Search Results - "Dobler, Markus R"
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Investigating the Structure-Activity Relationship of the Insecticidal Natural Product Rocaglamide
Published in Chimia (01-12-2017)“…The natural product Rocaglamide (1), isolated from the tree Aglaia elliptifolia, is a compelling but also challenging lead structure for crop protection. In…”
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Human HDAC isoform selectivity achieved via exploitation of the acetate release channel with structurally unique small molecule inhibitors
Published in Bioorganic & medicinal chemistry (01-08-2011)“…[Display omitted] ► Amino-acid derived HDAC8 small molecule inhibitors. ► α-Amino-ketone Zn binding allows synthetic access to the acetate release channel. ►…”
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Identification of Orally Available Naphthyridine Protein Kinase D Inhibitors
Published in Journal of medicinal chemistry (12-08-2010)“…A novel 2,6-naphthyridine was identified by high throughput screen (HTS) as a dual protein kinase C/D (PKC/PKD) inhibitor. PKD inhibition in the heart was…”
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4
Synthesis and fungicidal activity of tubulin polymerisation promoters. Part 1: pyrido[2,3-b]pyrazines
Published in Pest management science (01-02-2010)“…BACKGROUND: The excellent fungicidal activity of [1,2,4]triazolo[1,5-a]pyrimidines suggested the search for further analogues with improved properties.RESULTS:…”
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Design and novel synthesis of aryl-heteroaryl-imidazole MAP kinase inhibitors
Published in Tetrahedron letters (15-09-2003)“…Inhibitors of the MAP kinase p38, potentially useful for the treatment of rheumatoid arthritis and inflammatory diseases, were found to exhibit antifungal…”
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Total synthesis of (±)-rocaglamide and some aryl analogues
Published in Tetrahedron letters (19-11-2001)“…The insecticidal activity found for rocaglamide and its congeners, prompted us to establish a short and efficient synthesis of the natural product and some…”
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Total synthesis of (+)-epopromycin B and its analogues—studies on the inhibition of cellulose biosynthesis
Published in Tetrahedron letters (08-01-2001)“…The described inhibition of the cellulose biosynthesis by epopromycin B prompted us to establish a short and efficient synthesis of the natural product,…”
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