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Massimiliano Fonsi
Observed names:
Fonsi, M.,
M. Fonsi
Observed institutions:
Merck & Co., Inc., Rahway, NJ, USA (United States),
Oregon Health & Science University,
Addex Therapeutics (Switzerland),
MSD (Italy),
Sapienza University of Rome
ORCID:
0000-0003-4549-1483
Observed ORCID:
0000-0003-4549-1483
OpenAlex ID:
A5076006178
Discovery of 2-{4-[(3S)-Piperidin-3-yl]phenyl}-2H-indazole-7-carboxamide (MK-4827): A Novel Oral Poly(ADP-ribose)polymerase (PARP) Inhibitor Efficacious in BRCA-1 and -2 Mutant Tumors
2009
·
Philip Jones
, Sergio Altamura
, et al.
·
Journal of Medicinal Chemistry
·
325
Characterization of the Novel Positive Allosteric Modulator of the Metabotropic Glutamate Receptor 4 ADX88178 in Rodent Models of Neuropsychiatric Disorders
2014
·
Mikhail Kalinichev
, Emmanuel Le Poul
, et al.
·
Journal of Pharmacology and Experimental Therapeutics
·
71
PDF
Design and Synthesis of Bicyclic Pyrimidinones as Potent and Orally Bioavailable HIV-1 Integrase Inhibitors
2008
·
Ester Muraglia
, Olaf Kinzel
, et al.
·
Journal of Medicinal Chemistry
·
53
Discovery of a Potent Class I Selective Ketone Histone Deacetylase Inhibitor with Antitumor Activity in Vivo and Optimized Pharmacokinetic Properties
2009
·
Olaf Kinzel
, Laura Llauger-Bufi
, et al.
·
Journal of Medicinal Chemistry
·
46
High-Throughput Microsomal Stability Assay for Screening New Chemical Entities in Drug Discovery
2008
·
Massimiliano Fonsi
, Maria V. Orsale
, et al.
·
SLAS DISCOVERY
·
43
PDF
Identification of MK-5710 ((8aS)-8a-methyl-1,3-dioxo-2-[(1S,2R)-2-phenylcyclo- propyl]-N-(1-phenyl-1H-pyrazol-5-yl)hexahydro-imidazo[1,5-a]pyrazine-7(1H)-carboxamide), a potent smoothened antagonist for use in Hedgehog pathway dependent malignancies, Part 2
2011
·
Olaf Kinzel
, Anna Alfieri
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
37
Intra-Articular Hyaluronic Acid and Chondroitin Sulfate: Pharmacokinetic Investigation in Osteoarthritic Rat Models
2019
·
Massimiliano Fonsi
, Abdel-Ilah El Amrani
, et al.
·
Current Therapeutic Research
·
36
PDF
N-(2-alkylaminoethyl)-4-(1,2,4-oxadiazol-5-yl)piperazine-1-carboxamides as highly potent smoothened antagonists
2011
·
Ester Muraglia
, Jesus M. Ontoria
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
25
Allometric Scaling Approaches for Predicting Human Pharmacokinetic of a Locked Nucleic Acid Oligonucleotide Targeting Cancer-Associated miR-221
2019
·
Maria Teresa Di Martino
, Mariamena Arbitrio
, et al.
·
Cancers
·
22
PDF
The metabolism and disposition of a potent inhibitor of hepatitis C virus NS3/4A protease
2010
·
E. Monteagudo
, M. Fonsi
, et al.
·
Xenobiotica
·
17
High-Throughput Radiometric CYP2C19 Inhibition Assay Using Tritiated (S)-Mephenytoin
2007
·
Annalise Di Marco
, Antonella Cellucci
, et al.
·
Drug Metabolism and Disposition
·
15
Optimization of a series of potent and selective ketone histone deacetylase inhibitors
2008
·
Giovanna Pescatore
, Olaf Kinzel
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
12
Direct comparison of UDP-glucuronosyltransferase and cytochrome P450 activities in human liver microsomes, plated and suspended primary human hepatocytes from five liver donors
2017
·
Shalenie P. den Braver-Sewradj
, Michiel W. den Braver
, et al.
·
European Journal of Pharmaceutical Sciences
·
10
PDF
Metabolism-related liabilities of a potent histone deacetylase (HDAC) inhibitor and relevance of the route of administration on its metabolic fate
2009
·
M. Fonsi
, F. Fiore
, et al.
·
Xenobiotica
·
7
Scaling approaches for the prediction of human clearance of LNA-i-mir-221: A retrospective validation
2024
·
Massimiliano Fonsi
, Jacques Fulbert
, et al.
·
Current Research in Pharmacology and Drug Discovery
·
4
Methoxy-ether and crown-ether derivatives of tetrahomodioxa- and octahomotetraoxacalix[4]arenes
2001
·
Bernardo Masci
, Stefano Saccheo
, et al.
·
Acta Crystallographica Section C Crystal Structure Communications
·
4
Extrahepatic Metabolism may Complicate the IVIVC in Rats
2014
·
Massimiliano Fonsi
·
Drug Metabolism Letters
·
2
Assessment of Allometric Scaling Methods for the Prediction of Human Pharmacokinetic of LNA ‐i‐ miR ‐221
2026
·
Hadija Marchiori
, Michele Schiavon
, et al.
·
CPT Pharmacometrics & Systems Pharmacology
PDF
Translational Pharmacokinetic-Pharmacodynamic Modeling Framework for Protein Degraders in Oncology Drug Discovery
2026
·
Massimiliano Fonsi
, Radha Ramakrishnan
, et al.
·
Research Square
PDF
Hepatic and thyroid effects of phenobarbital in the minipig
2018
·
J. Boje Nielsen
, J. Decorde
, et al.
·
Toxicology Letters
Thyroid hormone perturbation in a minipig model
2018
·
Pramila Singh
, Jonas Boje Nielsen
, et al.
·
Reproductive Toxicology
Basal hepatic CYP activities in albino (Sprague–Dawley) and pigmented (Long Evans) rats
2017
·
Walid Touati
, Pramila Singh
, et al.
·
Toxicology Letters
Determination of thyroxine (T4) in mouse plasma by microsampling
2016
·
P. Singh
, J. Perron
, et al.
·
Toxicology Letters
ChemInform Abstract: Methoxy‐ether and Crown‐ether Derivatives of Tetrahomodioxa‐ and Octahomotetraoxacalix[4]arenes
2001
·
Bernardo Masci
, Stefano Saccheo
, et al.
·
ChemInform
CCDC 170206: Experimental Crystal Structure Determination
2001
·
Masci, B.
, Saccheo, S.
, et al.
·
The Cambridge Structural Database
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Works count:
28
Citation count:
729
H-index:
12
I10-index:
13
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