Published August 20, 2009
| Accepted Version + Supplemental Material
Journal Article
Open
Oligomerization Route to Py-Im Polyamide Macrocycles
Chicago
Abstract
Cyclic eight-ring pyrrole−imidazole polyamides are sequence-specific DNA-binding small molecules that are cell permeable and can regulate endogenous gene expression. Syntheses of cyclic polyamides have been achieved by solid-phase and solution-phase methods. A rapid solution-phase oligomerization approach to eight-ring symmetrical cyclic polyamides yields 12- and 16-membered macrocycles as well. A preference for DNA binding by the 8- and 16-membered oligomers was observed over the 12-ring macrocycle, which we attributed to a conformational constraint not present in the smaller and larger systems.
Additional Information
© 2009 American Chemical Society. Received June 11, 2009. Publication Date (Web): July 23, 2009. This work was supported by the National Institutes of Health (GM27681). D.M.C. is grateful for a Caltech Kanel predoctoral fellowship. D.A.H. thanks the California Tobacco-Related Disease Research Program (16FT-0055) for a postdoctoral fellowship.Attached Files
Accepted Version - nihms134644.pdf
Supplemental Material - Chenowethol901311m_si_001.pdf
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Chenowethol901311m_si_001.pdf
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Additional details
- PMCID
- PMC2736337
- Eprint ID
- 15320
- Resolver ID
- CaltechAUTHORS:20090826-112850226
- NIH
- GM-27681
- Kanel Foundation
- California Tobacco-Related Disease Research Program
- 16FT-0055
- Created
-
2009-09-11Created from EPrint's datestamp field
- Updated
-
2021-11-08Created from EPrint's last_modified field