Genome-Based Characterization of Two Prenylation Steps in the Assembly of the Stephacidin and Notoamide Anticancer Agents in a Marine-Derived <i>Aspergillus</i> sp.
Yousong Ding(University of Michigan), David H. Sherman(University of Michigan), Jeffrey R. de Wet(University of Michigan), Jennifer M. Finefield(University of Michigan), James D. Sunderhaus(University of Michigan), Sachiko Tsukamoto(Kumamoto University), Shengying Li(University of Michigan), Kenneth A. Miller(Colorado State University), Thomas J. Greshock(University of Michigan), Robert M. Williams(University of Louisville), Timothy McAfoos(University of Michigan), James D. Cavalcoli(University of Michigan)
Cited by 125
Related Papers
Notoamides A–D: Prenylated Indole Alkaloids Isolated from a Marine‐Derived Fungus, <i>Aspergillus</i> sp.
|Angewandte Chemie International Edition|2007|271
Isolation, Structure Elucidation, and Biomimetic Total Synthesis of Versicolamide B, and the Isolation of Antipodal (−)‐Stephacidin A and (+)‐Notoamide B from <i>Aspergillus versicolor</i> NRRL 35600
|Angewandte Chemie International Edition|2008|247
Asymmetric total syntheses of (+)- and (−)-versicolamide B and biosynthetic implications
|Nature Chemistry|2009|153
Discovery of a 3-(4-Pyrimidinyl) Indazole (MLi-2), an Orally Available and Selective Leucine-Rich Repeat Kinase 2 (LRRK2) Inhibitor that Reduces Brain Kinase Activity
|Journal of Medicinal Chemistry|2017|147
Notoamides F−K, Prenylated Indole Alkaloids Isolated from a Marine-Derived <i>Aspergillus</i> sp.
|Journal of Natural Products|2008|133