143 results on '"Manetti, D"'
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2. (E)-3-Furan-2-yl- N- p-tolyl-acrylamide and its Derivative DM489 Decrease Neuropathic Pain in Mice Predominantly by α7 Nicotinic Acetylcholine Receptor Potentiation
3. AMPA-receptor activation is involved in the antiamnesic effect of DM 232 (unifiram) and DM 235 (sunifiram)
4. Influence of ring size on the cognition-enhancing activity of DM235 and MN19, two potent nootropic drugs
5. Galeno e la ekdosis di Ippocrate: una nota testuale
6. (18 Hippocrates 24T) PRyl 530
7. Highly chiral muscarinic ligands: The discovery of (2S,2 ' R,3 ' S,5 ' R)-1-methyl-2-(2-methyl-1,3-oxathiolan-5-yl)pyrrolidine 3-sulfoxide methyl iodide, a potent, functionally selective, M-2 partial agonist
8. Muscarinic subtype affinity and functional activity profile of 1-methyl-2-(2-methyl-1,3-dioxolan-4-yl)pyrrolidine and 1-methyl-2-(2-methyl-1,3-oxathiolan-5-yl)pyrrolidine derivatives
9. Structure-affinity relationships of a unique nicotinic ligand: N1-dimethyl-N4-phenylpiperazinium iodide (DMPP)
10. Structure-Activity Relationships in 2,2-Diphenyl-2-ethylthioacetic Acid Esters: Unexpected Agonist Activity in a Series of Muscarinic Antagonists
11. Aspetti della terapia nel Corpus Hippocraticum
12. Reduced flexibility hybrids of the nicotinic agonists 1,1 dimethyl-4-acetylpiperazinium iodide and 2-(dimethylamino)methyl-5-methyl-cyclopentanone methiodide
13. Pharmacological Characterization of DM232 (Unifiram) and DM235 (Sunifiram), New Potent Cognition Enhancers
14. Enantioselective Synthesis and Preliminary Pharmacological Evaluation of the Enantiomers of Unifiram (DM232), a Potent Cognition-Enhancing Agent
15. AMPA-receptor activation is involved in the antiamnesic effect of DM�232 (unifiram) and DM�235 (sunifiram)
16. Differential analgesic activity of the enantiomers of atropine derivatives does not correlate with their muscarinic subtype selectivity
17. Un nuovo vocabolario greco-italiano
18. ChemInform Abstract: Reduced Flexibility Analogues of Analgesic and Cognition Enhancing . alpha.‐Tropanyl Esters.
19. Exploratory Chemistry toward the Identification of a New Class of Multidrug Resistance Reverters Inspired by Pervilleine and Verapamil Models
20. Design, Synthesis, and Preliminary Pharmacological Evaluation of a Set of Small Molecules That Directly Activate Gi Proteins
21. Structure-activity relationships in 2,2-diphenyl-2-ethylthioacetic acid esters
22. Structure−Affinity Relationships of a Unique Nicotinic Ligand: N<SUP>1</SUP>-Dimethyl-N<SUP>4</SUP>-phenylpiperazinium Iodide (DMPP)
23. Molecular Simplification of 1,4-Diazabicyclo[4.3.0]nonan-9-ones Gives Piperazine Derivatives That Maintain High Nootropic Activity
24. Design, Synthesis, and Preliminary Pharmacological Evaluation of 1,4-Diazabicyclo[4.3.0]nonan-9-ones as a New Class of Highly Potent Nootropic Agents
25. Design, Synthesis, and in Vitro Activity of Catamphiphilic Reverters of Multidrug Resistance: Discovery of a Selective, Highly Efficacious Chemosensitizer with Potency in the Nanomolar Range
26. Reduced-flexibility hybrids of the nicotinic agonists 1,1-dimethyl-4-acetylpiperazinium iodide and 2-(dimethylamino)methyl-5-methyl-cyclopentanone methiodide
27. Erratum: Antinociceptive profile of 3-α-tropanyl-(2-Cl)-acid phenoxybutyrate (SM-21): A novel analgesic with a presynaptic cholingeric mechanism of action (Journal of Pharmacology and Experimental Therapeutics (1997) 282:1 (430-439))
28. e me l’ovrare appaga
29. Ancient Medicine in the Galenic Corpus: The Story of a Concealment
30. Corrispondenza tra Achille Vogliano e Sergio Donadoni conservata nel Fondo Vogliano di Napoli
31. Ein Vertragsfragment aus dem Kloster des Apa Apollos in Bawit aus der Trierer Papyrussammlung
32. 18-21. Alcuni materiali greci e figurati da Soknopaiou Nesos
33. PHerc. 986 cr 8, pz 1: un aneddoto su Alessandro?
34. Bagni e digiuni in un papiro fiorentino: a proposito di P. Flor. III, 384 recto
35. 10. Ptolemäische Anthologie
36. Design of novel nicotinic ligands through 3D database searching
37. La Confederazione generale dell'industria italiana e la definizione della piccola- media industria nel secondo dopoguerra (anni 1940- 70)
38. Tommaso Fanfani e il dibattito storiografico sulle corporazioni nell'Italia dell'età moderna
39. La banca in Italia dall’Unità ad oggi: azienda, agenzia, impresa
40. The Decisions of Consciousness and the Consciousness of Decisions
41. Synthesis and biological evaluation of 3,7-diazabicyclo[4.3.0]nonan-8-ones as potential nootropic and analgesic drugs
42. Design, synthesis and preliminary evaluation of a series of histone deacetylase inhibitors carrying a benzodiazepine ring
43. Novel psychoplastogen DM506 reduces cue-induced heroin-seeking and inhibits tonic GABA currents in the Prelimbic Cortex.
44. Non-hallucinogenic compounds derived from iboga alkaloids alleviate neuropathic and visceral pain in mice through a mechanism involving 5-HT 2A receptor activation.
45. Dual Inhibitors of P-gp and Carbonic Anhydrase XII (hCA XII) against Tumor Multidrug Resistance with Piperazine Scaffold.
46. The novel non-hallucinogenic compound DM506 (3-methyl-1,2,3,4,5,6-hexahydroazepino[4,5-b]indole) induces sedative- and anxiolytic-like activity in mice by a mechanism involving 5-HT 2A receptor activation.
47. Synthetic Approaches to Piperazine-Containing Drugs Approved by FDA in the Period of 2011-2023.
48. Tetrazole and oxadiazole derivatives as bioisosteres of tariquidar and elacridar: New potent P-gp modulators acting as MDR reversers.
49. The Antinociceptive Activity of (E)-3-(thiophen-2-yl)- N -(p-tolyl)acrylamide in Mice Is Reduced by (E)-3-(furan-2-yl)- N -methyl- N -(p-tolyl)acrylamide Through Opposing Modulatory Mechanisms at the α7 Nicotinic Acetylcholine Receptor.
50. Chemical, Pharmacological, and Structural Characterization of Novel Acrylamide-Derived Modulators of the GABA A Receptor.
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