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Gabriele Amari
Observed names:
Amari, G.,
Amari, Gabriele,
G. AMARI,
G. Amari
Institution:
Chiesi (Italy)
Observed institutions:
University of Parma,
University of Milan,
University of Pavia,
AREA Science Park,
Salvat (Spain),
National Research Council,
Chiesi (Italy),
Institute of Crystallography,
University of Turin,
Politecnico di Milano
show all 10
OpenAlex ID:
A5034163162
CHF6001 I: A Novel Highly Potent and Selective Phosphodiesterase 4 Inhibitor with Robust Anti-Inflammatory Activity and Suitable for Topical Pulmonary Administration
2015
·
Nadia Moretto
, Paola Caruso
, et al.
·
Journal of Pharmacology and Experimental Therapeutics
·
77
Novel Class of Benzoic Acid Ester Derivatives as Potent PDE4 Inhibitors for Inhaled Administration in the Treatment of Respiratory Diseases
2014
·
Elisabetta Armani
, Gabriele Amari
, et al.
·
Journal of Medicinal Chemistry
·
47
Structural Determinants of Torpedo c alifornica Acetylcholinesterase Inhibition by the Novel and Orally Active Carbamate Based Anti-Alzheimer Drug Ganstigmine (CHF-2819)
2006
·
Cecilia Bartolucci
, Mariacristina Siotto
, et al.
·
Journal of Medicinal Chemistry
·
47
Bronchodilator Activity of (3R)-3-[[[(3-fluorophenyl)[(3,4,5-trifluorophenyl)methyl]amino] carbonyl]oxy]-1-[2-oxo-2-(2-thienyl)ethyl]-1-azoniabicyclo[2.2.2]octane bromide (CHF5407), a Potent, Long-Acting, and Selective Muscarinic M3 Receptor Antagonist
2010
·
G. Villetti
, F. Pastore
, et al.
·
Journal of Pharmacology and Experimental Therapeutics
·
28
Discovery of Diaryl Imidazolidin-2-one Derivatives, a Novel Class of Muscarinic M3 Selective Antagonists (Part 1)
2007
·
Ilaria Peretto
, Roberto Forlani
, et al.
·
Journal of Medicinal Chemistry
·
26
Synthesis, pharmacological evaluation, and structure–activity relationships of benzopyran derivatives with potent SERM activity
2004
·
Gabriele Amari
, Elisabetta Armani
, et al.
·
Bioorganic & Medicinal Chemistry
·
24
Discovery and Optimization of Thiazolidinyl and Pyrrolidinyl Derivatives as Inhaled PDE4 Inhibitors for Respiratory Diseases
2017
·
Laura Carzaniga
, Gabriele Amari
, et al.
·
Journal of Medicinal Chemistry
·
22
Discovery of Diaryl Imidazolidin-2-one Derivatives, a Novel Class of Muscarinic M3 Selective Antagonists (Part 2)
2007
·
Ilaria Peretto
, Claudia Fossati
, et al.
·
Journal of Medicinal Chemistry
·
16
Discovery of M3 Antagonist-PDE4 Inhibitor Dual Pharmacology Molecules for the Treatment of Chronic Obstructive Pulmonary Disease
2021
·
Elisabetta Armani
, Andrea Rizzi
, et al.
·
Journal of Medicinal Chemistry
·
12
Novel Basic Isoflavones as Inhibitors of Bone Resorption
2001
·
Maurizio Delcanale
, Gabriele Amari
, et al.
·
Helvetica Chimica Acta
·
12
Effects of 3-Phenyl-4-[[4-[2-(1-piperidinyl)ethoxy]phenyl]methyl]- 2 H-1-benzopyran-7-ol (CHF 4056), a Novel Nonsteroidal Estrogen Agonist/Antagonist, on Reproductive and Nonreproductive Tissue
2002
·
Elisabetta Galbiati
, Paola Lorenza Caruso
, et al.
·
Journal of Pharmacology and Experimental Therapeutics
·
11
Discovery of a Potent, Selective, and Orally Bioavailable Tool Compound for Probing the Role of Lysophosphatidic Acid Type 2 Receptor Antagonists in Fibrotic Disorders
2023
·
Elisabetta Armani
, Andrea Rizzi
, et al.
·
Journal of Medicinal Chemistry
·
10
The Molecular Structure and Crystal Organization Of Rac -terfenadine/β-cyclodextrin/tartaric Acid Multicomponent Inclusion Complex
2002
·
Alessia Bacchi
, Giancarlo Pelizzi
, et al.
·
Supramolecular chemistry
·
10
Pharmacological Actions of a Novel, Potent, Tissue-Selective Benzopyran Estrogen
2002
·
Elisabetta Galbiati
, Paola Lorenza Caruso
, et al.
·
Journal of Pharmacology and Experimental Therapeutics
·
10
The Crystal Structure of the Inclusion Complex of the Sodium Salt of Piroxicam with β-cyclodextrin
1998
·
Angiola Chiesi-villa
, Corrado Rizzoli
, et al.
·
Supramolecular chemistry
·
9
Erythroid differentiation ability of butyric acid analogues: Identification of basal chemical structures of new inducers of foetal haemoglobin
2015
·
Nicoletta Bianchi
, Cristiano Chiarabelli
, et al.
·
European Journal of Pharmacology
·
8
New method for the resolution of the enantiomers of 5,6-Dihydroxy-2-Methyl-Aminotetralin by selective derivatization and HPLC analysis: Application to biological fluids
1996
·
Ivano Rondelli
, Roberto Corsaletti
, et al.
·
Chirality
·
8
Solution‐ and Solid‐state Structures of the (—)‐n‐Heptylcarbamate of Geneseroline and Its Hydrochloride Salt
1995
·
Enrico Redenti
, Maurizio Delcanale
, et al.
·
Journal of Pharmaceutical Sciences
·
7
Optimization of M3 Antagonist–PDE4 Inhibitor (MAPI) Dual Pharmacology Molecules for the Treatment of COPD
2023
·
Andrea Rizzi
, Gabriele Amari
, et al.
·
Journal of Medicinal Chemistry
·
6
Synthesis of glycose carbamides and evaluation of the induction of erythroid differentiation of human erythroleukemic K562 cells
2008
·
Martina Landi
, Giorgio Catelani
, et al.
·
European Journal of Medicinal Chemistry
·
6
Differentiation of diastereomeric aminotetralins by metastable ion spectra of 2‐oxazolidinone derivatives upon electron‐impact ionization
1992
·
Antonio Selva
, Enrico Redenti
, et al.
·
Organic Mass Spectrometry
·
6
Geneserine hydrochloride
1994
·
A. Bacchi
, G. Pelizzi
, et al.
·
Acta Crystallographica Section C Crystal Structure Communications
·
2
Selective method for plasma quantitation of the stereoisomers of a new aminotetralin by high-performance liquid chromatography with electrochemical detection
1993
·
Ivano Rondelli
, Fabrizia Mariotti
, et al.
·
Journal of Chromatography B Biomedical Sciences and Applications
·
2
The soluble tris(acetylacetonato)vanadium/dialkylaluminium chloride system for alkene polymerization. Enhancement of activity by the use of dimethylaluminium chloride
1987
·
Antonino Giarrusso
, Gabriele Amari
, et al.
·
Die Makromolekulare Chemie Rapid Communications
·
2
Corrigendum to “Synthesis, pharmacological evaluation, and structure–activity relationships of benzopyran derivatives with potent SERM activity” [Bioorg. Med. Chem. 12 (2004) 3763]
2004
·
Gabriele Amari
, Elisabetta Armani
, et al.
·
Bioorganic & Medicinal Chemistry
·
1
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Works count:
34
Citation count:
410
H-index:
11
I10-index:
14
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