Large-scale, protection-free synthesis of Se-adenosyl-l-selenomethionine analogues and their application as cofactor surrogates of methyltransferases Journal Article


Authors: Bothwell, I. R.; Luo, M.
Article Title: Large-scale, protection-free synthesis of Se-adenosyl-l-selenomethionine analogues and their application as cofactor surrogates of methyltransferases
Abstract: S-Adenosyl-l-methionine (SAM) analogues have previously demonstrated their utility as chemical reporters of methyltransferases. Here we describe the facile, large-scale synthesis of Se-alkyl Se-adenosyl-l-selenomethionine (SeAM) analogues and their precursor, Se-adenosyl-l-selenohomocysteine (SeAH). Comparison of SeAM analogues with their equivalent SAM analogues suggests that sulfonium-to-selenonium substitution can enhance their compatibility with certain protein methyltransferases, favoring otherwise less reactive SAM analogues. Ready access to SeAH therefore enables further application of SeAM analogues as chemical reporters of diverse methyltransferases. © 2014 American Chemical Society.
Journal Title: Organic Letters
Volume: 16
Issue: 11
ISSN: 1523-7060
Publisher: American Chemical Society  
Date Published: 2014-05-22
Start Page: 3056
End Page: 3059
Language: English
DOI: 10.1021/ol501169y
PROVIDER: scopus
PMCID: PMC4059250
PUBMED: 24852128
DOI/URL:
Notes: Org. Lett. -- Export Date: 8 July 2014 -- CODEN: ORLEF -- Source: Scopus
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  1. Minkui Luo
    70 Luo