http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-03048191-A3

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filingDate 2002-12-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c9d1db219320fbc7bae311287b4fd810
publicationDate 2003-12-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber WO-03048191-A3
titleOfInvention Process for the selective alkylation of -sh groups in proteins and peptides for the study of complex protein mixtures
abstract Weakly basic molecules containing a double bond (in particular vinylpyridines) are able to react and selectively alkylate -SH groups in proteins, thus preventing their re-oxidation to disulphur bridges. Contrary to conventional alkylating agents, such as iodoacetamide, such molecules reach 100% alkylation of all -SH residues, even in complex proteins, without reacting with other functional groups. Their use is particularly effective in proteome analysis and more generally for analysing proteins in which the -SH groups should be blocked. Additionally, the use of vinylpyridines partially or totally deuterated, and thus with a mass difference as compared to non-deuterated vinylpyridines, allows studies of induction/repression of protein synthesis.
priorityDate 2001-12-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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Total number of triples: 25.