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dc.contributor.authorHORTA, L. P.pt_BR
dc.contributor.authorMOTTA, Y. C. C.pt_BR
dc.contributor.authorBARBOSA, G. M.pt_BR
dc.contributor.authorBRAGA, T. C.pt_BR
dc.contributor.authorMARRIEL, I. E.pt_BR
dc.contributor.authorFÁTIMA, A. dept_BR
dc.contributor.authorMODOLO, L. V.pt_BR
dc.date.accessioned2017-06-08T00:21:26Z-
dc.date.available2017-06-08T00:21:26Z-
dc.date.created2016-08-09pt_BR
dc.date.issued2016pt_BR
dc.identifier.citationJournal of the Brazilian Chemical Society, São Paulo, v. 27, n. 8, p. 1512-1519, 2016.pt_BR
dc.identifier.urihttp://www.alice.cnptia.embrapa.br/alice/handle/doc/1050539pt_BR
dc.descriptionThe plant phenolic natural products (PNPs) protocatechuic aldehyde, syringaldehyde and vanillin were used as platforms for obtaining four urease inhibitors. Urea (urease substrate) or thiourea (urease inhibitor) core was added to the structure of newly synthesized compounds to provide inhibitors up to 230-fold more active than the PNPs they originated from. The PNP derivatives are mixed inhibitors with higher affinity to urease active site. Two compounds were as efficient as N-(butyl)thiophosphoric triamide (NBPT) toward soil. Overall, PNPs derivatives are promising urease inhibitors for use as additive in urea-based fertilizers formulations.pt_BR
dc.language.isoengeng
dc.rightsopenAccesseng
dc.titleUrease inhibitors of agricultural interest inspired by structures of plant phenolic aldehydes.pt_BR
dc.typeArtigo de periódicopt_BR
dc.date.updated2017-06-08T00:21:26Zpt_BR
dc.subject.nalthesaurusureapt_BR
riaa.ainfo.id1050539pt_BR
riaa.ainfo.lastupdate2017-06-07pt_BR
dc.identifier.doi10.21577/0103-5053.20160208pt_BR
dc.contributor.institutionIVANILDO EVODIO MARRIEL, CNPMS.pt_BR
Aparece en las colecciones:Artigo em periódico indexado (CNPMS)

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