All Stories

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