1.Isolation and characterization of xanthine oxidase inhibitory constituents of Pyrenacantha staudtii
Abiodun FALODUN ; Muhammad Irfan QADIR ; Muhanmad Iqbal CHOULDARY
Acta Pharmaceutica Sinica 2009;44(4):390-394
Six compounds have been isolated from the leaves of Pyrenacantha staudtii,two of which are new compounds.The new compounds have been characterized as kaempherol 3-O-β-rhamnopyranosyl (1→6)β-D-glucopyranoside (1) and 4-β-glucopyranosyl-(2-furyl)-5-methy-1,2-glucopyranoside phenylmethanone (2).The known compounds are 3-pyridinecarboxylic acid (3),β-sitosterol (4),sitosterol 3-O-β-glucopyranoside (5) and taraxerol (6).Their structures were determined by spectroscopic and chemical evidences.The two new compounds together with 3-pyridinecarboxylic acid showed significant in vitro xanthine oxidase inhibitory activity.To the best of our knowledge,this is the first report of these compounds from this plant.
2.Isolation and characterization of xanthine oxidase inhibitory constituents of Pyrenacantha staudtii.
Abiodun FALODUN ; Muhammad Irfan QADIR ; Muhammad Iqbal CHOULDARY
Acta Pharmaceutica Sinica 2009;44(4):390-394
Six compounds have been isolated from the leaves of Pyrenacantha staudtii, two of which are new compounds. The new compounds have been characterized as kaempherol 3-O-beta-rhamnopyranosyl (1-->6)-beta-D-glucopyranoside (1) and 4-beta-glucopyranosyl-(2-furyl)-5-methy-1,2-glucopyranoside phenylmethanone (2). The known compounds are 3-pyridinecarboxylic acid (3), beta-sitosterol (4), sitosterol 3-O-beta-glucopyranoside (5) and taraxerol (6). Their structures were determined by spectroscopic and chemical evidences. The two new compounds together with 3-pyridinecarboxylic acid showed significant in vitro xanthine oxidase inhibitory activity. To the best of our knowledge, this is the first report of these compounds from this plant.
Enzyme Inhibitors
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chemistry
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isolation & purification
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pharmacology
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Glucosides
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chemistry
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isolation & purification
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pharmacology
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Kaempferols
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chemistry
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isolation & purification
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pharmacology
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Magnoliopsida
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chemistry
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Molecular Structure
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Niacin
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chemistry
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isolation & purification
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pharmacology
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Plant Leaves
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chemistry
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Plants, Medicinal
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chemistry
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Xanthine Oxidase
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metabolism
3. Isolation of antileishmanial, antimalarial and antimicrobial metabolites from Jatropha multifida
Abiodun FALODUN ; Vincent IMIEJE ; Osayewenre ERHARUYI ; Ahomafor JOY ; Abiodun FALODUN ; Mohammed ABALDRY ; Mark HAMANN ; Vincent IMIEJE ; Osayewenre ERHARUYI ; Peter LANGER ; Melissa JACOB ; Shabanna KHAN
Asian Pacific Journal of Tropical Biomedicine 2014;4(5):374-378
Objective: To investigate the antileishmanial, antimicrobial and antimalarial activities of the pure metabolites from Jatropha multifida used in African ethnomedicine. Methods: The methanolic stem bark extract of Jatropha multifida used in Nigerian folk medicine as remedy against bacterial infections was subjected to column chromatography and HPLC analyses to obtain three known metabolites, microcyclic lathyrane diterpenoids (1-3). Structures were confirmed by comparison of 1D and 2D spectral data with literature. Results: The three compounds exhibited inhibition of antileishmanial, antimalarial and antimicrobial actions against the tested organisms with compouds 2 and 3 active against Cryptococcus neoformans at IC
4.Isolation of antileishmanial, antimalarial and antimicrobial metabolites from Jatropha multifida.
Abiodun FALODUN ; Vincent IMIEJE ; Osayewenre ERHARUYI ; Ahomafor JOY ; Peter LANGER ; Melissa JACOB ; Shabanna KHAN ; Mohammed ABALDRY ; Mark HAMANN
Asian Pacific Journal of Tropical Biomedicine 2014;4(5):374-378
OBJECTIVETo investigate the antileishmanial, antimicrobial and antimalarial activities of the pure metabolites from Jatropha multifida used in African ethnomedicine.
METHODSThe methanolic stem bark extract of Jatropha multifida used in Nigerian folk medicine as remedy against bacterial infections was subjected to column chromatography and HPLC analyses to obtain three known metabolites, microcyclic lathyrane diterpenoids (1-3). Structures were confirmed by comparison of 1D and 2D spectral data with literature.
RESULTSThe three compounds exhibited inhibition of antileishmanial, antimalarial and antimicrobial actions against the tested organisms with compouds 2 and 3 active against Cryptococcus neoformans at IC50 of 8.2 and 8.7 µg/mL, respectively.
CONCLUSIONSThe research lends support to the ethnomedicinal use of the plant in combating microbial infections, leishmaniasis and malarial infections.