4.8 Article

Solution-Phase Synthesis of Pyrrole-Imidazole Polyamides

Journal

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 131, Issue 20, Pages 7175-7181

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ja901307m

Keywords

-

Funding

  1. National Institutes of Health [GM27681]
  2. Caltech Kanel predoctoral fellowship
  3. California TobaccoRelated Disease Research Program [16FT-0055]
  4. The National Science Foundation Chemistry Research Inst umentation and Facilities Program [CHE-0541745]
  5. UPLC-MS instrument

Ask authors/readers for more resources

Pyrrole-Imidazole polyamides are DNA-binding molecules that are programmable for a large repertoire of DNA sequences. Typical syntheses of this class of heterocyclic oligomers rely on solid-phase methods. Solid-phase methodologies offer rapid assembly on a micromole scale sufficient for biophysical characterizations and cell culture studies. In order to produce gram-scale quantities necessary for efficacy studies in animals, polyamides must be readily synthesized in solution. An 8-ring hairpin polyamide 1, which targets the DNA sequence 5'-WGWWCW-3', was chosen for our synthesis studies as this oligomer exhibits androgen receptor antagonism in cell culture models of prostate cancer. A convergent solution-phase synthesis of 1 from a small set of commercially available building blocks is presented which highlights principles for preparing gram quantities of pyrrole-imidazole oligomers with minimal chromatography.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.8
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available