| Literature DB >> 28433513 |
John T Gupton1, Scott Yeudall2, Nakul Telang2, Megan Hoerrner2, Ellis Huff2, Evan Crawford2, Katie Lounsbury2, Michael Kimmel2, William Curry2, Andrew Harrison2, Wen Juekun2, Alex Shimozono2, Joe Ortolani2, Kristin Lescalleet2, Jon Patteson2, Veronica Moore-Stoll2, Cristina C Rohena3, Susan L Mooberry3, Ahmad J Obaidullah4, Glen E Kellogg4, James A Sikorski5.
Abstract
New microtubule depolymerizing agents with potent cytotoxic activities have been prepared with a 5-cyano or 5-oximino group attached to a pyrrole core. The utilization of ortho activation of a bromopyrrole ester to facilitate successful Suzuki-Miyaura cross-coupling reactions was a key aspect of the synthetic methodology. This strategy allows for control of regiochemistry with the attachment of four completely different groups at the 2, 3, 4 and 5 positions of the pyrrole scaffold. Biological evaluations and molecular modeling studies are reported for these examples.Entities:
Keywords: Cytotoxic activity; Marine natural products; Microtubule inhibitors; Pyrrole; Suzuki-Miyaura cross-coupling
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Year: 2017 PMID: 28433513 PMCID: PMC5517042 DOI: 10.1016/j.bmc.2017.04.012
Source DB: PubMed Journal: Bioorg Med Chem ISSN: 0968-0896 Impact factor: 3.641