Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1369314 | Bioorganic & Medicinal Chemistry Letters | 2014 | 4 Pages |
Abstract
A cyclic form of N6-threonylcarbamoyladenosine bearing an oxazolone moiety (ct6A) was discovered very recently at the position 37 in several tRNA sequences. Our study on the synthesized 5′,3′,2′-O-acetylated derivative of ct6A confirmed high stability of the modified nucleoside under physiological conditions (PBS buffer, pH 7.4) and revealed remarkable stability of the oxazolone ring in acidic (100 mM HCl, pH 1) and basic (0.1 mM NaOH, pH 10) conditions. This feature may allow for the post-synthetic conversion of t6A into ct6A in assembled oligoribonucleotides.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Michal Matuszewski, Elzbieta Sochacka,