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The design, synthesis and evaluation of hypoxia-activated pro-oligonucleotides.

Abstract
Hypoxia-activated pro-oligonucleotides were synthesized through the commercial phosphoramidite method, and could be readily cleaved to form normal oligos with good hypoxia selectivity in vitro under the effect of reductases, as well as in tumor cell extract.
AuthorsNan Zhang, Chunyan Tan, Puqin Cai, Peizhuo Zhang, Yufen Zhao, Yuyang Jiang
JournalChemical communications (Cambridge, England) (Chem Commun (Camb)) Issue 22 Pg. 3216-8 (Jun 14 2009) ISSN: 1359-7345 [Print] England
PMID19587918 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Oligonucleotides
  • Prodrugs
  • Nitroreductases
  • Fluorescein
Topics
  • Animals
  • Base Sequence
  • Cattle
  • Drug Design
  • Escherichia coli (enzymology)
  • Fluorescein (metabolism)
  • HeLa Cells
  • Humans
  • Hypoxia
  • Nitroreductases (metabolism)
  • Oligonucleotides (chemical synthesis, chemistry, genetics, metabolism)
  • Prodrugs (chemical synthesis, chemistry, metabolism)
  • Staining and Labeling

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