| Literature DB >> 23937256 |
Stephen Hanessian1, Jernej Wagger, Bradley L Merner, Robert D Giacometti, Michael E Ostergaard, Eric E Swayze, Punit P Seth.
Abstract
A constrained tricyclic analogue of α-L-LNA (2), which contains dual modes of conformational restriction about the ribose sugar moiety, has been synthesized and characterized by X-ray crystallography. Thermal denaturation experiments of oligonucleotide sequences containing this tricyclic α-L-LNA analogue (α-L-TriNA 2, 5) indicate that this modification is moderately stabilizing when paired with complementary DNA and RNA, but less stabilizing than both α-L-LNA (2) and α-L-TriNA 1 (4).Entities:
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Year: 2013 PMID: 23937256 DOI: 10.1021/jo401170y
Source DB: PubMed Journal: J Org Chem ISSN: 0022-3263 Impact factor: 4.354