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      Potent non-benzoquinone ansamycin heat shock protein 90 inhibitors from genetic engineering of Streptomyces hygroscopicus.

      Journal of Medicinal Chemistry
      Calorimetry, Cell Division, drug effects, Cell Line, Tumor, Genetic Engineering, HSP90 Heat-Shock Proteins, antagonists & inhibitors, Humans, Rifabutin, pharmacology, Streptomyces, genetics

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          Abstract

          Inhibition of the protein chaperone Hsp90 is a promising new approach to cancer therapy. We describe the preparation of potent non-benzoquinone ansamycins. One of these analogues, generated by feeding 3-amino-5-chlorobenzoic acid to a genetically engineered strain of Streptomyces hygroscopicus, shows high accumulation and long residence time in tumor tissue, is well-tolerated upon intravenous dosing, and is highly efficacious in the COLO205 mouse tumor xenograft model.

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