Skip to main navigation Skip to search Skip to main content

Novel naphthoquinonyl derivatives: Potential structural components for the synthesis of cytotoxic peptides

  • Shai Rahimipour
  • , Lev Weiner
  • , Mali Fridkin
  • , Prativa Bade Shrestha-Dawadi
  • , Shmuel Bittner
  • Weizmann Institute of Science
  • Ben-Gurion University of the Negev

Research output: Contribution to journal › Article › peer-review

26 Scopus citations

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 languageEnglish
Pages (from-to)263-274
Number of pages12
JournalInternational Journal of Peptide Research and Therapeutics
Volume3
Issue number5
DOIs
StatePublished - 1996
Externally publishedYes

Keywords

  • Cytotoxic peptides
  • ESR
  • Quinones
  • Reactive oxygen species
  • Targeted chemotherapy

Fingerprint

Dive into the research topics of 'Novel naphthoquinonyl derivatives: Potential structural components for the synthesis of cytotoxic peptides'. Together they form a unique fingerprint.

Cite this