Maria Candida Monteiro De Aguiar

Dr. Maria Candida Monteiro De Aguiar


Research Focus & Metrics

Academic Career Length

15Years (2012-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 April 2012 in SLAS Discovery
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Journal Article
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MAMaria Candida Monteiro De Aguiar
Maria Candida Monteiro De Aguiar
MCMercedes De La Cruz
Mercedes De La Cruz
JCJuan Cantizani
Juan Cantizani
CMCatalina Moreno
Catalina Moreno
Ruben TormoRuben Tormo
Ruben Tormo
FVFrancisca Vicente
Francisca Vicente
Natural products are an inexhaustible source for drug discovery. However, the validation and selection of primary screening assays are vital to guarantee a selection of extracts or molecules with relevant pharmacological action and worthy of following up. The assay must be rapid, simple, easy to implement, and produce quick results and preferably at a low cost. In this work, we developed and validated a colorimetric microtiter assay using the resazurin viability dye. The parameters of the resazurin method for high-throughput screening (HTS) using natural extracts against Aspergillus fumigatus were optimized and set up. The extracts plus RPMI-1640 modified medium containing the spores and 0.002% resazurin were added per well. The fluorescence was read after 24 to 30 h of incubation. The resazurin proved to be as suitable as Alamar Blue for determining the minimal inhibitory concentration of different antifungals against A. fumigatus and effective to analyze fungicidal and fungistatic compounds. An HTS of 12 000 microbial extracts was carried out against two A. fumigatus strains, and 2.7% of the extracts displayed antifungal activity. Our group has been the first to use this methodology for screening a collection of natural extracts to identify compounds with antifungal activity against the medically important human pathogen A. fumigatus.

6 May 2013 in Marine Drugs
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Journal Article
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CACoralie Audoin
Coralie Audoin
DBDominique Bonhomme
Dominique Bonhomme
Julijana IvanisevicJulijana Ivanisevic
Julijana Ivanisevic
MCMercedes De La Cruz
Mercedes De La Cruz
BCBastien Cautain
Bastien Cautain
Olivier ThomasOlivier Thomas
Olivier Thomas
The chemical investigation of the recently described Mediterranean Homoscleromorpha sponge Oscarella balibaloi revealed an original family of five closely related glucosylated sesterterpenes 1–4, named balibalosides. Their structure elucidation was mainly inferred from NMR and HRMS data analyses. Balibalosides differ by the pattern of acetyl substitutions on the three sugar residues linked to the same aglycone sesterterpenoid core. From a biosynthetic perspective, these compounds may represent intermediates in the pathways leading to more complex sesterterpenes frequently found in Dictyoceratida, a sponge Order belonging to Demospongiae, a clade which is phylogenetically distinct from the Homoscleromorpha. While steroid and triterpenoid saponins were already well known from marine sponges, balibalosides are the first examples of glycosilated sesterterpenes.