Crosslinking of DNA by busulfan Formation of diguanyl derivatives

William P. Tong, David B. Ludlum

Research output: Contribution to journalArticlepeer-review

61 Scopus citations

Abstract

High-pressure liquid chromatography has been used to separate the derivatives of guanosine which are formed when this nucleoside is reacted with busulfan. Derivatives which have been identified by a combination of ultraviolet and mass spectrometry include: 7-(δ-hydroxybutyl)guanosine, 1,4-di(7-guanosyl)butane, and 1-(7-guanyl)-4-(7-guanosinyl)butane. The latter two derivatives can be converted to 1,4-di(7-guanyl)butane by mild acid hydrolysis. Using 1,4-di(7-guanyl)butane as a marker for high-pressure liquid chromatography, we have identified this compound as a product of the reaction between DNA and busulfan. These findings verify the previously unconfirmed report that busulfan is a crosslinking agent for DNA and strengthen the hypothesis that differences in the biological properties of alkylating agents result from differences in their reactions with DNA.

Original languageEnglish (US)
Pages (from-to)174-181
Number of pages8
JournalBBA Section Nucleic Acids And Protein Synthesis
Volume608
Issue number1
DOIs
StatePublished - Jun 27 1980

Keywords

  • Alkylating agent
  • Antitumor compound
  • Busulfan
  • DNA crosslinking

ASJC Scopus subject areas

  • General Medicine

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