Literature DB >> 17665367

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

Tali Ashkenazi1, Dalia Pinkert, Ayelet Nudelman, Ayala Widberg, Barry Wexler, Vernon Wittenbach, Dennis Flint, Abraham Nudelman.   

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 GR(50) (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). Society of Chemical Industry

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Year:  2007        PMID: 17665367     DOI: 10.1002/ps.1427

Source DB:  PubMed          Journal:  Pest Manag Sci        ISSN: 1526-498X            Impact factor:   4.845


  2 in total

1.  Structural characterization of the Mycobacterium tuberculosis biotin biosynthesis enzymes 7,8-diaminopelargonic acid synthase and dethiobiotin synthetase .

Authors:  Sanghamitra Dey; James M Lane; Richard E Lee; Eric J Rubin; James C Sacchettini
Journal:  Biochemistry       Date:  2010-08-10       Impact factor: 3.162

2.  A bifunctional locus (BIO3-BIO1) required for biotin biosynthesis in Arabidopsis.

Authors:  Rosanna Muralla; Elve Chen; Colleen Sweeney; Jennifer A Gray; Allan Dickerman; Basil J Nikolau; David Meinke
Journal:  Plant Physiol       Date:  2007-11-09       Impact factor: 8.340

  2 in total

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