Publications
P313
Medical Mycology, 2026, 64, myag094
A new MRR1 gain-of-function mutation involved in cross-resistance to antifungal agents in the fungal priority pathogen Candida parapsilosis.
P309
Bioorg. Med. Chem. 2026, 139, 118678.
5,6,7,8-Tetrahydroimidazo[1,2-a]pyrazine-based thiosemicarbazones as anti-Trypanosoma cruzi agents.
P302
Inorg. Chem., 2025, 64, 16192-16203.
Synthesis and Biological Evaluation of Itraconazole Derivatives: Design in an Old Scaffold.
P301
J. Med. Mycol. 2025, 101583.
A One Health Perspective on Diutina catenulata: Phenotypic Traits, Stress Sensitivity, and Virulence Across Diverse Isolates.
P278
Antimicrob. Agents Chemother. 2024, e0002224.
Precise genome editing underlines the distinct contributions of mutations in ERG11, ERG3, MRR1, and TAC1 genes to antifungal resistance in Candida parapsilosis.
P273
In: Barreiro, C., Barredo, JL. (eds) Microbial Steroids. Methods in Molecular Biology, vol 2704. Humana, New York, NY. 2023
Fungal Sterol Analyses by Gas Chromatography–Mass Spectrometry Using Different Derivatives.
P268
Future Microbiol. 2023, 18, 1225-1233.
Antifungal efficacy of imidazo[1,2-a]pyrazine based thiosemicarbazones and thiazolidinediones against Sporothrix species.
P246
Microorganisms. 2022, 10, 104.
Impact of TR34/L98H, TR46/Y121F/T289A and TR53 alterations in azole‐resistant Aspergillus fumigatus on sterol composition and modifications after In Vitro exposure to itraconazole and voriconazole.
P240
Molecules 2021, 26, 6572.
Dibenzofuran derivatives inspired from cercosporamide as dual inhibitors of Pim and CLK1 kinases.
doi: 10.3390/molecules26216572
P231
Eur. J. Med. Chem. 2021, 210, 112956.
In vitro identification of imidazo[1,2-a]pyrazine-based antileishmanial agents and evaluation of L. major casein kinase 1 inhibition.
doi: 10.1016/j.ejmech.2020.112956
P220
I 2020, 113366.
Determination of antifungal caspofungin in RPMI-1640 cell culture medium bycolumn-switching HPLC-FLD.
doi : 10.1016/j.jpba.2020.113366
P212
Eur. J. Med. Chem. 2020, 189, 112082.
New Azole Antifungals with a Fused Triazinone Scaffold.
doi: 10.1016/j.ejmech.2020.112082
P208
J. Enzym. Inhib. Med. Chem. 2020, 35, 398-403.
Biological exploration of a novel 1,2,4-triazole-indole hybrid molecule as antifungal agent.
doi: 10.1080/14756366.2019.1705292
P205
Pharmaceuticals 2019, 12, 182;
A decade of antifungal leads from natural products: 2010-2019.
doi:10.3390/ph12040182.
P173
Bioorg. Med. Chem. Lett. 2018, 28, 2250-2255.
Benzofuro[3,2-d]pyrimidines inspired from cercosporamide CaPkc1 inhibitor: synthesis and evaluation of fluconazole susceptibility restoration.
doi: 10.1016/j.bmcl.2018.05.044
Autres publications scientifiques
PS37
Pharmaceuticals 2025, 18, 837.
New insights into the anticancer effects and toxicogenomic safety of two β-Lapachone derivatives.