All Stories

  1. Shedding light on the roles of liver X receptors in cancer by using chemical probes
  2. Laboratory-Scale Preparative Enantioseparations of Pharmaceutically Relevant Compounds on Commercially Available Chiral Stationary Phases for HPLC
  3. The Systems Biology of Transporters - Targeting the Regulatory System for Transporters (FXR/RXR)
  4. N-Decyl-S-trityl-(R)-cysteine, a new chiral selector for “green” ligand-exchange chromatography applications
  5. λ5-Phosphorus-Containing α-Diazo Compounds: A Valuable Tool for Accessing Phosphorus-Functionalized Molecules
  6. The Janus-faced nature of IDO1 in infectious diseases: challenges and therapeutic opportunities
  7. Antioxidant activity of phenolic extracts from different cultivars of Italian onion (Allium cepa) and relative human immune cell proliferative induction
  8. Diastereo- and enantioseparation of a Nα-Boc amino acid with a zwitterionic quinine-based stationary phase: Focus on the stereorecognition mechanism
  9. S-Trityl-(R)-Cysteine, a Multipurpose Chiral Selector for Ligand-Exchange Liquid Chromatography Applications
  10. ChemInform Abstract: Microwave-Assisted Cycloaddition of Diisopropyl Diazomethylphosphonate to Electron-Deficient Alkenes: Synthesis of Multifunctionalized Phosphonopyrazolines and Phosphonopyrazoles.
  11. N-Aryl-5-aminopyrazole: A Versatile Architecture in Medicinal Chemistry
  12. Microwave-assisted cycloaddition of diisopropyl diazomethylphosphonate to electron-deficient alkenes: synthesis of multifunctionalized phosphonopyrazolynes and phosphonopyrazoles
  13. Beyond Bile Acids: Targeting Farnesoid X Receptor (FXR) with Natural and Synthetic Ligands
  14. Editorial: (Thematic Issue: Medicinal Chemistry of Farnesoid X Receptor (FXR) Modulators: The-State-of-the-Art)
  15. ChemInform Abstract: One-Pot, Telescoped Synthesis of N-Aryl-5-aminopyrazoles from Anilines in Environmentally Benign Conditions.
  16. One-pot, telescoped synthesis of N-aryl-5-aminopyrazoles from anilines in environmentally benign conditions
  17. Determination of bile salt critical micellization concentration on the road to drug discovery
  18. Combined monodimensional chromatographic approaches to monitor the presence of d-amino acids in cheese
  19. The effect of mobile phase composition in the enantioseparation of pharmaceutically relevant compounds with polysaccharide-based stationary phases
  20. Asymmetric synthesis of the four diastereoisomers of a novel non-steroidal farnesoid X receptor (FXR) agonist: Role of the chirality on the biological activity
  21. Simultaneous diastereo- and enantioseparation of farnesoid X receptor (FXR) agonists with a quinine carbamate-based chiral stationary phase
  22. Pyrazole[3,4-e][1,4]thiazepin-7-one derivatives as a novel class of Farnesoid X Receptor (FXR) agonists
  23. Exploring the Synthetic Versatility of the Lewis Acid Induced Decomposition Reaction of α-Diazo-β-hydroxy Esters. The Case of Ethyl Diazo(3-hydroxy-2-oxo-2,3-dihydro-1H-indol-3-yl)acetate
  24. ChemInform Abstract: Metabotropic Glutamate Receptors: Structure and New Subtype-Selective Ligands
  25. ChemInform Abstract: Synthesis and Preliminary Biological Evaluation at the GlycineB Site of (+)- and (-)-3-Oxetanylglycine, Novel Non-proteinogenic Amino Acids.
  26. ChemInform Abstract: Design, Synthesis and Preliminary Evaluation of Novel 3′-Substituted Carboxycyclopropylglycines (XIV) as Antagonists at Group 2 Metabotropic Glutamate Receptors.
  27. Chiral ligand-exchange separation and resolution of extremely rigid glutamate analogs: 1-aminospiro[2.2]pentyl-1,4-dicarboxylic acids
  28. ChemInform Abstract: Exploring the Metal-Catalyzed Reactions of Furans with Alkyl α-Diazomethanesulfonate and α-Diazomethanephosphonate: Synthesis of ω-Acyl-Substituted Sulfono- and Phosphonobutadienes.
  29. Synthesis and chromatographic resolution of conformationally constrained analogues of homotaurine
  30. Exploring the metal-catalyzed reaction of furans with alkyl α-diazomethanesulfonate and α-diazomethanephosphonate: synthesis of ω-acyl-substituted sulfono- and phosphonobutadienes
  31. Design, synthesis and biological evaluation of novel bicyclo[1.1.1]pentane-based ω-acidic amino acids as glutamate receptors ligands
  32. Sequence Variants in Kynurenine Aminotransferase II (KAT II) Orthologs Determine Different Potencies of the InhibitorS-ESBA
  33. Synthesis, Molecular Modeling Studies, and Preliminary Pharmacological Characterization of All Possible 2-(2‘-Sulfonocyclopropyl)glycine Stereoisomers as Conformationally ConstrainedL-Homocysteic Acid Analogs
  34. Synthesis and biological evaluation of (2S)- and (2R)-2-(3′-phosphonobicyclo[1.1.1]pentyl)glycines as novel group III selective metabotropic glutamate receptor ligands
  35. Modulators of the Kynurenine Pathway of Tryptophan Metabolism: Synthesis and Preliminary Biological Evaluation of (S)-4-(Ethylsulfonyl)benzoylalanine, a Potent and Selective Kynurenine Aminotransferase II (KAT II) Inhibitor
  36. Cover Picture: Modulators of the Kynurenine Pathway of Tryptophan Metabolism: Synthesis and Preliminary Biological Evaluation of (S)-4-(Ethylsulfonyl)benzoylalanine, a Potent and Selective Kynurenine Aminotransferase II (KAT II) Inhibitor (ChemMedChem ...
  37. Synthesis and Preliminary Biological Evaluation of (2S,1′R,2′S)- and (2S,1′S,2′R)-2-(2′-Phosphonocyclopropyl)glycines, Two Novel Conformationally Constrained L-AP4 Analogues.
  38. Synthesis and Preliminary Biological Evaluation of 2′-Substituted 2-(3′-Carboxybicyclo[1.1.1]pentyl)glycine Derivatives as Group I Selective Metabotropic Glutamate Receptor Ligands
  39. Synthesis and preliminary biological evaluation of (2S,1′R,2′S)- and (2S,1′S,2′R)-2-(2′-phosphonocyclopropyl)glycines, two novel conformationally constrained l-AP4 analogues
  40. Conformationally constrained amino acids: enantiodivergent synthesis of all four stereoisomers of 2-(tetrahydrofuran-2-yl)glycine
  41. Synthesis of Novel Unsymmetrically Bridgehead-Substituted Phenylselenobicyclo[1.1.1]pentanes.
  42. Evaluation of the enantiomeric selectivity in the chiral ligand-exchange chromatography of amino acids by a computational model
  43. Stereoselective synthesis and preliminary evaluation of (+)- and (–)-3-methyl-5-carboxy-thien-2-yl-glycine (3-MATIDA): identification of (+)-3-MATIDA as a novel mGluR1 competitive antagonist
  44. Towards New Neuroprotective Agents: Design and Synthesis of 4H-Thieno[2,3-c]isoquinolin-5-one Derivatives as Potent PARP-1 Inhibitors.
  45. Preparative resolution of 1-aminoindan-1,5-dicarboxylic acid (AIDA) by chiral ligand-exchange chromatography
  46. Synthesis of Novel Unsymmetrically Bridgehead-substituted Phenylseleno­bicyclo[1.1.1]pentanes
  47. Towards new neuroprotective agents: design and synthesis of 4H-thieno[2,3-c] isoquinolin-5-one derivatives as potent PARP-1 inhibitors
  48. Thermal and Catalytic Reaction of Diazoacetylmetallocenes with [60]Fullerene.
  49. Heterocycles as Companions on Route to Drug Discovery
  50. Thermal and Catalytic Reactions of Diazoacetylmetallocenes with [60]Fullerene
  51. Spiro[2.2]pentane as a Dissymmetric Scaffold for Conformationally Constrained Analogues of Glutamic Acid:  Focus on Racemic 1-Aminospiro[2.2]pentyl-1,4-dicarboxylic Acids
  52. Design, synthesis and preliminary evaluation of novel 3′-Substituted carboxycyclopropylglycines as antagonists at group 2 metabotropic glutamate receptors
  53. Synthesis and preliminary biological evaluation at the glycineB site of (+)- and (−)-3-oxetanylglycine, novel non-proteinogenic amino acids
  54. ChemInform Abstract: Synthesis of Methano[60]fullerenephosphonic- and Methano[60]fullerene-diphosphonic Acids.
  55. Metabotropic glutamate receptors: structure and new subtype-selective ligands
  56. Synthesis and biological evaluation of 2-(3′-(1 H -tetrazol-5-yl)bicyclo[1.1.1]pent-1-yl)glycine ( S -TBPG), a novel mGlu1 receptor antagonist
  57. Novel enantioselective synthesis of (2S,2′R,3′R)-2-(2′,3′-dicarboxycyclopropyl)glycine (DCG-IV)
  58. ChemInform Abstract: Synthesis, Molecular Modeling and Preliminary Biological Evaluation of 1-Amino-3-phosphono-3-cyclopentene-1-carboxylic Acid and 1-Amino-3-phosphono-2-cyclopentene-1-carboxylic Acid, Two Novel Agonists of Metabotropic Glutamate Recepto
  59. Modulation of glutamate receptor pathways in the search for new neuroprotective agents
  60. Dirhodium(II) Tetraacetate-Mediated Decomposition of Ethyldiazoacetate and Ethyldiazomalonate in the Presence of Fullerene. A New Procedure for the Selective Synthesis of [6-6]-Closed Methanofullerenes
  61. Asymmetric synthesis of enantiomerically pure (2S,1′S,2′S,3′R)-phenylcarboxycyclopropylglycine (PCCG-4): a potent and selective ligand at group II metabotropic glutamate receptors
  62. (S)-(+)-2-(3‘-Carboxybicyclo[1.1.1]pentyl)- glycine, a Structurally New Group I Metabotropic Glutamate Receptor Antagonist
  63. 1-Aminoindan-1,5-dicarboxylic Acid: A Novel Antagonist at Phospholipase C-Linked Metabotropic Glutamate Receptors
  64. NMDA receptor heterogeneity in mammalian tissues: focus on two agonists, (2S,3R,4S) cyclopropylglutamate and the sulfate ester of 4-hydroxy-(S)-pipecolic acid
  65. Synthesis of all four diastereoisomers of 4-(carboxymethyl)proline, a conformationally constrained analogue of 2-aminoadipic acid
  66. Synthesis of 2-azabicyclo[3.1.0]hexane tricarboxylate and its transformation into a new proline-γ-acetic acid equivalent
  67. Sulfate esters of hydroxy amino acids as stereospecific glutamate receptor agonists
  68. Brush-border-enzyme-mediated intestine-specific drug delivery. Amino acid prodrugs of 5-aminosalicylic acid
  69. D-3,4-‘cyclopropylglutamate’ isomers as nmda receptor ligands: Synthesis and enantioselective activity.
  70. Preparation and physicochemical properties of natural (23R)-3α,7α,23- and (23R)-3α,12α,23-trihydroxylated bile acids and their (23S)-epimers
  71. L-Vinylglycine from L-Homoserine.
  72. L-α-Aminoadipic Acid from L-Glutamic Acid