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Structure, synthesis, and antitumor activity of the hydrolysis product of the antitumor agent carmethizole

  • Wayne K. Anderson
  • , D. Michael Houston
  • , Mark A. Jarosinski
  • , Frederick R. Kinder
  • , Rao N. Kode
  • , Patrick Van Roey
  • , Jeffrey M. Salerno
  • SUNY Buffalo
  • Hauptman-Woodward Medical Research Institute, Inc.

Research output: Contribution to journalArticlepeer-review

Abstract

The two isomeric monocarbamates, 2b and 2c, related to the antitumor drug carmethizole (1) were synthesized and the structure of the carmethizole hydrolysis product, 2b, was established by X‐ray crystallography. The chemical reactivity, toxicity, and antitumor activity of the two monocarbamates, 2b and 2c, were compared with 1. © 1993 wiley‐Liss, Inc.

Original languageEnglish
Pages (from-to)143-146
Number of pages4
JournalDrug Development Research
Volume30
Issue number3
DOIs
StatePublished - Nov 1993

Keywords

  • anticancer
  • carmethizole
  • hydrolysis
  • toxicity

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