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dc.rights.licensehttp://creativecommons.org/licenses/by-nc-sa/3.0/ve/
dc.contributor.authorChinchilla, Nuriaes_VE
dc.contributor.authorOliveros Bastidas, Albertoes_VE
dc.contributor.authorMacías, Francisco A.es_VE
dc.contributor.authorMarín, Davides_VE
dc.contributor.authorMolinillo G., Josées_VE
dc.contributor.authorVarela, Rosa E.es_VE
dc.date2005-07-27es_VE
dc.date.accessioned2005-07-27T09:00:00Z
dc.date.available2005-07-27T09:00:00Z
dc.date.created2005-03-01es_VE
dc.date.issued2005-07-27T09:00:00Zes_VE
dc.identifier.otherT016300002004/0es_VE
dc.identifier.urihttp://www.saber.ula.ve/handle/123456789/16815
dc.description.abstractStructure-Activity Relationship Studies of Benzoxazinones and Related Compounds. Phytotoxicity on Echinochloa crus-galli (L.) P. Beauv (Macías, Francisco A.; Chinchilla, Nuria; Varela, Rosa M.; Oliveros, Alberto; Marín, David; and Molinillo G., José M.) Abstract Echinochloa crus-galli ( E. crus-galli; barnyardgrass) is a weed widely distributed. It constitutes a serious weed problem in 42 countries and has been found in at least 27 more. It is the world's main weed of rice affecting up to 36 crops worldwide. Several biotypes of this plant, with resistance to herbicides with different modes of action have evolved. In our ongoing studies regarding the potential application of benzoxazinones and their soil degradation products for weed control, a complete structure-activity relationships (SARs) study was made by using barnyardgrass as the target plant. Compounds used in this study were previously tested on a wide variety of standard target species (STS), and they include natural allelochemicals 2- O-â-D-glucopyranosyl-4-hydroxy-(2 H)-1,4-benzoxazin-3(4 H)-one (DIBOA-Glc), 2,4-dihydroxy-7-methoxy-(2H)-1,4-benzoxazin-3(4H)-one (DIMBOA), and 2,4-dihydroxy- (2 H)-1,4-benzoxazin-3(4 H)-one (DIBOA), together with some degradation derivatives found in wheat crop soil and some synthetic analogues. Their phytotoxicity on E. crus-galliis discussed and compared with the results obtained from previous screening. This work constitutes the next step in the search for natural herbicide models based on benzoxazinones and their degradation products. The most active compounds were the degradation product 2-aminophenol (APH) and the synthetic analogue 4-hydroxy-(2 H)-1,4-benzoxazin-3(4 H)-one (D-DIBOA). Their activities confirm the direction proposed in our previous SAR study, which establishes D-DIBOA to be the best lead for natural herbicide model development with benzoxazinone structure. Published on: Journal Agricultural and Food Chemistryes_VE
dc.format.extent294492es_VE
dc.language.isoeses_VE
dc.publisherSABER ULAes_VE
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectGrupo de Química Ecológicaes_VE
dc.titleStructure-Activity Relationship Studies of Benzoxazinones and Related Compounds. Phytotoxicity on Echinochloa crus-galli (L.) P. Beauv.es_VE
dc.typeinfo:eu-repo/semantics/article
dc.description.emailaloliver@ula.vees_VE
dc.description.emailfamacias@uca.eses_VE
dc.description.tiponivelNivel monográficoes_VE
dc.subject.departamentoDepartamento de Químicaes_VE
dc.subject.escuelaEscuela de Ciencias.es_VE
dc.subject.facultadFacultad de Ciencias.es_VE
dc.subject.keywordsRicees_VE
dc.subject.keywordsEchinochloa crus-gallies_VE
dc.subject.keywordsBarnyardgrasses_VE
dc.subject.keywordsBenzoxazinoneses_VE
dc.subject.keywordsDIMBOAes_VE
dc.subject.keywordsDIBOAes_VE
dc.subject.keywordsBioassayes_VE
dc.subject.keywords4-hydroxy-(2 H)-1,4-benzoxazin-3(4 H)-onees_VE
dc.subject.keywordsPhytotoxicityes_VE
dc.subject.tipoArtículoses_VE


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