Journal
ORGANIC LETTERS
Volume 8, Issue 21, Pages 4855-4858Publisher
AMER CHEMICAL SOC
DOI: 10.1021/ol061918j
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Funding
- NCI NIH HHS [CA109265] Funding Source: Medline
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[GRAPHICS] The coumarin antibiotics are not only potent inhibitors of DNA gyrase but also represent the most effective C-terminal inhibitors of 90 kDa heat shock proteins (Hsp90) reported thus far. In contrast to the N-terminal ATP-binding site, little is known about the Hsp90 C-terminus. In addition, very limited structure-activity relationships exist between this class of natural products and Hsp90. In this letter, the syntheses of dimeric coumarin analogues are presented along with their inhibitory values in breast cancer cell lines.
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