Baratte, B.
Publications
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
https://doi.org/10.1039/D5MD00257E
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.
https://doi.org/10.1002/cmdc.202400862
P285
Int. J. Pharm. Res. Al. Sci. 2024, 13, 1-11.
Design and synthesis of functionalized 2,4-diamino-1,3,5-triazines, potential inhibitors involved in immune and inflammatory response.
https://doi.org/10.51847/hsT2C61XWx
P240
Molecules 2021, 26, 6572.
Dibenzofuran derivatives inspired from cercosporamide as dual inhibitors of Pim and CLK1 kinases.
doi: 10.3390/molecules26216572
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
P202
Pharmaceuticals 2019, 12, 169.
Biological evaluation of arylsemicarbazone derivatives as potential anticancer agents.
doi:10.3390/ph12040169
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
P136
Eur. J. Med. Chem. 2015, 103, 381-395.
Synthesis, antileishmanial activity and cytotoxicity of 2,3-diaryl- and 2,3,8-trisubstituted imidazo[1,2-a]pyrazines.
doi: 10.1016/j.ejmech.2015.09.002
Autres publications scientifiques
PS36
Pharmaceuticals 2025, 18, 837.
New insights into the anticancer effects and toxicogenomic safety of two β-Lapachone derivatives.
https://doi.org/10.3390/ph18060837
Brevets
Thèse