Please use this identifier to cite or link to this item: http://hdl.handle.net/1843/SFSA-8GASDU
Type: Tese de Doutorado
Title: Estudo do epicarpo e do mesocarpo externo do fruto de Caryocar brasiliense Camb. (pequi): síntese e biotransformação de isocariolanos e derivados para avaliação da atividade biológica
Authors: Jociani Ascari
First Advisor: Maria Amelia Diamantino Boaventura
First Co-advisor: Jacqueline Aparecida Takahashi
First Referee: Laurent Frederic Gil
Second Referee: Joao Maximo de Siqueira
Third Referee: Lucienir Pains Duarte
metadata.dc.contributor.referee4: Dorila Pilo Veloso
Abstract: O presente trabalho consta de duas partes. Na Parte 1 é descrito o estudo fitoquímico do mesocarpo e epicarpo externo do pequi (Caryocar brasiliense Camb.), sendo a primeira vez que esta parte da planta é estudada. Foram isoladas seis substâncias puras, sendo elas, galato de etila, -hidroximetilfurfural, ácido gálico, chiquimato de metila, galato de metila e quatro misturas, ß-D-frutopiranose e ß-D-frutofuranose, a- e ß-D-glicose, lupeol e ácido oléico, ß-sitosterol e estigmasterol, contaminados com o ácido oléico. Foram avaliadas as atividades citotóxica, antioxidante, alelopática e antimicrobiana sobre o extrato bruto, frações e substâncias puras. Na Parte 2 desta tese foram feitas transformações químicas e biotransformações (pela utilização do fungo B. cinerea) de isocariolanos. Foram isolados 11 produtos de transformação química, sendo eles, 5a-hidroxicariofila- 4(12),8(13)-dieno, (8R,9R)-8-metoxi-isocariolan-9-ol, isocariolan-9-ona,(1S,2S, 5R,8S)-1,4,4-trimetiltriciclo[6.2.1.02, 5]undecano-8-carbaldeído,(8R,9R)-isocariolano -8,9-diol, isocariolan-9a-ol, (1R,2S,5R,8S)-8-hidroximetil-1,4,4-trimetil triciclo[6.2.1.02,5]undecano, (8R,9R)-8-etoxi-isocariolan-9-ol, (8R,9R)-8-propoxiisocariolan- 9-ol, (8R,9R)-8-butoxi-isocariolan-9-ol, (8R,9R)-8-pentoxi-isocariolan-9- ol e 13 novos produtos de biotransformação, sendo eles, (4R,8R,9R)-8-metoxiisocariolan- 9,15-diol, (3S,8R,9R)-isocariolan-3,8,9-triol, (4R,8R,9R)-isocariolan- 8,9,15-triol, (6R,8S,9R)-isocariolan-6,8,9-triol, (2R,5S,8R,9R)-isocariolan-5,8,9- triol, (6S,8S,9R)-isocariolan-6,8,9-triol, (2S,4R,5R)-4-hidroximetil-1,4-dimetiltriciclo [6.3.1.02,5]dodecan-9-ona, (15R,9R)-isocariolan-9,15-diol, (3S,9R)-isocariolan-9,3- diol, (1S,2S,5R,6S,8S)-1-metil-4,4,8-trimetilentriciclo[6.2.1.02,5]undeca-6ß,12-diol, (1R,2S,5R,6S,8R,9S)-1-metil-4,4,8-trimetilentriciclo [6.2.1.02,5]undeca-6ß,9ß,12- triol,(1R,2S,4R,5R,6S,8S)-1-metil-4,4,8- trimetilentriciclo [6.2.1.02,5]undeca-6ß,15,12 -triol, (1S,2S,5R,8S)-1-metil-4,4,8-trimetilentriciclo[6.2.1.02,5]undeca-12,14,15-triol. Foram realizados testes de avaliação das atividades fungistática e alelopática sobre alguns dos derivados isocariolânicos isolados.
Abstract: This Thesis consists of two parts. In Part 1, the phytochemical study of mesocarpe and external epicarpe of pequi (Caryocar brasiliense Camb.) and their biological activity are described. This study led to the isolation of six pure compounds, ethyl gallate, 5-hydroxymethylfurfural, gallic acid, methyl shikimate, methyl gallate and four mixtures, -D-fructopiranose and -D-fructofuranose, - and -D-glucose, lupeol and oleic acid, -sitosterol and stigmasterol, contaminated with oleic acid. Biological assays for citotoxic, antioxidant, antimicrobial and allelopathicactivities were carried out for the crude extract, fractions and pure substances. In Part 2 of this thesis we describe chemical transformations and biotransformations (by using the fungus B. cinerea) of isocariolane compounds, resulting in 11 new products of chemical transformations, 5-hidroxycaryophylla-4(12),8(13)-diene, (8R,9R)-8-methoxyisocariolan-9-ol, isocaryolan-9-one,(1S,2S,5R,8S)-1,4,4-trimetyltriciclo[6.2.1.02,5] undecane-8-carbaldehyde, (8R,9R)- isocaryolan-8,9-diol, isocaryolan-9-ol, (1R,2S,5R,8S)-8-hydroxymethyl-1,4,4- trimethyltricicle[6.2.1.02,5]undecan, (8R,9R)-8-etoxyisocariolan -9-ol, (8R,9R)-8- propoxyisocariolan-9-ol, (8R,9R)-8-butoxyisocariolan-9-ol, (8R,9R)-8- pentoxyisocariolan-9-ol and 13 new biotransformation products, (4R,8R,9R)-8-metoxyisocariolan-9,15-diol, (3S,8R,9R)-isocaryolan-3,8,9-triol, (4R,8R,9R)- isocaryolan-8,9,15-triol, (6R,8S,9R)-isocaryolan-6,8,9-triol, (2R,5S, 8R,9R)- isocaryolan-5,8,9-triol, (6S,8S,9R)-isocaryolan-6,8,9-triol, (2S,4R,5R)-4- hydroxymethyl-1,4-dimethyltricycle[6.3.1.02,5]dodecan-9-one, (15R,9R)-isocaryolan-9,15-diol, (3S,9R)- isocaryolan-9,3-diol, (1S,2S,5R,6S,8S)-1-methyl- 4,4,8-trimethylentricycle[6.2.1.02,5]undeca-6,12-diol, (1R,2S,5R,6S,8R,9S)-1- methyl-4,4,8-trimethylentricycle[6.2.1.02,5]undeca-6,9,12-triol, (1R,2S,4R,5R,6S, 8S)-1-methyl-4,4,8-trimethylentricycle[6.2.1.02,5]undeca-6,15,12-triol, (1S,2S,5R,8S)-1-methyl-4,4,8-trimethylentricycle[6.2.1.02,5]undeca-12,14,15-triol .Bioassays to evaluate fungistatic and allelophatic activities of someisoariolanes isolated were carried out.
Subject: Química orgânica
Caqui
Caryocar
Química
Biotransformação (Metabolismo)
language: Português
Publisher: Universidade Federal de Minas Gerais
Publisher Initials: UFMG
Rights: Acesso Aberto
URI: http://hdl.handle.net/1843/SFSA-8GASDU
Issue Date: 29-Mar-2011
Appears in Collections:Teses de Doutorado

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