Zobrazeno 1 - 10
of 32
pro vyhledávání: '"Pierre, Brouant"'
Publikováno v:
Journal of Food Science. 83:2858-2865
Many studies have shown that flavan-3-ols inhibit mammalian alpha-amylases but the published IC50 and Ki values vary up to a thousand times. We therefore tested the effects of 6 pure flavan-3-ols-abundant in green tea-on the activity of pure porcine
Publikováno v:
Journal of food science. 83(11)
Many studies have shown that flavan-3-ols inhibit mammalian alpha-amylases but the published IC
Autor:
Maria‐Jose Rosales, Nadia Bsiri, Latifa Khalifa, Jacques Barbe, Carmen Mascaro, Pierre Brouant, Janina Karolak-Wojciechowska
Publikováno v:
Arzneimittelforschung. 50:163-166
The synthesis of several acridinic thioethers is described. Compounds prepared were tested in vitro as potential drugs against the opportunistic infection known as cryptosporidiosis. With a view to predict activity, the quantitative structure-activit
Autor:
Jacques Barbe, Pierre Brouant, Abdallah Mahamoud, Jacqueline Chevalier, Monique Malléa, Sandrine Alibert-Franco, Jean-Marie Pagès
Publikováno v:
Biochemical Journal. 376:801-805
Over the last decade, MDR (multidrug resistance) has increased worldwide in microbial pathogens by efflux mechanisms, leading to treatment failures in human infections. Several Gram-negative bacteria efflux pumps have been described. These proteinace
Autor:
Delia Dicu, Castelia Cristea, Ioan A. Silberg, Pierre Brouant, Liana Maria Muresan, Ionel Catalin Popescu
Publikováno v:
Electrochimica Acta. 45:3951-3957
Phenothiazine derivatives containing two linearly condensed phenothiazine moieties, 16H,18H-dibenzo[c,l]-7,9-dithia-16,18-diazapentacene (I), dibenzo[c,l]-16,18-diacetyl-7,9-dithia-16,18-diazapentacene (II) dibenzo[c,l]-16,18-dibenzoyl-7,9-dithia-16,
Publikováno v:
Journal of Molecular Structure. 522:263-269
On the basis of structural similarities between various calcium channel antagonists (Verapamil or Diltiazem) a novel series of derivatives belonging to the dibenzodiazocinedione family were designed and synthesised to obtain drugs able to revert mult
Publikováno v:
Acta Crystallographica Section C Crystal Structure Communications. 51:970-974
Maprotiline (ludiomil) is a tetracyclic antidepressant drug which crystallized in DMF as the salt [3-(9,10-dihydro-9,10-ethano-9-anthracenyl)propyl]methylammonium N-[3-(9,10-dihydro-9,10-ethano-9-anthracenyl)propyl]-N-methylcarbamate hemihydrate. The
Autor:
A Crémieux, A.-M. Galy, Derek Sharples, J Chevalier, J. Barbe, J. P. Galy, H Berny, Pierre Brouant
Publikováno v:
Research in Microbiology. 146:73-83
The antimicrobial activity of several new 9-acridinones and 9-thioalkylacridines towards Escherichia coli, Staphylococcus aureus, Mycobacterium smegmatis and Candida albicans was investigated. Minimal inhibitory, bactericidal and fungicidal concentra
Autor:
Maciej Posel, J. P. Galy, J. Barbe, Janina Karolak-Wojciechowska, Abdallah Mahamoud, Pierre Brouant, P. Amiel
Publikováno v:
ChemInform. 27
Publikováno v:
ChemInform. 28
The title compound, 3-(6-chloro-2-methoxy-9-acridinyl)-5-[2-(diethylamino)ethylthio]-1,3,4-thiadiazol-2(3H)-one, C 22 H 23 ClN 4 OS 3 , belongs to a series of new potential antiprotozoal drugs containing the acridine and thiadiazole systems. These tw