Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Chantal Beney"'
Autor:
Anne-Marie Mariotte, Pascale Cégiéla, Christine Bayet, Gilbert Cartier, Chantal Beney, Serge Michalet, Marie-Geneviève Dijoux-Franca, Etienne Tsamo, Diderot Noungoué‐Tchamo, Laëtitia Payen‐Fattaccioli
Publikováno v:
Helvetica Chimica Acta
Helvetica Chimica Acta, 2008, 91 (6), pp.1106-1117. ⟨10.1002/hlca.200890118⟩
Helvetica Chimica Acta, Wiley, 2008, 91 (6), pp.1106-1117. ⟨10.1002/hlca.200890118⟩
Helv. Chim. Acta.
Helv. Chim. Acta., 2008, 91, pp.1106-1117
Helvetica Chimica Acta, 2008, 91 (6), pp.1106-1117. ⟨10.1002/hlca.200890118⟩
Helvetica Chimica Acta, Wiley, 2008, 91 (6), pp.1106-1117. ⟨10.1002/hlca.200890118⟩
Helv. Chim. Acta.
Helv. Chim. Acta., 2008, 91, pp.1106-1117
Phytochemical investigation of barks of Christiana africana led to the identification of cyclopeptide alkaloids, flavonoids, coumarinolignans, iridoids, sesquiterpenoids, and triterpenes. This plant was classified so far in the Tiliaceae family. This
Autor:
Bruno Bonaz, Chantal Beney, Ahcène Boumendjel, Romain Haudecoeur, Antoine Depaulis, Florence Souard, Marc Le Borgne, Tanguy Chabrol, Michel De Waard, Richard J. Robins, Elisabeth Ngo Bum, Soura Challal, Thierry Lomberget, Catherine Lavaud, Laurence Marcourt, Germain Sotoing Taiwe, Jean-Luc Wolfender, Emerson Ferreira Queiroz, Valérie Sinniger
Publikováno v:
Angewandte Chemie International Edition
Angewandte Chemie International Edition, 2013, 52 (45), pp.11780-4. ⟨10.1002/anie.201305697⟩
Angewandte Chemie International Edition, Wiley-VCH Verlag, 2013, 52 (45), pp.11780-4. ⟨10.1002/anie.201305697⟩
Angewandte Chemie International Edition, 2013, 52 (45), pp.11780-4. ⟨10.1002/anie.201305697⟩
Angewandte Chemie International Edition, Wiley-VCH Verlag, 2013, 52 (45), pp.11780-4. ⟨10.1002/anie.201305697⟩
moderate to severe pain without any known side effects. [8, 9] It was designed by a simplification of the structure of morphine that kept the pharmacophoric elements responsible for the analgesic effect. Herein, we describe the isolation of tramadol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5ccf79fdce1462514ca648adc97c263b
https://www.hal.inserm.fr/inserm-00874145
https://www.hal.inserm.fr/inserm-00874145
Autor:
Nabajyoti Deka, Chantal Beney, Attilio Di Pietro, Doriane Trompier, Hélène Baubichon-Cortay, Anne-Marie Mariotte, Ahcène Boumendjel, Martin A. Lawson
Publikováno v:
Chemical and Pharmaceutical Bulletin. 50:854-856
A series of 4-hydroxy-6-methoxyaurones and 4,6-dimethoxyaurones has been synthesised and tested for their binding affinity toward the nucleotide-binding domain of P-glycoprotein, an ABC (ATP-Binding Cassette) transporter which mediates the resistance
Autor:
Frederic Bois, Chantal Beney, Ahcène Boumendjel, G. Conseil, Attilio Di Pietro, Anne-Marie Mariotte
Publikováno v:
Bioorganic and Medicinal Chemistry Letters
Bioorganic and Medicinal Chemistry Letters, Elsevier, 2001, 11, pp.75-77
Bioorganic and Medicinal Chemistry Letters, Elsevier, 2001, 11, pp.75-77
Starting from the interaction of galangin (3,5,7-trihydroxyflavone) with a cytosolic nucleotide-binding domain of P-glycoprotein, a series of flavonol derivatives was synthesized and tested for their binding affinity towards the same target. The 5,7-
Publikováno v:
ChemInform. 29
phenyl(N-methoxy-N-methylcarbamoylmethyl)sulfoxide 1 is prepared in 2 steps starting from N-methoxy-N-methylchloroacetamide and thiophenol. Reagent 1 is useful for homologation of alkyl halides to α,β-unsaturated N-methoxy-N-methylamide compounds.
Publikováno v:
ChemInform. 30
Publikováno v:
ChemInform. 32
Publikováno v:
ChemInform. 33
Autor:
Chantal Beney, Ahcene Boumendjel, Sabrina Okombi, Séverine Chevalley, Florence Souard, Alexis Valentin
Publikováno v:
Bioorganicmedicinal chemistry. 18(15)
We report the synthesis and in vitro antiplasmodial activity of 35 compounds, designed as analogues of the naturally occurring aurones. Several of these analogues showed submicromolar antimalarial activity against a chloroquine-resistant strain of Pl
Publikováno v:
Tetrahedron Letters. 41:7037-7039
The synthesis of 2-aryl-3,5,7-trimethoxy-4-quinolones was accomplished in three steps starting from 3,5-dimethoxyaniline and an aroyl chloride. These structures might be used as potential flavonol analogs.