4.7 Article

Cytotoxic Indolocarbazoles from Actinomadura melliaura ATCC 39691

Journal

JOURNAL OF NATURAL PRODUCTS
Volume 78, Issue 7, Pages 1723-1729

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.jnatprod.5b00429

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Funding

  1. University of Kentucky College of Pharmacy
  2. University of Kentucky Markey Cancer Center
  3. National Center for Advancing Translational Sciences [UL1TR000117]

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Actinomadura melliaura ATCC 39691, a strain isolated from a soil sample collected in Bristol Cove, California, is a known producer of the disaccharide-substituted AT2433 indolocarbazoles (6-9). Reinvestigation of this strain using new media conditions led to >40-fold improvement in the production of previously reported AT2433 metabolites and the isolation and structure elucidation of the four new analogues, AT2433-A3, A4, AS, and B3 (1-4). The availability of this broader set of compounds enabled a subsequent small antibacterial/fungal/cancer SAP. study that revealed disaccharyl substitution, N-6 methylation, and C-11 chlorination as key modulators of bioactivity. The slightly improved anticancer potency of the newly reported N-6-desmethyl 1 (compared to 6) contrasts extensive SAR of monoglycosylated rebeccamycin-type topoisomerase I inhibitors where N-6 alkylation has contributed to improved potency and ADME. Complete 2D NMR assignments for the known metabolite BMY-41219 (5) and C-13 NMR spectroscopic data for the known analogue AT2433-B1 (7) are also provided for the first time.

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