All Stories

  1. In Situ Formation of Cationic π-Allylpalladium Precatalysts in Alcoholic Solvents: Application to C–N Bond Formation
  2. Design, Synthesis and Biological Evaluation of Arylpyridin-2-yl Guanidine Derivatives and Cyclic Mimetics as Novel MSK1 Inhibitors. An Application in an Asthma Model
  3. Comprehensive overview of biased pharmacology at the opioid receptors: biased ligands and bias factors
  4. Diastereoselective Synthesis of Nonplanar 3-Amino-1,2,4-oxadiazine Scaffold: Structure Revision of Alchornedine
  5. Mitochondria modulatory effects of new TSPO ligands in a cellular model of tauopathies
  6. Fukuyama Cross-Coupling Approach to Isoprekinamycin: Discovery of the Highly Active and Bench-Stable Palladium Precatalyst POxAP
  7. Induction of ATP Release, PPIX Transport, and Cholesterol Uptake by Human Red Blood Cells Using a New Family of TSPO Ligands
  8. Aminoguanidine Hydrazone Derivatives as Nonpeptide NPFF1 Receptor Antagonists Reverse Opioid Induced Hyperalgesia
  9. Heteroarylguanidines as Allosteric Modulators of ASIC1a and ASIC3 Channels
  10. χ-Space Screening of Dermorphin-Based Tetrapeptides through Use of Constrained Arylazepinone and Quinolinone Scaffolds
  11. Development of DipeptidichGPR54 Agonists
  12. RF-amide neuropeptides and their receptors in Mammals: Pharmacological properties, drug development and main physiological functions
  13. Opioid adjuvant strategy: improving opioid effectiveness
  14. CMTX Disorder and CamKinase
  15. Synthesis of 3-amino-3,4-dihydro-1H-quinolin-2-ones through regioselective palladium-catalyzed intramolecular cyclization
  16. Erratum to: CMTX1 patients’ cells present genomic instability corrected by CamKII inhibitors
  17. Effects of systematic N-terminus deletions and benzoylations of endogenous RF-amide peptides on NPFF1R, NPFF2R, GPR10, GPR54 and GPR103
  18. Design and validation of a homogeneous time-resolved fluorescence cell-based assay targeting the ligand-gated ion channel 5-HT3A
  19. The long-lasting love affair between the budding yeastSaccharomyces cerevisiaeand the Epstein-Barr virus
  20. Neuropeptide FF receptors as novel targets for limbic seizure attenuation
  21. CMTX1 patients’ cells present genomic instability corrected by CamKII inhibitors
  22. ChemInform Abstract: Access to 4-Alkylaminopyridazine Derivatives via Nitrogen-Assisted Regioselective Pd-Catalyzed Reactions.
  23. Development of a Peptidomimetic Antagonist of Neuropeptide FF Receptors for the Prevention of Opioid-Induced Hyperalgesia
  24. Neuropeptide FF and prolactin-releasing peptide decrease cortical excitability through activation of NPFF receptors
  25. ChemInform Abstract: t-BuXPhos: A Highly Efficient Ligand for Buchwald-Hartwig Coupling in Water.
  26. Rapid and scalable synthesis of innovative unnatural α,β or γ-amino acids functionalized with tertiary amines on their side-chains
  27. A Yeast/DrosophilaScreen to Identify New Compounds Overcoming Frataxin Deficiency
  28. Access to 4-Alkylaminopyridazine Derivatives via Nitrogen-Assisted Regioselective Pd-Catalyzed Reactions
  29. Structure–Activity Relationship Study around Guanabenz Identifies Two Derivatives Retaining Antiprion Activity but Having Lost α2-Adrenergic Receptor Agonistic Activity
  30. ChemInform Abstract: Buchwald-Hartwig Reactions in Water Using Surfactants.
  31. ChemInform Abstract: Fully Regiocontrolled Polyarylation of Pyridine.
  32. CamKII inhibitors reduce mitotic instability, connexon anomalies and progression of the in vivo behavioral phenotype in transgenic animals expressing a mutated Gjb1 gene
  33. Buchwald–Hartwig reactions in water using surfactants
  34. ChemInform Abstract: Nucleophilic Substitution of Azide Acting as a Pseudo Leaving Group: One-Step Synthesis of Various Aza Heterocycles.
  35. Fully Regiocontrolled Polyarylation of Pyridine
  36. t-BuXPhos: a highly efficient ligand for Buchwald–Hartwig coupling in water
  37. Neuropeptide FF receptors are implicated in epileptic seizures
  38. ChemInform Abstract: N-Heteroarylation of Chiral α-Aminoesters by Means of Palladium-Catalyzed Buchwald-Hartwig Reaction.
  39. Endogenous mammalian RF-amide peptides, including PrRP, kisspeptin and 26RFa, modulate nociception and morphine analgesia via NPFF receptors
  40. Nucleophilic Substitution of Azide Acting as a Pseudo Leaving Group: One-Step Synthesis of Various Aza Heterocycles
  41. N -Heteroarylation of Chiral α-Aminoesters by Means of Palladium-Catalyzed Buchwald–Hartwig Reaction
  42. The neuroprotector kynurenic acid increases neuronal cell survival through neprilysin induction
  43. Synthesis and Antiproliferative Effects of 5,6-Disubstituted Pyridazin-3(2H)-ones Designed as Conformationally Constrained Combretastatin A-4 Analogues
  44. ChemInform Abstract: Palladium-Catalyzed Synthesis of Substituted Pyrido[2,3-d]pyridazines at Positions 5 and 8.
  45. Trisubstitution of pyridine through sequential and regioselective palladium cross-coupling reactions affording analogs of known GPR54 antagonists
  46. Development of sub-nanomolar dipeptidic ligands of neuropeptide FF receptors
  47. Palladium-Catalyzed Synthesis of Substituted Pyrido[2,3-d]pyridazines at Positions 5 and 8
  48. 1-Phenyl-3H-2,3-benzodiazepin-4(5H)-one
  49. ChemInform Abstract: Direct Guanidinylation of Aryl and Heteroaryl Halides via Copper-Catalyzed Cross-Coupling Reaction.
  50. Direct Guanidinylation of Aryl and Heteroaryl Halides via Copper-Catalyzed Cross-Coupling Reaction
  51. Involvement of neuropeptide FF receptors in neuroadaptive responses to acute and chronic opiate treatments
  52. New PDE4 inhibitors based on pharmacophoric similarity between papaverine and tofisopam
  53. ChemInform Abstract: New 3′-Azido-3′-deoxythymidin-5′-yl O-(ω-Hydroxyalkyl) Carbonate Prodrugs: Synthesis and Anti-HIV Evaluation.
  54. ChemInform Abstract: Design of Potential New HIV Protease Inhibitors: Enantioconvergent Synthesis of New Pyrrolidin-3-ol, and Pyrrolidin-3-one Peptide Conjugates.
  55. Pharmacological characterization of the mouse NPFF2 receptor
  56. ChemInform Abstract: Synthesis and Reactivity of 2,3-Dihydro-1H-2,3-benzodiazepine-1,4(5H)-dione.
  57. ChemInform Abstract: 6-endo-Dig Cyclization of Heteroarylesters to Alkynes Promoted by Lewis Acid Catalyst in the Presence of Broensted Acid.
  58. 6-endo-dig Cyclization of heteroarylesters to alkynes promoted by Lewis acid catalyst in the presence of Brønsted acid
  59. Synthesis and Reactivity of 2,3-Dihydro-1H-2,3-benzodiazepine-1,4(5H)-dione
  60. Microwave-Assisted Cyclic Amidine Synthesis Using TiCl4.
  61. Microwave-assisted cyclic amidine synthesis using TiCl4
  62. New 2-Bromomethyl-8-substituted-benzo[c]chromen-6-ones. Synthesis and Biological Properties.
  63. The initial substrate-binding site of γ-secretase is located on presenilin near the active site
  64. Substituted thiazolamide coupled to a redox delivery system: a new γ-secretase inhibitor with enhanced pharmacokinetic profile
  65. New 2-bromomethyl-8-substituted-benzo[c]chromen-6-ones. Synthesis and biological properties
  66. N-Acyl Substituted 7-Amino-4-chloroisocoumarin: A Peptide Degradation Model via an Imide Mechanism.
  67. Discovery of a Subnanomolar Helicald-Tridecapeptide Inhibitor of γ-Secretase
  68. P4-347 Discovery of a subnanomolar inhibitor of γ-secretase
  69. N-Acyl substituted 7-amino-4-chloroisocoumarin: A peptide degradation model via an imide mechanism
  70. Synthesis of new 3-alkoxy-7-amino-4-chloro-isocoumarin derivatives as new β-amyloid peptide production inhibitors and their activities on various classes of protease
  71. Reactivity studies of 3-alkoxy-7-amino-4-chloroisocoumarins (β-amyloid peptide inhibitors)versus different classes of amines
  72. Novel synthesis of 3,4-dihydro-5-bromo[1,4]oxazin-2-one derivatives, new protease inhibitor scaffold
  73. New β-strand macrocyclic peptidomimetic analogues containing α-(O-, S- or NH-)aryl substituted glycine residues: synthesis, chemical and enzymatic properties
  74. Synthesis and Antiviral Activity of New Anti-HIV Amprenavir Bioisosteres
  75. New Non-Peptidic Inhibitors of γ-Secretase Abolish Aβ Production Without Modifying Notch Cleavage
  76. New 3‘-Azido-3‘-deoxythymidin-5‘-yl O -( ω -Hydroxyalkyl) Carbonate Prodrugs:  Synthesis and Anti-HIV Evaluation
  77. Design of potential new HIV protease inhibitors: enantioconvergent synthesis of new pyrrolidin-3-ol, and pyrrolidin-3-one peptide conjugates