The in vitro antimalarial activities against Plasmodium falciparum K1 of four extracts from the stembark
of Picrasma javanica Bl; ie water, methanol, chloroform and hexane extracts were studied using a modification
of the [3
H]hypoxanthine incorporation method. It was found that the hexane extract showed in vitro antimalarial
activity with IC50 of 3.3 μg/ml. The extract was further fractionated using quick column chromatography, resulting
in ten fractions. Fraction V was the most effective against P. falciparum K1 with IC50 of 4.4 μg/ml. Further
isolation of fraction V using a column chromatographic technique provided six fractions. According to 1
H- and 13C-NMR spectra, it could be concluded that the major compound in fraction V-3 was β-sitosterol. Unfortunately,
the antimalarial activity of β-sitosterol could not be determined because of its low solubility in DMSO. However,
fractions V-2 and V-4 still showed in vitro antimalarial activities with IC50 of 2.8 and 3.4 μg/ml, respectively. The
further fractionation of these two active fractions could lead to promising candidates as antimalarial agents.
The in vitro antimalarial activities against Plasmodium falciparum K1 of four extracts from the stembarkof Picrasma javanica Bl; ie water, methanol, chloroform and hexane extracts were studied using a modificationof the [3H]hypoxanthine incorporation method. It was found that the hexane extract showed in vitro antimalarialactivity with IC50 of 3.3 μg/ml. The extract was further fractionated using quick column chromatography, resultingin ten fractions. Fraction V was the most effective against P. falciparum K1 with IC50 of 4.4 μg/ml. Furtherisolation of fraction V using a column chromatographic technique provided six fractions. According to 1H- and 13C-NMR spectra, it could be concluded that the major compound in fraction V-3 was β-sitosterol. Unfortunately,the antimalarial activity of β-sitosterol could not be determined because of its low solubility in DMSO. However,fractions V-2 and V-4 still showed in vitro antimalarial activities with IC50 of 2.8 and 3.4 μg/ml, respectively. Thefurther fractionation of these two active fractions could lead to promising candidates as antimalarial agents.
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The Plasmodium falciparum in vitro antimalarial activities against K1 of Four extracts from the Stembark
of Picrasma javanica Bl; IE Water, methanol, chloroform and hexane extracts were studied using a modification
of the [3
H] Hypoxanthine Incorporation method. It was that the hexane Extract Found in vitro antimalarial Showed
Activity with IC50 of 3.3 g / ml. The Extract was further fractionated using column chromatography quick, resulting
in Ten fractions. Fraction V was the most effective against P. falciparum K1 with IC50 of 4.4 μg / ml. Further
isolation of fraction V using a column chromatographic fractions Six Technique provided. According to 1
H-NMR and 13C-Spectra, it could be concluded that the Major Compound in beta-sitosterol was fraction V-3. Unfortunately,
beta-sitosterol of the antimalarial Activity could not be determined because of its low solubility in DMSO. However,
fractions V-2 and V-4 still Showed in vitro antimalarial activities with IC50 of 2.8 and 3.4 g / ml, respectively. The
further fractionation of these active fractions could Lead to Two Candidates promising as antimalarial agents.
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The in vitro antimalarial activities against Plasmodium falciparum K1 of four extracts from the stembark
of Picrasma javanica. Bl; ie, water methanol chloroform and, hexane extracts were studied using a modification
of the [3
H] hypoxanthine incorporation. Method. It was found that the hexane extract showed in vitro antimalarial
activity with IC50 of 3.3 thermal g / ml.The extract was further fractionated using quick, column chromatography resulting
in ten fractions. Fraction V was the. Most effective against P. Falciparum K1 with IC50 of 4.4 thermal g / ml. Further
isolation of fraction V using a column chromatographic. Technique provided six fractions. According to 1
H - and, 13C-NMR spectraIt could be concluded that the major compound in fraction V-3 was β - sitosterol. Unfortunately
the, antimalarial activity. Of β - sitosterol could not be determined because of its low solubility in DMSO. However
fractions, V-2 and V-4 still showed. In vitro antimalarial activities with IC50 of 2.8 and 3.4 thermal g /, ML respectively. The
.Further fractionation of these two active fractions could lead to promising candidates as antimalarial agents.
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