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dc.creatorAlmeida, Mauro Vieira de-
dc.creatorSilva, Adilson David da-
dc.creatorSouza, Marcus Vinícius Nora de-
dc.creatorBenício, Aloísio Antônio Alves-
dc.date.accessioned2019-02-22T12:20:38Z-
dc.date.available2019-02-19-
dc.date.available2019-02-22T12:20:38Z-
dc.date.issued2003-02-
dc.citation.volume26pt_BR
dc.citation.issue1pt_BR
dc.citation.spage105pt_BR
dc.citation.epage111pt_BR
dc.identifier.doihttp://dx.doi.org/10.1590/S0100-40422003000100018pt_BR
dc.identifier.urihttps://repositorio.ufjf.br/jspui/handle/ufjf/9118-
dc.description.abstractInositol is a polyalcohol required for the proper formation of cell membranes. In the body, its plays an important role in the transmission of nerve impulses, its also helps in the transporting of fats within the body. In mammals, inositol exists as phosphorylated derivatives, various phosphoinositides, and in its free form. Agonist stimulated hydrolysis of phosphatidylinositol 4,5-bisphosphate [PI(4,5)P2] is the first step in the transmembrane signalling mechanism when cells respond to external stimuli. Under control of activated phospholipase C (PLC) via G-protein, two second messengers D-myo-inositol 1,4,5-triphosphate [Ins(1,4,5)P3] and diacylglycerol are released into the cell. From Ins(1,4,5)P3, enzymatic process under phosphatases or kinases control affords subsequent inositol phosphate metabolites. During the last decade the synthesis of modified inositol phosphate derivatives has been strongly investigated. This paper reviews principal aspects about synthesis and biological functions of these biomolecules.pt_BR
dc.description.resumo-pt_BR
dc.languageporpt_BR
dc.publisher-pt_BR
dc.publisher.countryBrasilpt_BR
dc.publisher.initials-pt_BR
dc.relation.ispartofQuímica Novapt_BR
dc.rightsAcesso Abertopt_BR
dc.subjectSecond messengerspt_BR
dc.subjectPhosphoinositidespt_BR
dc.subjectInositol phosphatept_BR
dc.subject.cnpq-pt_BR
dc.titleA cascata dos fosfoinositídeospt_BR
dc.title.alternativeThe phosphoinositide cascatept_BR
dc.typeArtigo de Periódicopt_BR
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