Ranasinghe Rohan T, Rusling David A, Powers Vicki E C, Fox Keith R, Brown Tom
School of Chemistry, University of Southampton, Highfield, Southampton, UK SO17 1BJ.
Chem Commun (Camb). 2005 May 28(20):2555-7. doi: 10.1039/b502325d. Epub 2005 Apr 14.
Substituted 3H-pyrrolo[2,3-d]pyrimidin-2(7H)-one nucleoside analogues have been synthesised from 5-alkynyl-uridine derivatives, incorporated into triplex forming oligonucleotides (TFOs) and found to selectively bind CG inversions with enhanced affinity compared to T.
已从5-炔基尿苷衍生物合成了取代的3H-吡咯并[2,3-d]嘧啶-2(7H)-酮核苷类似物,将其掺入三链形成寡核苷酸(TFO)中,发现与T相比,它们能以更高的亲和力选择性结合CG倒位。