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1.
J Agric Food Chem ; 71(47): 18227-18238, 2023 Nov 29.
Artigo em Inglês | MEDLINE | ID: mdl-37567224

RESUMO

Herbicides are effective tools to manage weeds and enable food production and sustainable agriculture. Corteva Agriscience R&D has recently discovered new diphenyl-ether compounds displaying excellent postemergent efficacy on important weed species along with corn safety. Here, we describe the chemistry, biology, biochemistry, and computational modeling research that led to the discovery and elucidation of the primary mode of action for these compounds. The target protein was found to be acetolactate synthase (ALS), a key enzyme in the biosynthesis of branched chain amino acids (valine, leucine, and isoleucine). While weed resistance evolution to ALS herbicides is widespread, the molecular interaction of the diphenyl-ether compounds at the active site of the ALS enzyme differs significantly from that of some commercial ALS inhibitors. The unique biochemical profile of these molecules along with their excellent herbicidal activity and corn selectivity make them a noteworthy development in the pursuit of novel, safe, and sustainable weed control solutions.


Assuntos
Acetolactato Sintase , Herbicidas , Herbicidas/farmacologia , Herbicidas/química , Acetolactato Sintase/química , Resistência a Herbicidas , Éteres
2.
J Agric Food Chem ; 71(47): 18171-18187, 2023 Nov 29.
Artigo em Inglês | MEDLINE | ID: mdl-37350671

RESUMO

We report on the development of a novel class of diaryl ether herbicides. After the discovery of a phenoxybenzoic acid with modest herbicidal activity, optimization led to several molecules with improved control of broadleaf and grass weeds. To facilitate this process, we first employed a three-step combinatorial approach, then pivoted to a one-step Ullmann-type coupling that provided faster access to new analogs. After determining that the primary target site of our benchmark diaryl ethers was acetolactate synthase (ALS), we further leveraged this copper-catalyzed methodology to conduct a scaffold hopping campaign in the hope of uncovering an additional mode of action with fewer documented cases of resistance. Our comprehensive and systematic investigation revealed that while the herbicidal activity of this area seems to be exclusively linked to ALS inhibition, our molecules represent a structurally distinct class of Group 2 herbicides. The structure-activity relationships that led us to this conclusion are described herein.


Assuntos
Acetolactato Sintase , Herbicidas , Herbicidas/farmacologia , Éter , Relação Estrutura-Atividade , Éteres/farmacologia , Plantas Daninhas/metabolismo , Etil-Éteres , Acetolactato Sintase/metabolismo , Resistência a Herbicidas
3.
Bioorg Med Chem ; 24(3): 362-71, 2016 Feb 01.
Artigo em Inglês | MEDLINE | ID: mdl-26321602

RESUMO

Multiple classes of commercially important auxin herbicides have been discovered since the 1940s including the aryloxyacetates (2,4-D, MCPA, dichlorprop, mecoprop, triclopyr, and fluroxypyr), the benzoates (dicamba), the quinoline-2-carboxylates (quinclorac and quinmerac), the pyrimidine-4-carboxylates (aminocyclopyrachlor), and the pyridine-2-carboxylates (picloram, clopyralid, and aminopyralid). In the last 10 years, two novel pyridine-2-carboxylate (or picolinate) herbicides were discovered at Dow AgroSciences. This paper will describe the structure activity relationship study that led to the discovery of the 6-aryl-picolinate herbicides Arylex™ active (2005) and Rinskor™ active (2010). While Arylex was developed primarily for use in cereal crops and Rinskor is still in development primarily for use in rice crops, both herbicides will also be utilized in additional crops.


Assuntos
Descoberta de Drogas , Grão Comestível/efeitos dos fármacos , Herbicidas/farmacologia , Ácidos Indolacéticos/farmacologia , Oryza/efeitos dos fármacos , Picloram/análogos & derivados , Herbicidas/síntese química , Herbicidas/química , Ácidos Indolacéticos/síntese química , Ácidos Indolacéticos/química , Picloram/síntese química , Picloram/química , Picloram/farmacologia , Relação Estrutura-Atividade
4.
Pest Manag Sci ; 58(12): 1175-86, 2002 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-12476990

RESUMO

A novel series of substituted 3-phenyl benzoylpyrazoles were prepared and tested as potential grass herbicides. The targeted materials were prepared by three newly developed synthetic routes, which allowed a comprehensive study of the SAR (structure-activity relationships) of this series. The best combination of grass weed activity (Avena fatua L, Setaria viridis (L) Beauv and Alopecurus myosuroides Huds) and wheat selectivity was obtained with an alkoxy group in the 4-position of the phenyl ring. Activity was further enhanced by the presence of tert-butyl on the pyrazole and a methyl group at the C-2 position of the benzoyl moiety. The alkoxy-substituted 3-phenylbenzoylpyrazoles are a novel class of herbicides with potential utility for control of important grass weeds in cereals.


Assuntos
Herbicidas/toxicidade , Pirazóis/toxicidade , 4-Hidroxifenilpiruvato Dioxigenase/antagonistas & inibidores , Herbicidas/síntese química , Espectroscopia de Ressonância Magnética , Estrutura Molecular , Poaceae/efeitos dos fármacos , Pirazóis/síntese química , Relação Estrutura-Atividade
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