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Aryl chain analogues of the biotin vitamers as potential herbicides. Part 3

  • Tali Ashkenazi
  • , Dalia Pinkert
  • , Ayelet Nudelman
  • , Ayala Widberg
  • , Barry Wexler
  • , Vernon Wittenbach
  • , Dennis Flint
  • , Abraham Nudelman
  • Bar-Ilan University
  • DuPont

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

7 Scopus citations

Abstract

Novel aryl chain isosters and analogues of 7-keto-8-aminopelargonic acid (KAPA) and 7,8-diaminopelargonic acid (DAPA), the vitamer intermediates involved in the biosynthetic pathway of biotin, possessing chain lengths of eight carbon atoms, were prepared and evaluated as potential herbicides. In the greenhouse test the most active compounds were the fluorinated derivative 9d and the selenophenyl/furan mixture 17m/17p, which were most active against Foxtail millet. In the more sensitive Arabidopsis test the most active substances were 9a and 17m, which displayed GR50 (concentration of active compound causing 50% growth inhibition) values of 0.2 and 0.5 mg kg-1 respectively (values of <50 mg kg-1 are considered herbicidal).

Original languageEnglish
Pages (from-to)974-1001
Number of pages28
JournalPest Management Science
Volume63
Issue number10
DOIs
StatePublished - Oct 2007

Keywords

  • Biotin
  • Biotin vitamers
  • Enzyme inhibition
  • Herbicides
  • Isosters

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