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Design, synthesis and biological evaluation of new aryl thiosemicarbazone as antichagasic candidates
(2013-08-27)
The present work reports on the synthesis, biological assaying and docking studies of a series of 12 aryl thiosemicarbazones, which were planned to act over two main enzymes, cruzain and trypanothione reductase. These ...
Design, synthesis and biological evaluation of new aryl thiosemicarbazone as antichagasic candidates
(2013-08-27)
The present work reports on the synthesis, biological assaying and docking studies of a series of 12 aryl thiosemicarbazones, which were planned to act over two main enzymes, cruzain and trypanothione reductase. These ...
Fluorescence analysis of iodinated acetophenone derivatives
(Elsevier B.V., 2015-03-15)
In the present paper the synthesis and optical characterization of iodinated acetophenone, 4-hydroxy-3-iodoacetophenone and 4-hydroxy-3,5-diiodoacetophenone obtained from 4-hydroxyacetophenone, were carried out. the optical ...
Antifungal activity of 4-hydroxy-3-(3-methyl-2- butenyl)acetophenone against Candida albicans: evidence for the antifungal mode of action
(Springer, 2015-10)
The main secondary metabolite of Senecio nutans is 4-hydroxy-3-(3-methyl-2-butenyl)acetophenone (4HMBA). The antifungal activity of this compound and three derivatives was assessed using Candida albicans. 4HMBA exhibited ...
Synthesis of compounds with antiproliferative activity as analogues of prenylated natural products existing in Brazilian propolis
(Elsevier France-editions Scientifiques Medicales ElsevierParisFrança, 2006)
A conformational analysis of some alpha-aryloxy p-substituted-acetophenones: Solvent effects on the nu(co) infrared bands
(Spectroscopy Soc Canada, OttawaOttawaCanadá, 2003)
Bioreduction of Acetophenone Derivatives by Red Marine Algae Bostrychia radicans and B. tenella, and Marine Bacteria Associated
(WILEY-BLACKWELL, 2011)
The biocatalytic reduction of acetophenone derivatives was exploited by using algal biomass from Bostrychia radicans and B. tenella producing exclusively (S)-2-phenylethanols with high enantiomeric excess (> 99% ee). ...
A novel asymmetric reduction of dihydro-beta-carboline derivatives using calix[6]arene/chiral amine as a host complex
(Pergamon-elsevier Science LtdOxfordInglaterra, 2003)