45 results on '"Logé, Cédric"'
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2. New azole antifungals with a fused triazinone scaffold
3. Potassium 6-Oxo-7,13,16,22-tetraazatetracyclo[12.6.2.18,12.017,21]tricosa-1(20),8(23),9,11,14,16,18,21-octaen-2-yne-15-carboxylate
4. Structure-based design of novel quinoxaline-2-carboxylic acids and analogues as Pim-1 inhibitors
5. Potassium 6-Oxo-7,13,16,22-tetraazatetracyclo[12.6.2.1 8,12.0 17,21 ]tricosa-1(20),8(23),9,11,14,16,18,21-octaen-2-yne-15-carboxylate.
6. Development of new highly potent imidazo[1,2-b]pyridazines targeting Toxoplasma gondii calcium-dependent protein kinase 1
7. 4-cholesten-3-one decreases breast cancer cell viability and alters membrane raft-localized EGFR expression by reducing lipogenesis and enhancing LXR-dependent cholesterol transporters
8. Synthesis and molecular modelling studies of 8-arylpyrido[3′,2′:4,5]thieno[3,2-d]pyrimidin-4-amines as multitarget Ser/Thr kinases inhibitors
9. Novel synthesis of angular thiazolo[5,4-f] and [4,5-h]quinazolines, preparation of their linear thiazolo[4,5-g] and [5,4-g]quinazoline analogs
10. Synthesis and biological evaluation of new 5-benzylated 4-oxo-3,4-dihydro-5H-pyridazino[4,5-b]indoles as PI3Kα inhibitors
11. Anti-proliferative and Pro-apoptotic Effect of Dichloromethane Extract of Octopus vulgaris By-Products on Human Breast Cancer Cell Lines
12. Dibenzofuran Derivatives Inspired from Cercosporamide as Dual Inhibitors of Pim and CLK1 Kinases
13. Exosomes as New Biomarkers and Drug Delivery Tools for the Prevention and Treatment of Various Diseases: Current Perspectives
14. Homology modeling of MT 1 and MT 2 receptors
15. Novel 9-oxo-thiazolo[5,4- f]quinazoline-2-carbonitrile derivatives as dual cyclin-dependent kinase 1 (CDK1)/glycogen synthase kinase-3 (GSK-3) inhibitors: Synthesis, biological evaluation and molecular modeling studies
16. Synthesis of 3,5-bis(2-indolyl)pyridine and 3-[(2-indolyl)-5-phenyl]pyridine derivatives as CDK inhibitors and cytotoxic agents
17. New Quinoxaline Derivatives as Dual Pim-1/2 Kinase Inhibitors: Design, Synthesis and Biological Evaluation
18. Synthesis of 5,5′-Dithiobis(2-nitrobenzamides)as Alternative Substrates for Trypanothione Reductase and Thioredoxin Reductase: A Microtiter Colorimetric Assay for Inhibitor Screening
19. Synthesis of new pyridazino[4,5-b]indol-4-ones and pyridazin-3(2H)-one analogs as DYRK1A inhibitors
20. Discovery of (7-aryl-1,5-naphthyridin-2-yl)ureas as dual inhibitors of ERK2 and Aurora B kinases with antiproliferative activity against cancer cells
21. The amino acid substitution N136Y inCandida albicanssterol 14alpha-demethylase is involved in fluconazole resistance
22. Activation of EGFR by small compounds through coupling the generation of hydrogen peroxide to stable dimerization of Cu/Zn SOD1
23. The amino acid substitution N136Y in Candida albicans sterol 14alpha-demethylase is involved in fluconazole resistance.
24. Screening and discovery of nitro-benzoxadiazole compounds activating epidermal growth factor receptor (EGFR) in cancer cells
25. Design of new antifungal agents: synthesis and evaluation of 1-[(1 H-indol-5-ylmethyl)amino]-2-phenyl-3-(1 H-1,2,4-triazol-1-yl)propan-2-ols
26. Synthesis and structure–activity relationships of 2-phenyl-1-[(pyridinyl- and piperidinylmethyl)amino]-3-(1 H-1,2,4-triazol-1-yl)propan-2-ols as antifungal agents
27. Discovery of a Novel Broad-Spectrum Antifungal Agent Derived from Albaconazole
28. Design, synthesis, and evaluation of 1-( N-benzylamino)-2-phenyl-3-(1 H-1,2,4-triazol-1-yl)propan-2-ols as antifungal agents
29. Study of N1-alkylation of indoles from the reaction of 2(or 3)-aminoindole-3-(or 2)carbonitriles with DMF-dialkylacetals
30. Design, Synthesis, and Biological Evaluation of 1‐[(Biarylmethyl)methylamino]‐2‐(2,4‐difluorophenyl)‐3‐(1H‐1,2,4‐triazol‐1‐yl)propan‐2‐ols as Potent Antifungal Agents: New Insights into Structure–Activity Relationships
31. Design, Synthesis, and in vitro Antifungal Activity of 1-[(4-Substituted-benzyl)methylamino]-2-(2,4-difluorophenyl)-3-(1H-1,2,4-triazol-1-yl)propan-2-ols
32. Synthesis and in vitro antifungal evaluation of 2-(2,4-difluorophenyl)-1-[(1H-indol-3-ylmethyl)methylamino]-3-(1H-1,2,4-triazol-1-yl)propan-2-ols
33. A convenient synthesis of 5-arylamino-4H-pyran-4-ones using palladium-catalyzed amination
34. Design of new antifungal agents: synthesis and evaluation of 1-[(1H-indol-5-ylmethyl)amino]-2-phenyl-3-(1H-1,2,4-triazol-1-yl)propan-2-ols
35. Synthesis and structure–activity relationships of 2-phenyl-1-[(pyridinyl- and piperidinylmethyl)amino]-3-(1H-1,2,4-triazol-1-yl)propan-2-ols as antifungal agents
36. Homology modeling of MT1 and MT2 receptors
37. Design, synthesis, and evaluation of 1-(N-benzylamino)-2-phenyl-3-(1H-1,2,4-triazol-1-yl)propan-2-ols as antifungal agents
38. Thiazolo[5,4-f]quinazolin-9-ones, inhibitors of glycogen synthase kinase-3
39. Potent and Selective Farnesyl Transferase Inhibitors
40. Synthesis and Pharmacological Study of Rho-Kinase Inhibitors: Pharmacomodulations on the Lead Compound Fasudil
41. Rho-kinase Inhibitors: Pharmacomodulations on the Lead Compound Y-32885
42. Design, Synthesis, and Biological Evaluation of 1-[(Biarylmethyl)methylamino]-2-(2,4-difluorophenyl)-3-(1 H-1,2,4-triazol-1-yl)propan-2-ols as Potent Antifungal Agents: New Insights into Structure-Activity Relationships.
43. Design, Synthesis, and in vitro Antifungal Activity of 1-[(4-Substituted-benzyl)methylamino]-2-(2,4-difluorophenyl)-3-(1 H-1,2,4-triazol-1-yl)propan-2-ols.
44. Synthesis and in vitro antifungal evaluation of 2-(2,4-difluorophenyl)-1-[(1 H-indol-3-ylmethyl)methylamino]-3-(1 H-1,2,4-triazol-1-yl)propan-2-ols.
45. Homology modeling of MT1 and MT2 receptors
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