Abstract
Syntheses and physicochemical properties are described of several novel naphthoquinonyl amino acid derivatives, which are potential components in cytotoxic peptide conjugates. These compounds include Nε- and Nα -naphthoquinonyl derivatives of lysine as well as N-naphthoquinonyl-carboxylic derivatives. The former class of compounds can be employed as building blocks in a stepwise peptide synthesis, whereas the latter two are adequate for postpeptide chain-assembly modifications. The ability of the naphthoquinonyl derivatives to produce semiquinone radicals and hydroxyl radicals (OH), using chemical (i.e. NaBH4) and enzymatic (i.e. NADPH-cytochrome P-450 reductase) routes, respectively, was evaluated employing electron spin resonance spectroscopy.
| Original language | English |
|---|---|
| Pages (from-to) | 263-274 |
| Number of pages | 12 |
| Journal | International Journal of Peptide Research and Therapeutics |
| Volume | 3 |
| Issue number | 5 |
| DOIs | |
| State | Published - 1996 |
| Externally published | Yes |
Keywords
- Cytotoxic peptides
- ESR
- Quinones
- Reactive oxygen species
- Targeted chemotherapy
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