dc.creatorChinchilla, Nuria
dc.creatorOliveros Bastidas, Alberto
dc.creatorMacías, Francisco A.
dc.creatorMarín, David
dc.creatorMolinillo G., José
dc.creatorVarela, Rosa E.
dc.date2005-07-27
dc.date2005-07-27T09:00:00Z
dc.date2005-07-27T09:00:00Z
dc.date2005-03-01
dc.date2005-07-27T09:00:00Z
dc.date.accessioned2017-03-03T13:51:16Z
dc.date.available2017-03-03T13:51:16Z
dc.identifierT016300002004/0
dc.identifierhttp://www.saber.ula.ve/handle/123456789/16815
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/200925
dc.descriptionStructure-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 Chemistry
dc.descriptionaloliver@ula.ve
dc.descriptionfamacias@uca.es
dc.descriptionNivel monográfico
dc.format294492
dc.languagees
dc.publisherSABER ULA
dc.subjectGrupo de Química Ecológica
dc.subjectEscuela de Ciencias.
dc.subjectFacultad de Ciencias.
dc.subjectDepartamento de Química
dc.subjectRice
dc.subjectEchinochloa crus-galli
dc.subjectBarnyardgrass
dc.subjectBenzoxazinones
dc.subjectDIMBOA
dc.subjectDIBOA
dc.subjectBioassay
dc.subject4-hydroxy-(2 H)-1,4-benzoxazin-3(4 H)-one
dc.subjectPhytotoxicity
dc.subjectArtículos
dc.titleStructure-Activity Relationship Studies of Benzoxazinones and Related Compounds. Phytotoxicity on Echinochloa crus-galli (L.) P. Beauv.


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