Literature DB >> 24248575

Herbicidal activity of sulforaphene from stock (Matthiola incana).

A M Brinker1, G F Spencer.   

Abstract

A herbicidal compound was isolated from extracts ofMatthiola incana and identified as sulforaphene (4-methylsulfinyl-3-butenyl isothiocyanate). The ED50 of this compound against velvetleaf seedlings was approximately 2×10(-4) M. Glucoraphenin, the glucosinolate that is the natural precursor of sulforaphene, was less phytotoxic, with an ED50 of near 6×10(-3)M.

Entities:  

Year:  1993        PMID： 24248575     DOI： 10.1007/BF00979663

Source DB:  PubMed          Journal:  J Chem Ecol        ISSN： 0098-0331            Impact factor:   2.626


  3 in total

1.  [On the isothiocyanate compounds of Matthiola tristis (L.) R. Br].

Authors:  L CARRERAS MATAS
Journal:  Farmacognosia       Date:  1960 Oct-Dec

2.  Allelochemicals produced during glucosinolate degradation in soil.

Authors:  P D Brown; M J Morra; J P McCaffrey; D L Auld; L Williams
Journal:  J Chem Ecol       Date:  1991-10       Impact factor: 2.626

3.  Isothiocyanates as alleopathic compounds fromRorippa indica Hiern. (Cruciferae) roots.

Authors:  A Yamane; J Fujikura; H Ogawa; J Mizutani
Journal:  J Chem Ecol       Date:  1992-11       Impact factor: 2.626
  3 in total
  2 in total

1.  Isolation and identification of (3-methoxyphenyl)acetonitrile as a phytotoxin from meadowfoam (Limnanthes alba) seedmeal.

Authors:  S F Vaughn; R A Boydston; C A Mallory-Smith
Journal:  J Chem Ecol       Date:  1996-10       Impact factor: 2.626

2.  Induction of Apoptosis and Cytotoxicity by Isothiocyanate Sulforaphene in Human Hepatocarcinoma HepG2 Cells.

Authors:  Saie Brindha Kntayya; Muhammad Din Ibrahim; Nooraini Mohd Ain; Renato Iori; Costas Ioannides; Ahmad Faizal Abdull Razis
Journal:  Nutrients       Date:  2018-06-04       Impact factor: 5.717
  2 in total

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