Abstract
A series of palmarumycin prodrugs and water-soluble analogs has been synthesized and assayed for inhibition of the thioredoxin-thioredoxin reductase system. Increased aqueous solubility led to an improved in vivo activity profile.
Original language | English (US) |
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Pages (from-to) | 3880-3882 |
Number of pages | 3 |
Journal | Organic and Biomolecular Chemistry |
Volume | 3 |
Issue number | 21 |
DOIs | |
State | Published - Nov 7 2005 |
ASJC Scopus subject areas
- Biochemistry
- Physical and Theoretical Chemistry
- Organic Chemistry