| Literature DB >> 26192344 |
Subham Saha1, Anil P Jagtap, Snorri Th Sigurdsson.
Abstract
Two aromatic isothiocyanates, derived from isoindoline nitroxides, were synthesized and selectively reacted with 2'-amino groups in RNA. The spin labels displayed limited mobility in RNA, making them promising candidates for distance measurements by pulsed EPR. After conjugation to RNA, a tetraethyl isoindoline derivative showed significant stability under reducing conditions.Entities:
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Year: 2015 PMID: 26192344 DOI: 10.1039/c5cc05014f
Source DB: PubMed Journal: Chem Commun (Camb) ISSN: 1359-7345 Impact factor: 6.222