Publications
P312
ChemMedChem 2026, 21, e70338.
Bicyclic Lactams From Chiral Imines: Synthesis, Structural Optimization, and Biological Evaluation of Promising Antileishmanial Agents.
P310
Bioorg. Chem. 2026, 176, 109839.
Insights into a new class of antileishmanial compounds: an in vitro and in silico study of 1,2,4-oxadiazol-5(4H)-one derivatives.
P309
Bioorg. Med. Chem. 2026, 139, 118678.
5,6,7,8-Tetrahydroimidazo[1,2-a]pyrazine-based thiosemicarbazones as anti-Trypanosoma cruzi agents.
P300
RSC Med. Chem. 2025, 16, 3746–3763.
Pharmacophore-guided optimization of the hit compound CTN1122 in the design of promising imidazo[1,2-a]pyrazine derivatives targeting the casein kinase 1 for antileishmanial therapy
P290
ChemMedChem. 2025, 20, e202400862.
Investigating the C2 modulation of the imidazo[1,2-a]pyrazine-based hit compound CTN1122: synthesis, in vitro antileishmanial activity, cytotoxicity and casein kinase 1 inhibition.
P289
Pharmaceuticals. 2025, 18, 125.
2-Aminothiophene derivatives -New drug canditates against leismaniasis: Drug design, synthesis, pharmacomodulation, and antileishmanial activity.
P287
Eur. J. Med. Chem. Rep. 2024, 12, 100228.
Biological properties and in silico studies of thiazolopyrimidine derivatives active against visceral and cutaneous Leishmania spp. amastigote forms.
P279
Pharmaceuticals 2024, 17, 516.
FRET Assays for the Identification of C. albicans HSP90-Sba1 and Human HSP90α-p23 Binding Inhibitors.
P275
Microorganisms 2023, 11, 2837.
Is the C-terminal domain an effective and selective target for the design of Hsp90 inhibitors against Candida yeast?
P269
Nat. Prod. Res. 2023
Phytochemical, antileishmanial, antifungal and cytotoxic profiles of Thymelaea tartonraira (L.) All. extracts.
P268
Future Microbiol. 2023, 18, 1225-1233.
Antifungal efficacy of imidazo[1,2-a]pyrazine based thiosemicarbazones and thiazolidinediones against Sporothrix species.
P267
Chem. Biodivers. 2023, 20, e202200944;
New specific α-glucosidase inhibitor flavonoid from Thymelaea tartonraira leaves: structure elucidation, biological and molecular docking studies.
P250
Phytochem. Lett. 2022, 50, 57-60.
Amino ether analogues of 4,4′-dihydroxy-3-methoxy-6,7′-cyclolignan and their activity against drug-resistant bacteria.
P244
Letter to the Editor, Quim. Nova 2022, 45, 1-3.
The Franco-Brazilian Network on Natural Products (FB2NP): a new network promoting cooperation and exchanges in natural products research.
P240
Molecules 2021, 26, 6572.
Dibenzofuran derivatives inspired from cercosporamide as dual inhibitors of Pim and CLK1 kinases.
doi: 10.3390/molecules26216572
P239
Chem. Biol. Interact. 2021, 347, 109597.
Synthesis, anticancer activity and mechanism of action of new phthalimido-1,3-thiazole derivatives.
doi: 10.1016/j.cbi.2021.109597
P237
Phytochem. Lett. 2021, 43, 212-218.
New cyclolignans of Larrea tridentata and their antibacterial and cytotoxic activities.
doi: 10.1016/j.phytol.2021.04.013
P234
Med. Chem. Res. 2021, 30, 152-162.
Antimicrobial and anti-leishmanial activities of extracts and some constituents from the leaves of Solanum chrysotrichum Schldl.
doi: 10.1007/s00044-020-02648-8
P232
Chem. Biol. Interact. 2021, 333, 109316.
Streptomyces hygroscopicus UFPEDA 3370: a valuable source of the potent cytotoxic agent nigericin and its evaluation against human colorectal cancer cells.
doi: 10.1016/j.cbi.2020.109316
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
Autres publications scientifiques
PS38
J. Med. Chem. 2025, 68, 2045–2047.
Shaping future medicinal chemists: Perspectives from European schools of Pharmacy within the GP2A network.
PS37
Pharmaceuticals 2025, 18, 837.
New insights into the anticancer effects and toxicogenomic safety of two β-Lapachone derivatives.
PS09
Antiinflamm. Antiallergy Agents Med. Chem. 2022, 21, 135-151.
Effects of acylhydrazone derivatives on experimental pulmonary inflammation by chemical sensitization.
PS04
Curr. Top. Med. Chem. 2022, 22, 247-258.
Antinociceptive effects of aza-bicyclic isoxazoline-acylhydrazone derivatives in different models of nociception in mice.
Brevets
B12.
Nouveaux dérivés indoliques, leur procédé de préparation et les compositions pharmaceutiques qui les contiennent.
Brevet Français, déposé le 18 octobre 2006, sous le n° 06/09114.
B11.
Nouveaux dérivés indoliques, leur procédé de préparation et les compositions pharmaceutiques qui les contiennent.
Brevet Français, déposé le 18 octobre 2006, sous le n° 06/09113.
B15.
Novel Naphthyridine derivatives and the use thereof as kinase inhibitors.
PCT Int. Appl. WO 2011064250, 2011.
Thèse
T01.
Synthèse et évaluation pharmacologique de dérivés indoliques à activités immunosuppressive et antitumorale.
Nantes, 23 novembre 1999.