References of "Angenot, Luc"
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See detailA propos des remèdes végétaux à visée amaigrissante
Angenot, Luc ULg

Article for general public (2001)

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See detailAllocution du 8.9.2001 Promotion 2001 (Avenir du métier de pharmacien)
Angenot, Luc ULg

Speech/Talk (2001)

Résultats de la promotion et considérations sur l'avenir du métier de pharmacien à l'aube du 3e millénaire

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See detailReversal of Chloroquine and Mefloquine Resistance in Plasmodium Falciparum by the Two Monoindole Alkaloids, Icajine and Isoretuline
Frederich, Michel ULg; Hayette, Marie-Pierre ULg; Tits, Monique ULg et al

in Planta Medica (2001), 67(6), 523-7

Eight naturally occurring monoindole alkaloids were evaluated in vitro for their ability to inhibit Plasmodium falciparum growth and, in drug combination, to reverse the resistance of a chloroquine ... [more ▼]

Eight naturally occurring monoindole alkaloids were evaluated in vitro for their ability to inhibit Plasmodium falciparum growth and, in drug combination, to reverse the resistance of a chloroquine-resistant strain of Plasmodium falciparum. None of these indole alkaloids has significant intrinsic antiplasmodial activity (IC(50) > 10 microM or 5 microg/ml). Nevertheless, three alkaloids (icajine, isoretuline and strychnobrasiline) did reverse chloroquine resistance at concentrations between 2.5 and 25 microg/ml (IF of 12.82 for isoretuline on W2 strain). The Interaction Factor (IF) equals 2, < 2, or > 2 for additive, antagonistic or synergistic effects of alkaloids on chloroquine inhibition, respectively. Icajine and isoretuline were also assessed in vitro for their mefloquine potentiating activity on a mefloquine-resistant strain of Plasmodium falciparum. Only icajine proved to be synergistic with mefloquine (IF = 15.38). [less ▲]

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See detailMain Glucosidase Conversion Products of the Gluco-Alkaloids Dolichantoside and Palicoside
Brandt, V.; Tits, Monique ULg; Penelle, J. et al

in Phytochemistry (2001), 57(5), 653-9

The enzymatic glucose cleavage of palicoside revealed the biosynthetic pathway to akagerine, whereas the conversion of dolichantoside led to a new quaternary heteroyohimbine alkaloid named N(b)-methyl-21 ... [more ▼]

The enzymatic glucose cleavage of palicoside revealed the biosynthetic pathway to akagerine, whereas the conversion of dolichantoside led to a new quaternary heteroyohimbine alkaloid named N(b)-methyl-21-beta-hydroxy-mayumbine. The hypothetical models of reactions occurring after the conversion of both substrates are proposed. Dolichantoside and palicoside, as well as Strychnos mellodora stem bark crude ethanol extract, exhibit significant antimycotic activity against human pathogens in presence of specific glucosidase. [less ▲]

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See detailStrychnogucines a and B, Two New Antiplasmodial Bisindole Alkaloids from Strychnos Icaja
Frederich, Michel ULg; De Pauw-Gillet, Marie-Claire ULg; Prosperi, Christelle ULg et al

in Journal of Natural Products (2001), 64(1), 12-16

A reinvestigation of Strychnos icaja roots has resulted in the isolation of two tertiary quasi-symmetric bisindole alkaloids named strychnogucines A (1) and B (2). Their structures were identified by ... [more ▼]

A reinvestigation of Strychnos icaja roots has resulted in the isolation of two tertiary quasi-symmetric bisindole alkaloids named strychnogucines A (1) and B (2). Their structures were identified by means of spectroscopic data interpretation. Compound 2 was highly active in vitro and compound 1 moderately active against four strains of Plasmodium falciparum. Strychnogucine B (2) was more active against a chloroquine-resistant strain than against a chloroquine-sensitive one (best CI(50), 80 nM against the W2 strain). In addition, this compound showed a selective antiplasmodial activity with 25-180 times greater toxicity toward P. falciparum, relative to cultured human cancer cells (KB) or human fibroblasts (WI38). [less ▲]

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See detailCriterii de differentiere a unor specii de Veronica
Crisan, Gianina; Tamas, M.; Garbacki, Nancy ULg et al

in Farmacia (2001), 49(6), 67-73

We have tried to establish some criteria to avoid the substitution of Veronica officinalis L; with anti-ulcer and anti-inflammatory activities with other species of the genus Veronica, especially Veronica ... [more ▼]

We have tried to establish some criteria to avoid the substitution of Veronica officinalis L; with anti-ulcer and anti-inflammatory activities with other species of the genus Veronica, especially Veronica chamaedrys L. widely spread and without therapeutic use. We have studied the different histological, anatomical and phytochemical characters for the two species. A rapid method for the identification of both species is the TLC for flavonoids and phenylpropanic compounds was described. Moreover HPLC is useful to detect the presence of acteoside only in Veronica chamaedrys, while Veronica officinalis contains isoacteoside. [less ▲]

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See detailAnti-inflammatory effects of Centaurea cyanus (Asteraceae) flower-heads.
Garbacki, Nancy ULg; Gloaguen, Vincent; Damas, Jacques ULg et al

Poster (2001)

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See detailStrychnogucines A and B, two new antiplasmodial bisindole alkaloids from Strychnos icaja
Frederich, Michel ULg; Tits, Monique ULg; Penelle, Jacques et al

Poster (2000, September)

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See detailVeronica officinalis L. et Veronica chamaedrys L.: étude des différences morphologiques et phytochimiques
Crisan, Gianina; Tamas, Mircea; Garbacki, Nancy ULg et al

Poster (2000, July)

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See detailAntiinflammatory and chonroprotective activity of prodelphinidins isolated from Ribes nigrum leaves
Tits, Monique ULg; de Leval Xavier; Dierckxsens, Yvan et al

Poster (2000, July)

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See detailNouvelle méthode d'extraction et d'isolement de l'isostrychnopentamine à partir des feuilles de Strychnos usambarensis
Cristino, Assunçao; Tits, Monique ULg; Penelle, Jacques et al

Poster (2000, July)

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See detailPalicoside: précurseur naturel de l'akagérine
Brandt, Viviane; Tits, Monique ULg; Penelle, Jacques et al

Poster (2000, July)

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