Fractionation, isolation, and characterization of some Amorphophallus sp, secondary metabolites

The crude alcoholic extracts of stems and leaves as well as tubers and roots were fractionated by sequential extraction. Extracts obtained from this step were set aside for physiological activity testing. The hexane extract of tubers and roots was chosen for further fractionation based on their TLC...

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Main Authors: Mendoza, Edna Patricia P., Nidea, Marianne Joy S.
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語言:English
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語言: English
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spelling oai:animorepository.dlsu.edu.ph:etd_bachelors-65312021-07-12T06:02:56Z Fractionation, isolation, and characterization of some Amorphophallus sp, secondary metabolites Mendoza, Edna Patricia P. Nidea, Marianne Joy S. The crude alcoholic extracts of stems and leaves as well as tubers and roots were fractionated by sequential extraction. Extracts obtained from this step were set aside for physiological activity testing. The hexane extract of tubers and roots was chosen for further fractionation based on their TLC profile. This extract was fractionated by column chromatography with the aim of getting some pure actions. The Amorphophallus sp. is a well-known remedial plant for a number of ailments, but reports on the secondary metabolites of Amorphophallus sp. are limited. With the limited reports, there remains a need to bridge the gap between the identified metabolites of these plants and their actual psychological activities. This study partially addressed both concerns. Thirty-six (36) fractions were obtained from column chromatography. The major non-polar band (Fractions 16 & 17) was obtained as a semi-pure fraction (ACT 1-16). This was not purified further but was analyzed by GC-Ms. Ergosta-5, 22-dien-3-ol, acetate (RT 24.64 min), lupeol (RT 24.65 min), betulin (RT 24.70 min), 3-aceto-12-hydroxyoleanane (RT 24.76 min), and 3-aceto-20-hydroxy-12-taraxastene (RT 34.24 min) were identified from the GC-MS data of this fraction. A second band composed of fractions 32 to 36 appeared to be with while flaky crystals. The combined fractions (ACT1-36). The white crystals obtained from the recrystallization over methanol. The spectral data analysis of this compound revealed a high molecular weight compound (m/z 1700). The NMR data showed mainly solvent peaks. The sample was dissolved in CDCl3, which did not dissolve the sample. The rest of the fractions were set aside for activity testing. 2005-01-01T08:00:00Z text https://animorepository.dlsu.edu.ph/etd_bachelors/5887 Bachelor's Theses English Animo Repository Amorphophallus Amorphous substances Metabolites
institution De La Salle University
building De La Salle University Library
continent Asia
country Philippines
Philippines
content_provider De La Salle University Library
collection DLSU Institutional Repository
language English
topic Amorphophallus
Amorphous substances
Metabolites
spellingShingle Amorphophallus
Amorphous substances
Metabolites
Mendoza, Edna Patricia P.
Nidea, Marianne Joy S.
Fractionation, isolation, and characterization of some Amorphophallus sp, secondary metabolites
description The crude alcoholic extracts of stems and leaves as well as tubers and roots were fractionated by sequential extraction. Extracts obtained from this step were set aside for physiological activity testing. The hexane extract of tubers and roots was chosen for further fractionation based on their TLC profile. This extract was fractionated by column chromatography with the aim of getting some pure actions. The Amorphophallus sp. is a well-known remedial plant for a number of ailments, but reports on the secondary metabolites of Amorphophallus sp. are limited. With the limited reports, there remains a need to bridge the gap between the identified metabolites of these plants and their actual psychological activities. This study partially addressed both concerns. Thirty-six (36) fractions were obtained from column chromatography. The major non-polar band (Fractions 16 & 17) was obtained as a semi-pure fraction (ACT 1-16). This was not purified further but was analyzed by GC-Ms. Ergosta-5, 22-dien-3-ol, acetate (RT 24.64 min), lupeol (RT 24.65 min), betulin (RT 24.70 min), 3-aceto-12-hydroxyoleanane (RT 24.76 min), and 3-aceto-20-hydroxy-12-taraxastene (RT 34.24 min) were identified from the GC-MS data of this fraction. A second band composed of fractions 32 to 36 appeared to be with while flaky crystals. The combined fractions (ACT1-36). The white crystals obtained from the recrystallization over methanol. The spectral data analysis of this compound revealed a high molecular weight compound (m/z 1700). The NMR data showed mainly solvent peaks. The sample was dissolved in CDCl3, which did not dissolve the sample. The rest of the fractions were set aside for activity testing.
format text
author Mendoza, Edna Patricia P.
Nidea, Marianne Joy S.
author_facet Mendoza, Edna Patricia P.
Nidea, Marianne Joy S.
author_sort Mendoza, Edna Patricia P.
title Fractionation, isolation, and characterization of some Amorphophallus sp, secondary metabolites
title_short Fractionation, isolation, and characterization of some Amorphophallus sp, secondary metabolites
title_full Fractionation, isolation, and characterization of some Amorphophallus sp, secondary metabolites
title_fullStr Fractionation, isolation, and characterization of some Amorphophallus sp, secondary metabolites
title_full_unstemmed Fractionation, isolation, and characterization of some Amorphophallus sp, secondary metabolites
title_sort fractionation, isolation, and characterization of some amorphophallus sp, secondary metabolites
publisher Animo Repository
publishDate 2005
url https://animorepository.dlsu.edu.ph/etd_bachelors/5887
_version_ 1712576506015776768