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Giovanna Pescatore
Observed institutions:
Merck & Co., Inc., Rahway, NJ, USA (United States),
Istituto di Chimica Biomolecolare,
IRBM,
Sapienza University of Rome
OpenAlex ID:
A5039592921
Discovery of Raltegravir, a Potent, Selective Orally Bioavailable HIV-Integrase Inhibitor for the Treatment of HIV-AIDS Infection
2008
·
Vincenzo Summa
, Alessia Petrocchi
, et al.
·
Journal of Medicinal Chemistry
·
653
Tetrazole thioacetanilides: Potent non-nucleoside inhibitors of WT HIV reverse transcriptase and its K103N mutant
2006
·
Ester Muraglia
, Olaf D. Kinzel
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
90
Discovery and Synthesis of HIV Integrase Inhibitors: Development of Potent and Orally Bioavailable N-Methyl Pyrimidones
2007
·
Cristina Gardelli
, Emanuela Nizi
, et al.
·
Journal of Medicinal Chemistry
·
67
A Novel Series of Potent and Selective Ketone Histone Deacetylase Inhibitors with Antitumor Activity in Vivo
2008
·
Philip Jones
, Sergio Altamura
, et al.
·
Journal of Medicinal Chemistry
·
59
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
A study on the chelation control in the regioselective opening of 2,3-bifunctionalized epoxides
2001
·
Giuliana Righi
, Giovanna Pescatore
, et al.
·
Tetrahedron
·
29
New stereoselective synthesis of the peptidic aminopeptidase inhibitors bestatin, phebestin and probestin
2003
·
Giuliana Righi
, Claudia D'Achille
, et al.
·
Tetrahedron Letters
·
28
Identification and SAR of novel pyrrolo[1,2-a]pyrazin-1(2H)-one derivatives as inhibitors of poly(ADP-ribose) polymerase-1 (PARP-1)
2009
·
Giovanna Pescatore
, Danila Branca
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
21
A novel base-mediated intramolecular hydroamination to build fused heteroaryl pyrazinones
2008
·
Laura Llauger
, Costanza Bergami
, et al.
·
Tetrahedron Letters
·
14
Dihydroxy-pyrimidine and N-methylpyrimidone HIV-integrase inhibitors: Improving cell based activity by the quaternarization of a chiral center
2009
·
Emanuela Nizi
, Maria Vittoria Orsale
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
12
Optimization of a series of potent and selective ketone histone deacetylase inhibitors
2008
·
Giovanna Pescatore
, Olaf Kinzel
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
12
The synthesis of tetrahydropyridopyrimidones as a new scaffold for HIV-1 integrase inhibitors
2007
·
Olaf D. Kinzel
, Edith Monteagudo
, et al.
·
Tetrahedron Letters
·
11
ChemInform Abstract: A Study on the Chelation Control in the Regioselective Opening of 2,3‐Bifunctionalized Epoxides.
2001
·
Giuliana Righi
, Giovanna Pescatore
, et al.
·
ChemInform
·
1
ChemInform Abstract: Identification and SAR of Novel Pyrrolo[1,2‐a]pyrazin‐1(2H)‐one Derivatives as Inhibitors of Poly(ADP‐Ribose) Polymerase‐1 (PARP‐1).
2010
·
Giovanna Pescatore
, et al. et al.
·
ChemInform
ChemInform Abstract: A Novel Base‐Mediated Intramolecular Hydroamination to Build Fused Heteroaryl Pyrazinones.
2009
·
Laura Llauger
, Costanza Bergami
, et al.
·
ChemInform
New Stereoselective Synthesis of the Peptidic Aminopeptidase Inhibitors Bestatin, Phebestin and Probestin.
2003
·
Giuliana Righi
, Claudia D'Achille
, et al.
·
ChemInform
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Works count:
17
Citation count:
1,096
H-index:
12
I10-index:
13
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