G. Diamantini

发表

Design and synthesis of melatonin receptors agonists and antagonists.

M. Mor, G. Tarzia, G. Spadoni, 2000, Farmaco.

Assessment of antioxidant capacity of energy drinks, energy gels and sport drinks in comparison with coffee and tea

D. Angelino, P. Ninfali, G. Diamantini, 2015 .

Melatonin receptor ligands: synthesis of new melatonin derivatives and comprehensive comparative molecular field analysis (CoMFA) study.

R. Nonno, M. Mor, G. Tarzia, 1998, Journal of medicinal chemistry.

Antioxidant and cytoprotective activity of indole derivatives related to melatonin.

Claudia Silva, Marco Mor, Federica Vacondio, 2003, Advances in experimental medicine and biology.

1-(2-Alkanamidoethyl)-6-methoxyindole derivatives: a new class of potent indole melatonin analogues.

R. Nonno, G. Tarzia, F. Fraschini, 1997, Journal of medicinal chemistry.

2-[N-Acylamino(C1-C3)alkyl]indoles as MT1 melatonin receptor partial agonists, antagonists, and putative inverse agonists.

R. Nonno, A. Tontini, M. Mor, 1998, Journal of medicinal chemistry.

2-N-acylaminoalkylindoles: design and quantitative structure-activity relationship studies leading to MT2-selective melatonin antagonists.

R. Nonno, A. Tontini, M. Mor, 2001, Journal of medicinal chemistry.

Further Highlighting on the Prevention of Oxidative Damage by Polyphenol-Rich Wine Extracts.

E. Falcieri, S. Salucci, G. Diamantini, 2017, Journal of medicinal food.

Plant-derived phenolic compounds prevent the DNA single-strand breakage and cytotoxicity induced by tert-butylhydroperoxide via an iron-chelating mechanism.

G. Tarzia, P. Sestili, O. Cantoni, 2002, The Biochemical journal.

Synthesis and Biological Evaluation of a γ-Cyclodextrin-based Formulation of the Anticancer Agent 5,6,11,12,17,18,23,24-Octahydrocyclododeca[1,2-b:4,5-b’:7,8-b’’:10,11-b’’’]tetraindole (CTet)

A. Duranti, A. Tontini, M. Magnani, 2010, Molecules.

Profibrinolytic activities of chemically modified heparins with very low anticoagulant activities.

M. Mantovani, G. Diamantini, R. Pescador, 1989, Thrombosis research.

Betacyanins enhance vitexin-2-O-xyloside mediated inhibition of proliferation of T24 bladder cancer cells.

M. Emanuelli, P. Ninfali, T. Armeni, 2016, Food & function.

Melatonin antagonizes apoptosis via receptor interaction in U937 monocytic cells

L. Ghibelli, G. Tarzia, F. Radogna, 2007, Journal of pineal research.

The anticoagulant, hepatic lipase-releasing and lipoprotein lipase-releasing activities of several natural and chemically modified heparins differ.

M. Mantovani, G. Diamantini, R. Pescador, 1987, Biochemical pharmacology.

Retention of antilipemic activity by periodate-oxidized non-anticoagulant heparins.

G. Torri, B. Casu, M. Mantovani, 1986, Arzneimittel-Forschung.

Nutritional characterization of naked and dehulled oat cultivar samples at harvest and after storage

P. Ninfali, R. Redaelli, G. Diamantini, 2016 .

Antimicrobial activity of two propolis samples against human Campylobacter jejuni.

V. Patrone, R. Campana, W. Baffone, 2009, Journal of medicinal food.

Synthesis, pharmacological characterization and QSAR studies on 2-substituted indole melatonin receptor ligands.

R. Nonno, M. Mor, G. Tarzia, 2001, Bioorganic & medicinal chemistry.

1-(2-Alkanamidoethyl)-6-methoxyindole derivatives: a new class of potent indole melatonin analogues.

R. Nonno, G. Tarzia, F. Fraschini, 1997, Journal of medicinal chemistry.

A Convenient and Easy Synthesis of γ-Nitro-α-Acetamido Esters

R. Ballini, G. Diamantini, C. Balsamini, 2005 .

Conformationally restrained melatonin analogues: synthesis, binding affinity for the melatonin receptor, evaluation of the biological activity, and molecular modeling study.

R. Nonno, M. Mor, G. Tarzia, 1997, Journal of medicinal chemistry.

Synthesis, antioxidant activity and structure–activity relationships for a new series of 2‐(N‐acylaminoethyl)indoles with melatonin‐like cytoprotective activity

Claudia Silva, Marco Mor, Federica Vacondio, 2006, Journal of pineal research.

A NEW SYNTHESIS OF 2-SUBSTITUTED DL-TRYPTOPHAN DERIVATIVES

A. Duranti, A. Tontini, G. Spadoni, 1995 .

Honey Flavonoids, Natural Antifungal Agents Against Candida Albicans

Manuela Blasa, E. Piatti, A. Accorsi, 2011 .

Indole Melatonin Agonists and Antagonists Derived by Shifting the Melatonin Side Chain from the C-3 to the N-1 or to the C-2 Indole Position

G. Tarzia, G. Spadoni, G. Diamantini, 1999, Neurosignals.

Synthesis, Enantiomeric Resolution, and Structure–Activity Relationship Study of a Series of 10,11‐Dihydro‐5H‐Dibenzo[a,d]cycloheptene MT2 Receptor Antagonists

M. Mor, G. Tarzia, F. Fraschini, 2007, ChemMedChem.

Metastable ion studies in the characterization of melatonin isomers

G. Tarzia, P. Traldi, G. Spadoni, 1998 .

Synthesis of (E)-8-(3-chlorostyryl)caffeine analogues leading to 9-deazaxanthine derivatives as dual A(2A) antagonists/MAO-B inhibitors.

Walter Cabri, Daniele Pala, Giovanni Piersanti, 2013, Journal of medicinal chemistry.

Electron impact ionization and fast atom bombardment mass spectrometry of some 3,3‐dimethyl‐1‐(isoxazol‐3‐yl)triazenes, a new class of potential anticancer agents

A. Tontini, G. Tarzia, P. Traldi, 1995 .

(E)-3-(2-(N-phenylcarbamoyl)vinyl)pyrrole-2-carboxylic acid derivatives. A novel class of glycine site antagonists.

G. Tedesco, A. Reggiani, A. Tontini, 1998, Journal of Medicinal Chemistry.

3-(2-Carbamoylvinyl)-4,5-dimethylpyrrole-2-carboxylic acids as ligands at the NMDA glycine-binding site: a study on the 2-carbamoylvinyl chain modification.

A. Tontini, G. Tarzia, G. Spadoni, 1999, Farmaco.

The effect of mechanical processing on avenanthramide and phenol levels in two organically grown Italian oat cultivars

P. Ninfali, G. Diamantini, E. Antonini, 2017, Journal of Food Science and Technology.

Flavonoids from italian multifloral honeys reduce the extracellular ferricyanide in human red blood cells.

Manuela Blasa, E. Piatti, A. Accorsi, 2006, Journal of agricultural and food chemistry.

Indole‐based analogs of melatonin: in vitro antioxidant and cytoprotective activities

M. Mor, G. Tarzia, M. Zusso, 2004, Journal of pineal research.

CORRELATION OF THE ANTIMETASTATIC PROPERTIES OF ARYLTRIAZENES WITH THEIR ELECTRON IMPACT IONIZATION MASS SPECTROMETRY

A. Tontini, G. Tarzia, P. Traldi, 1997 .

Letter to the Editor: Correlation of the mutagenic properties of aryl‐ and heteroaryltriazenes with their electron ionization induced fragmentation

A. Tontini, G. Tarzia, P. Traldi, 1996 .

Correlation of the mutagenic properties of aryl- and heteroaryltriazenes with their electron ionization induced fragmentation

A. Tontini, G. Tarzia, P. Traldi, 1996 .

Tricyclic alkylamides as melatonin receptor ligands with antagonist or inverse agonist activity.

M. Mor, G. Tarzia, F. Fraschini, 2004, Journal of Medicinal Chemistry.

Synthesis of 1-(isoxazol-3-yl)triazene derivatives. Antimetastatic activity of 3,3-dimethyl-1-(5-methylisoxazol-3-yl)triazene

A. Tontini, G. Tarzia, V. Rapozzi, 1996 .

Reassessing the melatonin pharmacophore--enantiomeric resolution, pharmacological activity, structure analysis, and molecular modeling of a constrained chiral melatonin analogue.

M. Mor, G. Tarzia, V. Lucini, 2006, Bioorganic & medicinal chemistry.

Antimicrobial activity of two propolis samples against human Campylobacter jejuni.

V. Patrone, R. Campana, W. Baffone, 2009, Journal of Medicinal Food.