All Stories

  1. New Serotoninergic Ligands Containing Indolic and Methyl Indolic Nuclei: Synthesis and In Vitro Pharmacological Evaluation
  2. Design of Sphingosine Kinases Inhibitors: Challenges and Recent Developments
  3. The Role of 5-HT1A Receptor in Cancer as a New Opportunity in Medicinal Chemistry
  4. Synthesis of Arylpiperazine Derivatives as Protease Activated Receptor 1 Antagonists and Their Evaluation as Antiproliferative Agents
  5. Fragment-based de novo design of a cystathionine γ-lyase selective inhibitor blocking hydrogen sulfide production
  6. Quantification of 3α-hydroxytibolone in human plasma by high performance liquid chromatography coupled to electrospray ionization tandem mass spectrometry (HPLC-ESI-MS/MS): Application in a bioequivalence study in healthy postmenopausal volunteers
  7. 5-HT2 receptor affinity, docking studies and pharmacological evaluation of a series of 1,3-disubstituted thiourea derivatives
  8. Level, potential sources of polycyclic aromatic hydrocarbons (PAHs) in particulate matter (PM10) in Naples
  9. Synthesis, in vitro and in vivo pharmacological evaluation of serotoninergic ligands containing an isonicotinic nucleus
  10. Identification of a novel selective CSE inhibitor through a combined pharmacological and metabolomic approach
  11. Synthesis, biological evaluation, and docking studies of PAR2-AP-derived pseudopeptides as inhibitors of kallikrein 5 and 6
  12. Synthesis andIn VitroPharmacological Evaluation of Novel 2-Hydroxypropyl-4-arylpiperazine Derivatives as Serotoninergic Ligands
  13. 5-HT 1A Receptor: An Old Target as a New Attractive Tool in Drug Discovery from Central Nervous System to Cancer
  14. Identification of a pepducin acting as S1P3 receptor antagonist
  15. Kallikrein Protease Activated Receptor (PAR) Axis: An Attractive Target for Drug Development
  16. Synthesis of benzamide derivatives and their evaluation as antiprion agents
  17. New potent 5-HT2A receptor ligands containing an N′-cyanopicolinamidine nucleus: Synthesis and in vitro pharmacological evaluation
  18. ChemInform Abstract: Synthesis by Microwave Irradiation and Binding Properties of Novel 5-HT1A Receptor Ligands.
  19. Thrombin receptors and their antagonists: an update on the patent literature
  20. New 5-HT1A receptor ligands containing a N′-cyanoisonicotinamidine nucleus: Synthesis and in vitro pharmacological evaluation
  21. Efficient microwave combinatorial synthesis of novel indolic arylpiperazine derivatives as serotoninergic ligands
  22. A nitro-arginine derivative of trimebutine (NO2-Arg-Trim) attenuates pain induced by colorectal distension in conscious rats
  23. Efficient microwave-assisted synthesis of 4-amino-2-benzazepin-3-ones as conformationally restricted dipeptide mimetics
  24. Synthesis and pharmacological evaluation of peptide-mimetic protease-activated receptor-1 antagonists containing novel heterocyclic scaffolds
  25. ChemInform Abstract: Design and Synthesis of Potential β-Sheet Nucleators via Suzuki Coupling Reaction.
  26. Synthesis and Pharmacological Evaluations of Sildenafil Analogues for Treatment of Erectile Dysfunction
  27. Synthesis andIn-vitroPharmacological Evaluation of New 5-HT1AReceptor Ligands Containing a Benzotriazinone Nucleus
  28. Design and synthesis of potential β-sheet nucleators via Suzuki coupling reaction
  29. Microwave Solvent-Free Regioselective 1,3-Dipolar Cycloaddition in the Synthesis of 1,4-Substituted[1,2,3]-triazoles as Amide Bond Isosteres.
  30. Pharmacokinetic Profile of Atenolol Aspirinate
  31. Microwave solvent free regioselective 1,3 dipolar cycloaddition in the synthesis of 1,4 substituted [1,2,3]-triazoles as amide bond isosteres
  32. Effect of positive charge in VIP16γ-glutamyl diamino derivatives on hVPAC1 and hVPAC2 receptor function
  33. Conformation–activity relationship of peptide T and new pseudocyclic hexapeptide analogs
  34. Synthesis of 2-Methyl-3-indolylacetic Derivatives as Anti-Inflammatory Agents That Inhibit Preferentially Cyclooxygenase 1 without Gastric Damage
  35. Synthesis by Microwave Irradiation and Antidiarrhoeal Activity of Benzotriazinone and Saccharine Derivatives.
  36. Synthesis, Pharmacological Evaluation, and Molecular Modeling Studies of Novel Peptidic CAAX Analogues as Farnesyl-Protein-Transferase Inhibitors
  37. Effects ofN- andC-terminal addition of oligolysines or native loop residues on the biophysical properties of transmembrane domain peptides from a G-protein coupled receptor
  38. Synthesis by Microwave Irradiation and Antidiarrhoeal Activity of Benzotriazinone and Saccharine Derivatives
  39. New 5-Hydroxytryptamine 1A Receptor Ligands Containing a Norbornene Nucleus:  Synthesis and in Vitro Pharmacological Evaluation
  40. Efficient Microwave Combinatorial Parallel and Nonparallel Synthesis of N-Alkylated Glycine Methyl Esters as Peptide Building Blocks
  41. Synthetic peptides as probes for conformational preferences of domains of membrane receptors
  42. A Valuable Synthesis of Reduced Peptide Bond by Microwave Irradiation
  43. Synthesis by microwave irradiation of a substituted benzoxazine parallel library with preferential relaxant activity for guinea pig trachealis
  44. Evidence for a protective role played by the Na+/Ca2+ exchanger in cerebral ischemia induced by middle cerebral artery occlusion in male rats
  45. Synthesis of N α -Fmoc N , N ′-bis-Boc-5-, 6- and 8-guanyl-1,2,3,4-tetrahydroisoquinoline-3-carboxylic Acid (5-GTIC, 6-GTIC and 8-GTIC)
  46. PAR1 antagonism protects against experimental liver fibrosis. Role of proteinase receptors in stellate cell activation
  47. A convenient strategy of dimerization by microwave heating and using 2,5-diketopiperazine as scaffold
  48. A convenient synthesis by microwave irradiation of an active metabolite (EXP-3174) of losartan
  49. A convenient synthesis by microwave heating and pharmacological evaluation of novel benzoyltriazole and saccharine derivatives as 5-HT1A receptor ligands
  50. Design of Inhibitors for Human Tissue Kallikrein Using Non-Natural Aromatic and Basic Amino Acids
  51. Minimal structural requirements for agonist activity of PAR-2 activating peptides
  52. Synthesis of novel anti-inflammatory peptides derived from the amino-acid sequence of the bioactive protein SV-IV
  53. A convenient synthesis of N-Fmoc-N,N′-bis-Boc-7-guanyl-1,2,3,4-tetrahydro-isoquinoline-3-carboxylic acid (Fmoc-N,N′-bis-Boc-7-guanyl-Tic-OH, GTIC)
  54. Probing the shape of a hydrophobic pocket in the active site of?-opioid antagonists
  55. Synthesis and structure–activity of antisense peptides corresponding to the region for CaM-binding domain of the inducible nitric oxide synthase1Symbols and abbreviations are in accord with recommendations from [1]
  56. Synthesis of new 1,2,3-benzotriazin-4-one-arylpiperazine derivatives as 5-HT1A serotonin receptor ligands
  57. Synthesis and biological activity of pseudopeptides inhibitors of Ras farnesyl transferase containing unconventional amino acids
  58. Influence of Natural Loop Residues or Oligolysines on the Biophysical Properties of Transmembrane Domains of a G Protein-Coupled Receptor