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Nadine Azas

Researcher at Aix-Marseille University

Publications -  52
Citations -  1439

Nadine Azas is an academic researcher from Aix-Marseille University. The author has contributed to research in topics: Plasmodium falciparum & Quinoxaline. The author has an hindex of 20, co-authored 52 publications receiving 1187 citations. Previous affiliations of Nadine Azas include University of the Mediterranean & Université Paul Cézanne Aix-Marseille III.

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1,3-Diphenylpyrazoles: synthesis and antiparasitic activities of azomethine derivatives

TL;DR: In the most cases, nitrated compounds were found to be more efficient than non-nitrated ones against Plasmodium falciparum, Trichomonas vaginalis and Leishmania infantum.
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Synthesis and antiplasmodial activity of new 4-aryl-2-trichloromethylquinazolines

TL;DR: A series of original 4-aryl-substituted 2-trichloromethylquinazoline derivatives was synthesized using a microwave-assisted Suzuki-Miyaura cross-coupling approach, revealing their antiplasmodial potential.
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Original quinazoline derivatives displaying antiplasmodial properties.

TL;DR: The structure activity relationships establish that the molecular scaffold which exerts the best profile is the 6-nitro-2-(tosylmethyl)-N-(3-substituted-phenyl)-quinazolin-4-amine, showing that these molecules display a selective antiplasmodial activity.
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Phytochemical and pharmacological study of roots and leaves of Guiera senegalensis J.F. gmel (combretaceae)

TL;DR: The potent synergistic antimalarial interaction between Guiera senegalensis and two plants commonly associated in traditional remedies: Mitragyna inermis and Pavetta crassipes was evaluated and a synergistic effect was shown between total alkaloids extracted from leaves of Guieranone A and those of Mitragynas inerm is.
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Synthesis and antiprotozoal activity of 4-arylcoumarins.

TL;DR: A large series of 4-arylcoumarins synthesized by Suzuki-Miyaura cross-coupling reaction and evaluated for antiprotozoal activity against Plasmodium falciparum and Leishmania donovani found to strongly inhibit the proliferation of human cell line and/or parasites.