283 results on '"Ranise, Angelo"'
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2. Further SAR studies on bicyclic basic merbarone analogues as potent antiproliferative agents
3. Homology modeling in tandem with 3D-QSAR analyses: A computational approach to depict the agonist binding site of the human CB2 receptor
4. Parallel synthesis, molecular modelling and further structure–activity relationship studies of new acylthiocarbamates as potent non-nucleoside HIV-1 reverse transcriptase inhibitors
5. Novel modifications in the series of O-(2-phthalimidoethyl)- N-substituted thiocarbamates and their ring-opened congeners as non-nucleoside HIV-1 reverse transcriptase inhibitors
6. N-Acylated and N, N′-diacylated imidazolidine-2-thione derivatives and N, N′-diacylated tetrahydropyrimidine-2(1 H)-thione analogues: Synthesis and antiproliferative activity
7. 6-Amino-4-oxo-1,3-diphenyl-2-thioxo-1,2,3,4-tetrahydropyrimidine-5-carbonyl derivatives as a new class of potent inhibitors of Interleukin-8-induced neutrophil chemotaxis
8. Rational design, synthesis and biological evaluation of new 1,5-diarylpyrazole derivatives as CB 1 receptor antagonists, structurally related to rimonabant
9. Parallel one-pot synthesis and structure–activity relationship study of symmetric formimidoester disulfides as a novel class of potent non-nucleoside HIV-1 reverse transcriptase inhibitors
10. Thiocarbamates as non-nucleoside HIV-1 reverse transcriptase inhibitors. Part 1: Parallel synthesis, molecular modelling and structure–activity relationship studies on O-[2-(hetero)arylethyl]- N-phenylthiocarbamates
11. Thiocarbamates as non-nucleoside HIV-1 reverse transcriptase inhibitors. Part 2: Parallel synthesis, molecular modelling and structure–activity relationship studies on analogues of O-(2-phenylethyl)- N-phenylthiocarbamate
12. (Hetero)aroyl esters of 2-(N-phthalimido)ethanol and analogues: parallel synthesis, anti-HIV-1 activity and cytotoxicity
13. Exploring the molecular basis of selectivity in A1 adenosine receptors agonists: a case study
14. New 1,3,4-thiadiazole derivatives endowed with analgesic and anti-inflammatory activities
15. Affinity prediction on A 1 adenosine receptor agonists: The chemometric approach
16. Synthesis, antiplatelet and antithrombotic activities of new 2-substituted benzopyrano[4,3-d]pyrimidin-4-cycloamines and 4-amino/cycloamino-benzopyrano[4,3-d]pyrimidin-5-ones
17. A Successful Application Of Parallel Synthesis To Computer-assisted Structural Optimization Of New Leads Targeting Human Immunodeficiency Virus-1 Reverse Transcriptase The Case Of Acylthiocarbamates And Thiocarbamates
18. Antiproliferative activity of new 1-aryl-4-amino-1 H-pyrazolo[3,4- d]pyrimidine derivatives toward the human epidermoid carcinoma A431 cell line
19. Synthesis of 1-(2-chloro-2-phenylethyl)-6-methylthio-1 H-pyrazolo[3,4- d]pyrimidines 4-amino substituted and their biological evaluation
20. Synthesis, antimicrobial activity and molecular modeling studies of halogenated 4-[1 H-imidazol-1-yl(phenyl)methyl]-1,5-diphenyl-1 H-pyrazoles
21. Synthesis and pharmacological evaluation of 5 H-[1]benzopyrano[4,3-d]pyrimidines effective as antiplatelet/analgesic agents
22. Synthesis and antiproliferative activity of basic thioanalogues of merbarone
23. Capitolo 14 - Anticonvulsivanti
24. Capitolo 19 - Agenti cardiovascolari
25. Capitolo 18 - Farmaci attivi sul sistema renale
26. Unprecedented one-pot synthesis of pharmaceutical interest derivatives via in situ condensation of heterocyclic iminium salts with nitrogen nucleophiles
27. Parallel synthesis of O-phenoxyethyl and O-adamantyl N-acyl thiocarbamates endowed with antiproliferative activity
28. Reattivita' di accettori di Michael atipici con nucleofili azotati
29. Crystal structures of HIV-1 reverse transcriptase in complexes with thiocarbamate non-nucleoside inhibitors
30. Further SAR studies on bicyclic basic merbarone analogues as potent antiproliferative agents
31. Non-receptor tyrosine kinase Fes as a target in oncology
32. 5-Substituted derivatives of 6-amino-1,3-diphenyl-2-thioxo-2,3-dihydropyrimidin-4(1H)-one as a new class of potent inhibitors of interleukin 8-induced neutrophil chemotaxis
33. Synthesis of indole imminun salts as key-intermediates in a convergent multi-step one-pot stereoselective synthesis of new potent antiproliferative Knoevenagel-type agent
34. Synthesis of new pyrazolo [3,4-d]pyrimidines Bcr-Abl tyrosine kinase inhibitors
35. Virtual screening and structure based drug design of new Fes/Fps kinase domain inhibitors
36. Synthesis of new pyrazolo[3,4-b]pyridines: new selective A1 adenosine receptor antagonists
37. 2,3-Dihydro-1H-imidazo[1,2-b]pyrazole derivatives as potential neutrophils functions inhibitors
38. X-ray analysis of HIV-1 reverse transcriptase in complex with thiocarbamates: structure-based design and synthesis of new analogues
39. New pyrazolo[3,4-d]pyrimidines 4-benzylamino substituted endowed with antiproliferative activity on chronic myeloid leukemia cell line
40. One-pot Stereoselective Synthesis of Knoevenageltype Derivatives Via Condensation of N-Methyleniminium Salts of Ethylenethiourea and Ethyleneurea with Active Methylene Reagents
41. Synthesis of pyrazolo[3,4-d]pyridines selective antagonists of A1 adenosine receptors
42. Structure-based Design, Parallel Synthesis, SAR and Molecular Modelling Studies of Thiocarbamates, New Potent Non-Nucleoside HIV-1 Reverse Transcriptase Inhibitor Isosteres of Phenethylthiazolylthiourea (PETT) Derivatives
43. New halogenated 4-aminopyrazolo[3,4-b]pyridines A1 adenosine receptor ligands
44. 5-alkoxy-2-hydrazino and 5-methoxy-2-amino-5H-[1]benzopyrano[4,3-d]pyrimidines: synthesis and pharmacological activity
45. New N-substituted N'[1-(2-hydroxy-2-phenylethyl)-1H-pyrazol-5-yl]ureas inhibiting CXCL8 induced neutrophil chemotaxis
46. A chemometric approach to predict A1 agonist effect of adenosine analogues
47. Benzopirano[4,3-d]pirimidine e Benzopirano[4,3-d]pirimidin-5-oni 2,4-disostituiti: sintesi ed attività antipiastrinica
48. Studi Cristallografici di Complessi tra Transcrittasi Inversa di HIV-1 e Derivati Tiocarbammici a Scheletro Ftalimmidico, Inibitori Non Nucleosidici Correlati ai Derivati PETT
49. Sintesi Convergente 'One-Pot' di Aciltiocarbammati ad Attività Antiproliferativa
50. Sintesi di Esteri Tienopirimidinici ad Attività Antiproliferativa
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