135 results on '"Di Braccio, Mario"'
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2. 1,8-Naphthyridines IX. Potent anti-inflammatory and/or analgesic activity of a new group of substituted 5-amino[1,2,4]triazolo[4,3-a][1,8]naphthyridine-6-carboxamides, of some their Mannich base derivatives and of one novel substituted 5-amino-10-oxo-10H-pyrimido[1,2-a][1,8]naphthyridine-6-carboxamide derivative
3. Anticonvulsive Activity in Audiogenic DBA/2 Mice of 1,4-Benzodiazepines and 1,5-Benzodiazepines with Different Activities at Cerebellar Granule Cell GABAA Receptors
4. Fine molecular tuning at position 4 of 2H-chromen-2-one derivatives in the search of potent and selective monoamine oxidase B inhibitors
5. Synthesis, in vitro antiplatelet activity and molecular modelling studies of 10-substituted 2-(1-piperazinyl)pyrimido[1,2-a]benzimidazol-4(10H)-ones
6. Study of the Interaction of 1,4- and 1,5-Benzodiazepines with GABAA Receptors of Rat Cerebellum Granule Cells in Culture
7. GABAA Receptors of Cerebellar Granule Cells in Culture: Interaction with Benzodiazepines
8. 1,8-Naphthyridines VII. New substituted 5-amino[1,2,4]triazolo[4,3- a][1,8]naphthyridine-6-carboxamides and their isosteric analogues, exhibiting notable anti-inflammatory and/or analgesic activities, but no acute gastrolesivity
9. 1,8-Naphthyridines VI. Synthesis and anti-inflammatory activity of 5-(alkylamino)- N, N-diethyl[1,2,4]triazolo[4,3- a][1,8]naphthyridine-6-carboxamides with a new substitution pattern on the triazole ring
10. 1,8-Naphthyridines V. Novel N-substituted 5-amino- N, N-diethyl-9-isopropyl [1,2,4]triazolo[4,3- a] [1,8]naphthyridine-6-carboxamides, as potent anti-inflammatory and/or analgesic agents completely devoid of acute gastrolesivity
11. Synthesis and in vitro inhibitory activity on human platelet aggregation of novel properly substituted 4-(1-piperazinyl)coumarins
12. 1,5-Benzodiazepines: Part XIII. Substituted 4 H-[1,2,4]triazolo[4,3- a][1,5]benzodiazepin-5-amines and 4 H-imidazo[1,2- a][1,5]benzodiazepin-5-amines as analgesic, anti-inflammatory and/or antipyretic agents with low acute toxicity
13. Effects of anti-inflammatory [1, 2, 4]triazolo[4, 3-a] [1, 8]naphthyridine derivatives on human stimulated PMN and endothelial cells: an in vitro study
14. 1,5-Benzodiazepine tricyclic derivatives exerting anti-inflammatory effects in mice by inhibiting interleukin-6 and prostaglandinE2production
15. Modulation of GABAA by Clobazam and Diazepam in the presence of Furosemide and Zn2+
16. Crystal structure of N,N'-dimethyl-1-phenyl-4H-[1,2,4]triazolo[4,3-a][1,5]-benzodiazepin-5-amine,C18H17N5
17. Effects of anti-inflammatory[1,2,4]triazolo[4.3-a]naphthyridine derivatives on human stimulated PMN and endothelial cells: an in vitro study
18. Synthesis, antiplatelet activity and comparative molecular fields analysis of substituted 2-amino-4H-pyrido[1,2-a]pyrimidin-4-ones, their congeners and isosteric analogues
19. Synthesis, in vitro antiplatelet activity and molecular modelling studies of 10-substituted 2-(1-piperazinyl)pyrimido[1,2- a ]benzimidazol-4(10 H )-ones
20. ChemInform Abstract: Pyran Derivatives. Part 20. 2-Aminochromone Benzo-Fused Derivatives with Antiproliferative Properties.
21. ChemInform Abstract: Efficient One‐Pot Synthesis of N‐Substituted 2‐Aminochromones, Their Benzo‐Fused Derivatives, and Diaminobenzodipyrandiones of Two New Structural Classes.
22. ChemInform Abstract: 1,5-Benzodiazepines. Part 12. Synthesis and Biological Evaluation of Tricyclic and Tetracyclic 1,5-Benzodiazepine Derivatives as Nevirapine Analogues.
23. ChemInform Abstract: 1,8‐Naphthyridines. Part 8. Novel 5‐Aminoimidazo[1,2‐a][1,8]naphthyridine‐6‐carboxamide and 5‐Amino[1,2,4]triazolo[4,3‐a][1,8]naphthyridine‐6‐carboxamide Derivatives Showing Potent Analgesic or Antiinflammatory Activity, Respectively, and Completely Devoid of Acute Gastrolesivity.
24. Efficient One-Pot Synthesis of N-Substituted 2-Aminochromones, Their Benzo-Fused Derivatives, and Diaminobenzodipyrandiones of Two New Structural Classes
25. 1,8-Naphthyridines VIII. Novel 5-aminoimidazo[1,2-a] [1,8]naphthyridine-6-carboxamide and 5-amino[1,2,4]triazolo[4,3-a] [1,8]naphthyridine-6-carboxamide derivatives showing potent analgesic or anti-inflammatory activity, respectively, and completely devoid of acute gastrolesivity
26. ChemInform Abstract: 1,8‐Naphthyridines. Part 6. Synthesis and Antiinflammatory Activity of 5‐(Alkylamino)‐N,N‐diethyl[1,2,4]triazolo[4,3‐a] [1,8]naphthyridine‐6‐carboxamides with a New Substitution Pattern on the Triazole Ring.
27. 1,8-Naphthyridines VI. Synthesis and anti-inflammatory activity of 5-(alkylamino)-N,N-diethyl[1,2,4]triazolo[4,3-a][1,8]naphthyridine-6-carboxamides with a new substitution pattern on the triazole ring
28. Synthesis and In Vitro Antiplatelet Activity of New 4-(1-Piperazinyl)coumarin Derivatives. Human Platelet Phosphodiesterase 3 Inhibitory Properties of the Two Most Effective Compounds Described and Molecular Modeling Study on Their Interactions with Phosphodiesterase 3A Catalytic Site
29. Effects of anti-inflammatory [1, 2, 4]triazolo[4, 3-a] [1, 8]naphthyridine derivatives on human stimulated PMN and endothelial cells: an in vitro study
30. 1,5-Benzodiazepines. Part 14. Synthesis of New Substituted 9H-Bis-[1,2,4]triazolo[4,3-a:3′,4′.d][1,5]benzodiazepines and Related Compounds Endowed with in vitro Cytotoxic Properties.
31. 1,8-Naphthyridines. Part 5. Novel N-Substituted 5-Amino-N,N-diethyl-9-isopropyl[1,2,4]triazolo[4,3-a] [1,8]naphthyridine-6-carboxamides, as Potent Antiinflammatory and/or Analgesic Agents Completely Devoid of Acute Gastrolesivity.
32. 1,8-Naphthyridines V. Novel N-substituted 5-amino-N,N-diethyl-9-isopropyl [1,2,4]triazolo[4,3-a] [1,8]naphthyridine-6-carboxamides, as potent anti-inflammatory and/or analgesic agents completely devoid of acute gastrolesivity
33. 1,5-Benzodiazepines XIV. Synthesis of new substituted 9H-bis-[1,2,4]triazolo[4,3-a:3′,4′-d] [1,5]benzodiazepines and relate compounds endowed with in vitro cytotoxic properties
34. Synthesis and in vitro Inhibitory Activity on Human Platelet Aggregation of Novel Properly Substituted 4‐(1‐Piperazinyl)coumarins.
35. Pyran Derivatives. Part 21. Antiproliferative and Cytotoxic Properties of Novel N-Substituted 4-Aminocoumarins, Their Benzo-Fused Derivatives, and Some Related 2-Aminochromones.
36. Pyran derivatives
37. 1,5-Benzodiazepines. Part 13. Substituted 4H-[1,2,4]Triazolo[4,3-a][1,5]benzodiazepin-5-amines and 4H-Imidazo[1,2-a][1,5]benzodiazepin-5-amines as Analgesic, Antiinflammatory and/or Antipyretic Agents with Low Acute Toxicity.
38. Coumarin, Chromone, and 4(3H)‐Pyrimidinone Novel Bicyclic and Tricyclic Derivatives as Antiplatelet Agents: Synthesis, Biological Evaluation, and Comparative Molecular Field Analysis.
39. 1,5-Benzodiazepines. Part XII. Synthesis and biological evaluation of tricyclic and tetracyclic 1,5-benzodiazepine derivatives as nevirapine analogues
40. ChemInform Abstract: 1,8‐Naphthyridines. Part 4. 9‐Substituted N,N‐Dialkyl‐5‐(alkylamino or cycloalkylamino) [1,2,4]Triazolo[4,3‐a][1,8]naphthyridine‐6‐carboxamides, New Compounds with Antiaggressive and Potent Antiinflammatory Activities.
41. 1,8-Naphthyridines IV. 9-Substituted N,N-dialkyl-5-(alkylamino or cycloalkylamino) [1,2,4]triazolo[4,3-a][1,8]naphthyridine-6-carboxamides, new compounds with anti-aggressive and potent anti-inflammatory activities
42. Synthesis, antiplatelet activity and comparative molecular field analysis of substituted 2-amino-4 H -pyrido[1,2- a ]pyrimidin-4-ones, their congeners and isosteric analogues
43. Pyran derivatives XX. 2-Aminochromone benzo-fused derivatives with antiproliferative properties
44. MECHANISM OF ACTION OF TWO NEW PYRIMIDOQUINOLINE AND ISOQUINOLINE DERIVATIVES IN HUMAN PLATELETS
45. GABAA Receptors of Cerebellar Granule Cells in Culture: Interaction with Benzodiazepines.
46. 1,2‐fused pyrimidines. V. Synthesis of 1‐alkyl or phenyl‐2H‐dipyrido‐[1,2‐a:2′,3′‐d]pyrimidine‐2,5(1H)‐diones
47. Pyran derivatives: Part XXI. Antiproliferative and cytotoxic properties of novel N-substituted 4-aminocoumarins, their benzo-fused derivatives, and some related 2-aminochromones
48. 1,2-fused pyrimidines. V. Synthesis of 1-alkyl or phenyl-2 H-dipyrido-[1,2- a:2′,3′- d]pyrimidine-2,5(1 H)-diones.
49. Naphtho[1′,2′:5,6]pyrano[2,3-6][1,5]benzodiazepine Derivatives.
50. 1,8-Naphthyridines IV. 9-Substituted N, N-dialkyl-5-(alkylamino or cycloalkylamino) [1,2,4]triazolo[4,3- a][1,8]naphthyridine-6-carboxamides, new compounds with anti-aggressive and potent anti-inflammatory activities
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