Organic & Biomolecular Chemistry · 2004 · 66 citations · 27 references
PharmacyMedicinal ChemistryPharmacologyDrug DesignDrug DiscoverySynthetic Medicinal ChemistryEnzyme InhibitionNatural Product Drug DiscoveryNatural Product-based Drug DesignPotency OptimizationStructure-activity Relationship AnalysisThioredoxin SystemCell Potency AssaysCell-based AssaysNatural Product BioactivityNatural Product PharmacologyNatural Product SynthesisRedox ControlThioredoxin Reductase System
Spiroketal naphthodecalins are readily assembled by Barton's base mediated Ullmann binaphthyl ether coupling, Dakin reactions and hypervalent iodine spirocyclization. The core structures can be further diversified by enone addition and Stille coupling reactions. Nanomolar inhibitors for the Trx/TrxR redox control system were prepared by this approach and compared to series of natural product isolates. Cytotoxicity in MCF-7 cell assays ranged from an IC50 of 1.6 to >100 microM.
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Human Placenta Thioredoxin Reductase
Stephan Gromer, L. David Arscott, Charles H. Williams et al. · Journal of Biological Chemistry · 1998 · 535 citations · Full text
Sarah J. Welsh, William Bellamy, Margaret M. Briehl et al. · PubMed · 2002 · 349 citations
Medicine, Biochemistry, Oncology +17