4.5 Article

SAR study of a novel triene-ansamycin group compound, quinotrierixin, and related compounds, as inhibitors of ER stress-induced XBP1 activation - II. Structure elucidation

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JOURNAL OF ANTIBIOTICS
卷 61, 期 5, 页码 312-317

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JAPAN ANTIBIOTICS RESEARCH ASSOC
DOI: 10.1038/ja.2008.44

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triene-ansamycin; ER stress; XBP1

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Four novel triene-ansamycin group compounds, quinotrierixin, demethyltrienomycin A, demethyltrienomycin B and demethyltrienomycinol, were isolated from the culture broth of Streptomyces sp. PAE37 as inhibitors of ER stress-induced XBP1 activation. The structures of quinotrierixin, demethyltrienomycin A, demethyltrienomycin B and demethyltrienomycinol were determined on the basis of their spectroscopical and chemical properties. All of four possessed 21-membered macrocyclic lactams including triene moieties.

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