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Modular triazine-based carborane-containing carboxylic acids - synthesis and characterisation of potential boron neutron capture therapy agents made of readily accessible building blocks.

Martin KellertDennis J WormPaul HoppenzMenyhárt-Botond SárosiPeter LönneckeBernd RiedlJohannes KoebberlingAnnette G Beck-SickingerEvamarie Hey-Hawkins
Published in: Dalton transactions (Cambridge, England : 2003) (2019)
Based on a modular combination of s-triazine, the well-known 9-mercapto-1,7-dicarba-closo-dodecaborane(12) and commercially available carboxylic acids, namely thioglycolic acid, glycine, and Nα-Boc-l-lysine, several carboxylic acid derivatives were synthesised and fully characterised. The thioglycolic acid derivative was introduced into a peptide hormone by solid phase peptide synthesis. High activity and selective internalisation into peptide receptor-expressing cells was observed. With a very high boron content of twenty boron atoms, these derivatives are interesting as selective Boron Neutron Capture Therapy (BNCT) agents.
Keyphrases
  • induced apoptosis
  • cell cycle arrest
  • stem cells
  • oxidative stress
  • cell proliferation
  • bone marrow
  • solid phase extraction
  • mass spectrometry
  • endoplasmic reticulum stress
  • high resolution
  • pi k akt
  • liquid chromatography