers and Biomembranes
(1995)
Membrane Mimetic Chemistry
J. Am. Chem. Soc.
Chem. Ind.
Science
Biochim. Biophys. Acta
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Synthesis of amphiphilic seleninic acid derivatives with considerable activity against cellular membranes and certain pathogenic microbes
2014, Journal of Hazardous MaterialsCitation Excerpt :Importantly, O-sulfation has been achieved with the use of chlorosulfonic acid, and this final step required to introduce the hydrophilic head group can lead to an overall damage and subsequent instability of the molecule in question (including hydrolysis of the sulfate head group). Indeed, the use of common hydrophilic head groups, such as a sulfate, phosphate or ammonium group, poses certain challenges as far as their introduction and subsequent chemical stability are concerned (carboxylic acids are easier to use but often of insufficient hydrophilicity) [19–22]. As part of this study, we have therefore explored the use of a seleninic acid as ‘head’ group as elegant alternative to conventional approaches, hence removing the need for a separate hydrophilic head and, at the same time, endowing the head with considerable (thiol-)specific chemical reactivity (Fig. 1).
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1998, Journal of Chemical Research - Part S