All Stories

  1. Chemical and biological insights into 3-arylphenytoins as urease inhibitors: Design, synthesis, in vitro and in silico studies
  2. In vitro and In silico Xanthine Oxidase Inhibitory Activities of 3-Aryl-2- thioxo-2,3-dihydroquinazolin-4(1H)-one Derivatives
  3. New synthetic phenylquinazoline derivatives induce apoptosis by targeting the pro-survival members of the BCL-2 family
  4. Potential anti-acanthamoebic effects through inhibition of CYP51 by novel quinazolinones
  5. Biology‐oriented drug synthesis and evaluation of secnidazole esters as novel enzyme ınhibitors
  6. An effort to find new α-amylase inhibitors as potent antidiabetics compounds based on indole-based-thiadiazole analogs
  7. Antioxidant and ROS Inhibitory Activities of Heterocyclic 2-Aryl-4(3H)-quinazolinone Derivatives
  8. Rapid Cesium Fluoride Catalyzed Synthesis of 5-Aryloxy-1-phenyl-1H-tetrazoles via Nucleophilic Aromatic Substitution
  9. Antiamoebic activity of 3-aryl-6,7-dimethoxyquinazolin-4(3H)-one library against Acanthamoeba castellanii
  10. Thymidine phosphorylase and prostrate cancer cell proliferation inhibitory activities of synthetic 4-hydroxybenzohydrazides: In vitro, kinetic, and in silico studies
  11. Aryl Quinazolinone Derivatives as Novel Therapeutic Agents against Brain-Eating Amoebae
  12. Facile CuCl2·2H2O catalyzed one-pot conversion of dimedone into highly functionalized indazole based N-arylhydrazinecarbothioamides
  13. Novel antiacanthamoebic compounds belonging to quinazolinones
  14. Synthesis, molecular docking and xanthine oxidase inhibitory activity of 5-aryl-1H-tetrazoles
  15. Coumarin sulfonates: As potential leads for ROS inhibition
  16. Synthesis and urease inhibitory activities of benzophenone semicarbazones/thiosemicarbazones
  17. Synthesis, molecular docking and α-glucosidase inhibition of 5-aryl-2-(6′-nitrobenzofuran-2′-yl)-1,3,4-oxadiazoles
  18. Microwave-assisted green approach toward the unexpected synthesis of pyrazole-4-carboxylates
  19. Synthesis, α-glucosidase inhibitory, cytotoxicity and docking studies of 2-aryl-7-methylbenzimidazoles
  20. An efficient one-pot protocol for the conversion of benzaldehydes into tetrazole analogs
  21. 2-Arylquinazolin-4(3H)-ones: Inhibitory Activities Against Xanthine Oxidase
  22. 4-Arylamino-6-nitroquinazolines: Synthesis and their activities against neglected disease leishmaniasis
  23. Evaluation of 2-indolcarbohydrazones as potent α-glucosidase inhibitors, in silico studies and DFT based stereochemical predictions
  24. 2-Arylquinazolin-4(3H)-ones: A new class of α-glucosidase inhibitors
  25. 2-Arylquinazolin-4(3H)-ones: A novel class of thymidine phosphorylase inhibitors
  26. Corrigendum to “2-Arylquinazolin-4(3H)-ones: A new class of α-glucosidase inhibitors” [Bioorg. Med. Chem. 23 (2015) 7417–7421]
  27. Synthesis of new oxadiazole derivatives as α-glucosidase inhibitors
  28. Synthesis and Biological Potential Assessment of 2-Substituted Quinazolin-4(3H)-ones as Inhibitors of Phosphodiesterase-I and Carbonic Anhydrase-II
  29. A new and facile CuCl2·2H2O-catalyzed one-pot three-component synthesis for quinazolines
  30. Synthesis of phenyl thiazole hydrazones and their activity against glycation of proteins
  31. Synthesis of triazole Schiff bases: Novel inhibitors of nucleotide pyrophosphatase/phosphodiesterase-1
  32. β-Glucuronidase Inhibitory Studies on Coumarin Derivatives
  33. Oxadiazoles and thiadiazoles: Novel α-glucosidase inhibitors
  34. WITHDRAWN: 2-Arylquinazolin-4(3H)-ones: A new class of α-glucosidase inhibitors
  35. Synthesis and β-glucuronidase inhibitory activity of 2-arylquinazolin-4(3H)-ones
  36. 2-{[(Dimethylamino)methylidene]amino}-5-nitrobenzonitrile
  37. N-(2,5-Dimethoxyphenyl)-6-nitroquinazolin-4-amine
  38. N′-(3-Chlorobenzylidene)-4-hydroxybenzohydrazide
  39. Ethyl (E)-3-(6-methyl-4-oxo-4H-chromen-3-yl)prop-2-enoate
  40. 6-Methyl-4-oxo-4H-chromene-3-carbaldehyde