All Stories

  1. Synthesis, characterization, and anticancer activity of Schiff bases
  2. Carbonic Anhydrase Inhibitory Potential of 1,2,4-triazole-3-thione Derivatives of Flurbiprofen, Ibuprofen and 4-tert-butylbenzoic Hydrazide: Design, Synthesis, Characterization, Biochemical Evaluation, Molecular Docking and Dynamic Simulation Studies
  3. Identification of New Chromenone Derivatives as Cholinesterase Inhibitors and Molecular Docking Studies
  4. Quinolinic Carboxylic Acid Derivatives as Potential Multi-target Compounds for Neurodegeneration: Monoamine Oxidase and Cholinesterase Inhibition
  5. Synthesis, Characterization and Cholinesterase Inhibition Studies of New Arylidene Aminothiazolylethanone Derivatives
  6. Synthesis, Characterization and Biological Activities of Creatinine Amides and Creatinine Schiff Bases
  7. Biological Evaluation of Azomethine-dihydroquinazolinone Conjugates as Cancer and Cholinesterase Inhibitors
  8. Quinolinyl-Thienyl Chalcones as Monoamine Oxidase Inhibitors and their In Silico Modeling Studies
  9. Biological Evaluation of Halogenated Thioureas as Cholinesterases Inhibitors Against Alzheimer’s Disease & Molecular Modeling Studies
  10. Investigation of quinoline-4-carboxylic acid as a highly potent scaffold for the development of alkaline phosphatase inhibitors: synthesis, SAR analysis and molecular modelling studies
  11. Synthesis, characterization and biological evaluation of N-(2,3-dimethyl-5-oxo-1-phenyl-2,5-dihydro-1H-pyrazol-4-yl)benzamides
  12. Facile and expedient access to bis-coumarin–iminothiazole hybrids by molecular hybridization approach: synthesis, molecular modelling and assessment of alkaline phosphatase inhibition, anticancer and antileishmanial potential
  13. Influence of the diversified structural variations at the imine functionality of 4-bromophenylacetic acid derived hydrazones on alkaline phosphatase inhibition: synthesis and molecular modelling studies
  14. Synthesis of chitosan-coated polyoxometalate nanoparticles against cancer and its metastasis
  15. Active compounds from a diverse library of triazolothiadiazole and triazolothiadiazine scaffolds: Synthesis, crystal structure determination, cytotoxicity, cholinesterase inhibitory activity, and binding mode analysis
  16. ChemInform Abstract: A Novel Example of Double 6-exo-trig Heterocyclization: Nitrile Conversion to New Anticancer Active (HeLa Cells) Primary Amine Ionic Liquids.
  17. 2‐(Hetero(aryl)methylene)hydrazine‐1‐carbothioamides as Potent Urease Inhibitors
  18. RutheniumII(η6-arene) Complexes of Thiourea Derivatives: Synthesis, Characterization and Urease Inhibition
  19. A Facile One‐Pot Synthesis of 2‐Arylamino‐5‐Aryloxylalkyl‐1,3,4‐Oxadiazoles and Their Urease Inhibition Studies
  20. New aminobenzenesulfonamide–thiourea conjugates: Synthesis and carbonic anhydrase inhibition and docking studies
  21. Novel structural hybrids of pyrazolobenzothiazines with benzimidazoles as cholinesterase inhibitors
  22. Synthesis, crystal structure and biological evaluation of some novel 1,2,4-triazolo[3,4-b]-1,3,4-thiadiazoles and 1,2,4-triazolo[3,4-b]-1,3,4-thiadiazines
  23. Synthesis, cytotoxicity and molecular modelling studies of new phenylcinnamide derivatives as potent inhibitors of cholinesterases
  24. ChemInform Abstract: Solution‐Phase Microwave Assisted Parallel Synthesis of N,N′‐Disubstituted Thioureas Derived from Benzoic Acid: Biological Evaluation and Molecular Docking Studies.
  25. Carbonic anhydrase inhibition by 1-aroyl-3-(4-aminosulfonylphenyl)thioureas
  26. Design, synthesis, molecular docking studies and in vitro screening of ethyl 4-(3-benzoylthioureido) benzoates as urease inhibitors
  27. A novel example of double 6-exo-trig heterocyclization: nitrile conversion to new anticancer active (HeLa cells) primary amine ionic liquids
  28. Synthesis and antiproliferative activity of (Z)-1-glycosyl-3-(5-oxo-2-thioxoimidazolidin-4-ylidene)indolin-2-ones and (Z)-3-(2-glycosylsulfanyl-4-oxo-4,5-dihydro-thiazol-5-ylidene)indolin-2-ones
  29. Synthesis and antiproliferative activity of N-glycosyl-3,3-diaryloxindoles
  30. Antidiabetic potential of polyoxotungstates: in vitro and in vivo studies
  31. Benzothiazolyl substituted iminothiazolidinones and benzamido-oxothiazolidines as potent and partly selective aldose reductase inhibitors
  32. A capillary electrophoresis-based enzyme assay for kinetics and inhibition studies of carbonic anhydrase
  33. Sulfa Drugs as Inhibitors of Carbonic Anhydrase: New Targets for the Old Drugs
  34. Cytotoxicity and enzyme inhibition studies of polyoxometalates and their chitosan nanoassemblies
  35. Solution-phase microwave assisted parallel synthesis of N,N′-disubstituted thioureas derived from benzoic acid: Biological evaluation and molecular docking studies
  36. Identification of sulfonic acids as efficient ecto-5′-nucleotidase inhibitors
  37. Development of a fast and efficient CE enzyme assay for the characterization and inhibition studies of α-glucosidase inhibitors
  38. Therapeutic Potentials of Ecto‐Nucleoside Triphosphate Diphosphohydrolase, Ecto‐Nucleotide Pyrophosphatase/Phosphodiesterase, Ecto‐5′‐Nucleotidase, and Alkaline Phosphatase Inhibitors
  39. Synthesis of BODIPY Derivatives Substituted with Various Bioconjugatable Linker Groups: A Construction Kit for Fluorescent Labeling of Receptor Ligands
  40. Identification of novel chromone based sulfonamides as highly potent and selective inhibitors of alkaline phosphatases
  41. ChemInform Abstract: Synthesis of Functionalized Benzothiophenes and Dibenzothiophenes by Twofold Heck and Subsequent 6π‐Electrocyclization Reactions of 2,3‐Dibromothiophenes and 2,3‐Dibromobenzothiophenes.
  42. ChemInform Abstract: Synthesis of 2,6‐Diaryl‐3‐(trifluoromethyl)pyridines by Regioselective Suzuki—Miyaura Reactions of 2,6‐Dichloro‐3‐(trifluoromethyl)pyridine.
  43. ChemInform Abstract: Synthesis and Photophysical Properties of Tetra‐ and Pentaalkynylfluorobenzenes by Sonogashira Reactions of Novel Iodofluorobenzenes.
  44. ChemInform Abstract: Synthesis of Functionalized Fluorinated Terphenyls by Site‐Selective Suzuki—Miyaura Cross‐Coupling Reactions of Dibrominated Fluorobenzenes.
  45. ChemInform Abstract: Pyrrole versus Quinoline Formation in the Palladium Catalyzed Reaction of 2‐Alkynyl‐3‐bromothiophenes and 2‐Alkynyl‐3‐bromofurans with Anilines. A Combined Experimental and Computational Study.
  46. Synthesis of 2,6-diaryl-3-(trifluoromethyl)pyridines by regioselective Suzuki–Miyaura reactions of 2,6-dichloro-3-(trifluoromethyl)pyridine
  47. Synthesis of functionalized fluorinated terphenyls by site-selective Suzuki–Miyaura cross-coupling reactions of dibrominated fluorobenzenes
  48. Advances in immobilized enzyme microbioreactors in capillary electrophoresis
  49. Synthesis and antiproliferative activity of selenoindirubins and selenoindirubin-N-glycosides
  50. Synthesis of N,N′-diglycosylated isoindigos
  51. Synthesis, crystal structure, enzyme inhibition, DNA protection, and antimicrobial studies of di- and triorganotin(IV) derivatives of 2-thiopheneacetic acid
  52. Synthesis and photophysical properties of tetra- and pentaalkynylfluorobenzenes by Sonogashira reactions of novel iodofluorobenzenes
  53. Dual action spirobicycloimidazolidine-2,4-diones: Antidiabetic agents and inhibitors of aldose reductase-an enzyme involved in diabetic complications
  54. Synthesis of functionalized benzothiophenes and dibenzothiophenes by twofold Heck and subsequent 6π-electrocyclization reactions of 2,3-dibromothiophenes and 2,3-dibromobenzothiophenes
  55. Structural, enzyme inhibition, antibacterial and DNA protection studies of organotin(IV) derivatives of thiophene-2-carboxylic acid
  56. Synthesis of trifluoromethyl-substituted bi- and terphenyls by site-selective Suzuki–Miyaura reactions of various dihalogenated trifluoromethyl-benzene derivatives
  57. Synthesis, molecular docking studies, and in vitro screening of sulfanilamide-thiourea hybrids as antimicrobial and urease inhibitors
  58. Identification of Small Molecule Sulfonic Acids as Ecto-5'-Nucleotidase Inhibitors
  59. Identification of Small Molecule Sulfonic Acids as Ecto-5'-Nucleotidase Inhibitors
  60. Pharmacological Evaluation and Docking Studies of 3-Thiadiazolyl- and Thioxo-1,2,4-triazolylcoumarin Derivatives as Cholinesterase Inhibitors
  61. Synthesis, Urease Inhibition, Antioxidant, Antibacterial, and Molecular Docking Studies of 1,3,4-Oxadiazole Derivatives
  62. Synthesis and Biological Evaluation of 3‐thiazolocoumarinyl Schiff‐base Derivatives as Cholinesterase Inhibitors
  63. Antioxidant, Antimicrobial, and Free Radical Scavenging Potential of Aerial Parts of Periploca aphylla and Ricinus communis
  64. Polyoxometalates as potent inhibitors for acetyl and butyrylcholinesterases and as potential drugs for the treatment of Alzheimer’s disease
  65. Synthesis, urease inhibition, antioxidant and antibacterial studies of some 4-amino-5-aryl-3H-1,2,4-triazole-3-thiones and their 3,6-disubstituted 1,2,4-triazolo[3,4-b]1,3,4-thiadiazole derivatives
  66. Benzothiazinones: A Novel Class of Adenosine Receptor Antagonists Structurally Unrelated to Xanthine and Adenine Derivatives
  67. Polyoxometalates as potent and selective inhibitors of alkaline phosphatases with profound anticancer and amoebicidal activities
  68. Design, synthesis and molecular modelling of novel methyl[4-oxo-2-(aroylimino)-3-(substituted phenyl)thiazolidin-5-ylidene]acetates as potent and selective aldose reductase inhibitors
  69. Pyrrole versus quinoline formation in the palladium catalyzed reaction of 2-alkynyl-3-bromothiophenes and 2-alkynyl-3-bromofurans with anilines. A combined experimental and computational study
  70. Synthesis, Acetylcholinesterase and Alkaline Phosphatase Inhibition of Some New 1,2,4-Triazole and 1,3,4-Thiadiazole Derivatives
  71. Synthesis, biological assay in vitro and molecular docking studies of new Schiff base derivatives as potential urease inhibitors
  72. Identification of Potent and Selective Human Ecto-Nucleotide Pyrophosphatase/ Phosphodiesterase-3 (hNPP3) Inhibitors
  73. An enzyme immobilized microassay in capillary electrophoresis for characterization and inhibition studies of alkaline phosphatases
  74. High-sensitivity capillary electrophoresis method for monitoring purine nucleoside phosphorylase and adenosine deaminase reactions by a reversed electrode polarity switching mode
  75. Development of Potent and Selective Inhibitors of ecto-5′-Nucleotidase Based on an Anthraquinone Scaffold
  76. Development of a microbioreactor with ecto-nucleoside triphosphate diphosphohydrolase 2 (NTPDase2) immobilized on a polyacrylamide-coated capillary at the outlet
  77. Nucleoside-5′-monophosphates as Prodrugs of Adenosine A2A Receptor Agonists Activated by ecto-5′-Nucleotidase†Contribution to celebrate the 100th anniversary of the Division of Medicinal Chemistry of the American Chemical Society.
  78. Tether tracking and control of ROSA robotic rover
  79. A highly sensitive CE‐UV method with dynamic coating of silica‐fused capillaries for monitoring of nucleotide pyrophosphatase/phosphodiesterase reactions
  80. Selective Nucleoside Triphosphate Diphosphohydrolase-2 (NTPDase2) Inhibitors: Nucleotide Mimetics Derived from Uridine-5′-carboxamide
  81. Structure-activity relationships of anthraquinone derivatives derived from bromaminic acid as inhibitors of ectonucleoside triphosphate diphosphohydrolases (E-NTPDases)
  82. Capillary electrophoresis-based nanoscale assays for monitoring ecto-5′-nucleotidase activity and inhibition in preparations of recombinant enzyme and melanoma cell membranes
  83. Polyoxometalates—a new class of potent ecto-nucleoside triphosphate diphosphohydrolase (NTPDase) inhibitors
  84. Characterization of human and rodent native and recombinant adenosine A2B receptors by radioligand binding studies
  85. Development of off‐line and on‐line capillary electrophoresis methods for the screening and characterization of adenosine kinase inhibitors and substrates
  86. A capillary electrophoresis method for the characterization of ecto-nucleoside triphosphate diphosphohydrolases (NTPDases) and the analysis of inhibitors by in-capillary enzymatic microreaction
  87. Novel Amino Acid Derived Natural Products from the Ascidian Atriolum robustum: Identification and Pharmacological Characterization of a Unique Adenosine Derivative (IIIa).
  88. Novel Amino Acid Derived Natural Products from the Ascidian Atriolum robustum:  Identification and Pharmacological Characterization of a Unique Adenosine Derivative