266 results on '"Mosti, Luisa"'
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2. Rational design, synthesis and biological evaluation of new 1,5-diarylpyrazole derivatives as CB 1 receptor antagonists, structurally related to rimonabant
3. Synthesis, biological evaluation and docking studies of 4-amino substituted 1 H-pyrazolo[3,4- d]pyrimidines
4. CoMFA and CoMSIA analyses on 1,2,3,4-tetrahydropyrrolo[3,4-b]indole and benzimidazole derivatives as selective CB2 receptor agonists
5. CoMFA and CoMSIA analyses on 4-oxo-1,4-dihydroquinoline and 4-oxo-1,4-dihydro-1,5-, -1,6- and -1,8-naphthyridine derivatives as selective CB2 receptor agonists
6. Acylthiocarbamates as non-nucleoside HIV-1 reverse transcriptase inhibitors: docking studies and ligand-based CoMFA and CoMSIA analyses
7. Computational studies of the binding mode and 3D-QSAR analyses of symmetric formimidoester disulfides: a new class of non-nucleoside HIV-1 reverse transcriptase inhibitor
8. Quinolinedione nucleus as a novel scaffold for A1 and A2A adenosine receptor antagonists
9. Exploring the binding features of rimonabant analogues and acyclic CB1 antagonists: docking studies and QSAR analysis
10. In silico rationalization of the structural and physicochemical requirements for photobiological activity in angelicine derivatives and their heteroanalogues
11. Exploring the molecular basis of selectivity in A1 adenosine receptors agonists: a case study
12. Affinity prediction on A 1 adenosine receptor agonists: The chemometric approach
13. Synthesis, biological evaluation and molecular modelling studies on benzothiadiazine derivatives as PDE4 selective inhibitors
14. Insights into structure–activity relationships from lipophilicity profiles of pyridin-2(1 H)-one analogs of the cardiotonic agent milrinone
15. Insights into structure–activity relationships from lipophilicity profiles of pyridin-2(1H)-one analogs of the cardiotonic agent milrinone
16. Synthesis, antimicrobial activity and molecular modeling studies of halogenated 4-[1 H-imidazol-1-yl(phenyl)methyl]-1,5-diphenyl-1 H-pyrazoles
17. Antiproliferative activity of new 1-aryl-4-amino-1 H-pyrazolo[3,4- d]pyrimidine derivatives toward the human epidermoid carcinoma A431 cell line
18. Synthesis of 1-(2-chloro-2-phenylethyl)-6-methylthio-1 H-pyrazolo[3,4- d]pyrimidines 4-amino substituted and their biological evaluation
19. Synthesis and pharmacological characterization of functionalized 2-pyridones structurally related to the cardiotonic agent milrinone
20. 4-Substituted 1,5-diarylpyrazole, analogues of celecoxib: synthesis and preliminary evaluation of biological properties
21. Synthesis of N-substituted- N-acylthioureas of 4-substituted piperazines endowed with local anaesthetic, antihyperlipidemic, antiproliferative activities and antiarrythmic, analgesic, antiaggregating actions
22. Toward the identification of the cardiac cGMP inhibited-phosphodiesterase catalytic site
23. Novel angular furo and thieno-quinolinones: synthesis and preliminary photobiological studies
24. Synthesis and biological evaluation of azole derivatives, analogues of bifonazole, with a phenylisoxazolyl or phenylpyrimidinyl moiety
25. 4-Dialkylamino-1-(5-substituted or unsubstituted 1-phenyl-1 H-pyrazol-4-yl)butan-1-ols: synthesis and evaluation of analgesic, anti-inflammatory and platelet anti-aggregating activities
26. 3-Acetyl-5-acylpyridin-2(1 H)-ones and 3-acetyl-7,8-dihydro-2,5(1 H,6 H)-quinolinediones: synthesis, cardiotonic activity and computational studies
27. Synthesis and biological evaluation of [α-(1,5-disubstituted 1 H-pyrazol-4-yl)benzyl]azoles, analogues of bifonazole
28. DNA–psoralens molecular recognition using molecular dynamics
29. Exploring the binding features of rimonabant analogues and acyclic CB1 antagonists: docking studies and 3D-QSAR analysis
30. New pyrazolo[3,4-b]pyridines antagonist of A1 adenosine receptors
31. Synthesis of indole imminun salts as key-intermediates in a convergent multi-step one-pot stereoselective synthesis of new potent antiproliferative Knoevenagel-type agent
32. Synthesis of new pyrazolo[3,4-b]pyridines: new selective A1 adenosine receptor antagonists
33. Synthesis of pyrazolo[3,4-d]pyridines selective antagonists of A1 adenosine receptors
34. 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
35. New halogenated 4-aminopyrazolo[3,4-b]pyridines A1 adenosine receptor ligands
36. A chemometric approach to predict A1 agonist effect of adenosine analogues
37. Modulazioni Strutturali in O-[2-(N-Ftalimmido)etil] Acil(Aril)Tiocarbammati, Inibitori Non-Nucleosidici della Transcrittasi Inversa di HIV-1
38. Ionization Behaviour and Tautomerism-Dependent Lipophilicity of Pyridine-2(1H)-one Cardiotonic Agents
39. Studio computazionale di complessi di intercalazione al buio DNA-psoraleni Pavia, 27-29 maggio 1999
40. Zups: the evolution of a new class of molecular descriptors
41. Riconoscimento molecolare DNA-psoraleni mediante tecniche di dinamica molecolare
42. Development of a new topographical model for myocardial cGI-PDE catalytic site
43. omega-Dialkylaminoalkil Ethers of Phenyl-(5-substituted 1-phenyl-1H-pyrazol-4-yl)methanols with Analgesic and Anti-inflammatory Activity
44. Molecular Modeling of DNA-psoralens complexes
45. Inotropic Agents. Synthesis and Structure-Activity Relationships of New Milrinone Related cAMP PDEIII inhibitors
46. Towards the identification of the cardiac cAMP phosphodiesterase receptor site
47. Synthesis and Preliminary Biological Evaluation of Novel N-Substituted 1-Amino-3-[1-methyl(phenyl)-1H-indazol-4-yloxy]-propan-2-ols Interesting as Potential Antiarrhythmic, Local Anaesthetic and Analgesic Agents
48. QSAR study on new cardiotonic agents related to milrinone
49. ChemInform Abstract: Synthesis of Angelicin Heteroanalogues: Preliminary Photobiological and Pharmacological Studies.
50. ChemInform Abstract: 3-Acetyl-5-acylpyridin-2(1H)-ones and 3-Acetyl-7,8-dihydro-2,5(1H,6H)-quinolinediones: Synthesis, Cardiotonic Activity, and Computational Studies.
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