549 results on '"Barraja, Paola"'
Search Results
2. Identification of 6,9-dihydro-5H-pyrrolo[3,2-h]quinazolines as a new class of F508del-CFTR correctors for the treatment of cystic fibrosis
3. Novel tricyclic pyrrolo-quinolines as pharmacological correctors of the mutant CFTR chloride channel
4. Advances in developing noncovalent small molecules targeting Keap1
5. Identification of pyrrolo[3′,4’:3,4]cyclohepta[1,2-d][1,2]oxazoles as promising new candidates for the treatment of lymphomas
6. Exploring the anticancer activity and the mechanism of action of pyrrolomycins F obtained by microwave-assisted total synthesis
7. Insight into non-nucleoside triazole-based systems as viral polymerases inhibitors
8. New tricyclic systems as photosensitizers towards triple negative breast cancer cells
9. Development of [1,2]oxazoloisoindoles tubulin polymerization inhibitors: Further chemical modifications and potential therapeutic effects against lymphomas
10. Insight on pyrimido[5,4-g]indolizine and pyrimido[4,5-c]pyrrolo[1,2-a]azepine systems as promising photosensitizers on malignant cells
11. Synthesis of 2H-Imidazo[2′,1':2,3] [1,3]thiazolo[4,5-e]isoindol-8-yl-phenylureas with promising therapeutic features for the treatment of acute myeloid leukemia (AML) with FLT3/ITD mutations
12. New strategies to hit hematological cancers
13. Recurrence of the oxazole motif in tubulin colchicine site inhibitors with anti-tumor activity
14. Insight on [1,3]thiazolo[4,5-e]isoindoles as tubulin polymerization inhibitors
15. Bioactive pyrrole-based compounds with target selectivity
16. Current development of CFTR potentiators in the last decade
17. Pyrrolidine in Drug Discovery: A Versatile Scaffold for Novel Biologically Active Compounds
18. Targeting multiple myeloma with natural polyphenols
19. An overview on chemical structures as ΔF508-CFTR correctors
20. Furocoumarins as multi-target agents in the treatment of cystic fibrosis
21. Synthesis and photocytotoxic activity of [1,2,3]triazolo[4,5-h][1,6]naphthyridines and [1,3]oxazolo[5,4-h][1,6]naphthyridines
22. Synthesis of 5H-pyrido[3,2-b]pyrrolizin-5-one tripentone analogs with antitumor activity
23. 1,3,5-Triazines: A promising scaffold for anticancer drugs development
24. An overview on the recent developments of 1,2,4-triazine derivatives as anticancer compounds
25. Synthesis and antitumor activities of 1,2,3-triazines and their benzo- and heterofused derivatives
26. Synthesis, antitumor activity and CDK1 inhibiton of new thiazole nortopsentin analogues
27. Pyrrolo[3′,2′:6,7]cyclohepta[1,2-b]pyridines with potent photo-antiproliferative activity
28. HSV-1 Glycoprotein D and Its Surface Receptors: Evaluation of Protein–Protein Interaction and Targeting by Triazole-Based Compounds through In Silico Approaches
29. [1,2]Oxazolo[5,4-e]isoindoles as promising tubulin polymerization inhibitors
30. Synthesis and antiproliferative mechanism of action of pyrrolo[3′,2′:6,7] cyclohepta[1,2-d]pyrimidin-2-amines as singlet oxygen photosensitizers
31. Synthesis of isoindolo[1,4]benzoxazinone and isoindolo[1,5]benzoxazepine: two new ring systems of pharmaceutical interest
32. Pyrazolo[3,4-h]quinolines promising photosensitizing agents in the treatment of cancer
33. Aza-isoindolo and isoindolo-azaquinoxaline derivatives with antiproliferative activity
34. Water-soluble isoindolo[2,1-a]quinoxalin-6-imines: In vitro antiproliferative activity and molecular mechanism(s) of action
35. Antibody-drug conjugates for lymphoma patients: preclinical and clinical evidences
36. The New Microtubule-Targeting Agent SIX2G Induces Immunogenic Cell Death in Multiple Myeloma
37. ‘Interrupted’ diazotization of 3-aminoindoles and 3-aminopyrroles
38. Synthesis of a new class of pyrrolo[3,4-h]quinazolines with antimitotic activity
39. Novel insights on [1,2]oxazolo[5,4‐e]isoindoles on multidrug resistant acute myeloid leukemia cell line
40. Convenient synthesis of pyrrolo[3,4-g]indazole
41. Synthesis of [1,2]oxazolo[5,4-e]indazoles as antitumour agents
42. Synthesis of the new oligopeptide pyrrole derivative isonetropsin and its one pyrrole unit analogue
43. Marine anticancer agents: an overview with a particular focus on their chemical classes
44. An efficient synthesis of pyrrolo[3′,2′:4,5]thiopyrano[3,2-b]pyridin-2-one: a new ring system of pharmaceutical interest
45. Pyrrolo[3,4- h]quinolinones a new class of photochemotherapeutic agents
46. Synthesis of the new ring system pyrrolizino[2,3- b]indol-4(5 H)-one
47. GPCR Inhibition in Treating Lymphoma
48. Synthesis of pyrrolo[3,2- h]quinolinones with good photochemotherapeutic activity and no DNA damage
49. Synthesis and antitumor activity of 2,5-bis(3′-indolyl)-furans and 3,5-bis(3′-indolyl)-isoxazoles, nortopsentin analogues
50. Thiopyrano[2,3- e]indol-2-ones: Angelicin heteroanalogues with potent photoantiproliferative activity
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