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Simona Bindi
Observed names:
S. BINDI,
S. Bindi
Institution:
Nerviano Medical Sciences
Observed institutions:
University of the Basque Country,
Menarini Group (Italy),
Nerviano Medical Sciences,
University of Florence
OpenAlex ID:
A5026998411
1,4,5,6-Tetrahydropyrrolo[3,4-c]pyrazoles: Identification of a Potent Aurora Kinase Inhibitor with a Favorable Antitumor Kinase Inhibition Profile
2006
·
Daniele Fancelli
, Jürgen Moll
, et al.
·
Journal of Medicinal Chemistry
·
188
Potent and Selective Aurora Inhibitors Identified by the Expansion of a Novel Scaffold for Protein Kinase Inhibition
2005
·
Daniele Fancelli
, Daniela Berta
, et al.
·
Journal of Medicinal Chemistry
·
146
Optimization of pyrazole inhibitors of Coactivator Associated Arginine Methyltransferase 1 (CARM1)
2009
·
Tram Huynh
, Zhong Chen
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
86
Discovery of NMS-E973 as novel, selective and potent inhibitor of heat shock protein 90 (Hsp90)
2013
·
Maria Gabriella Brasca
, Sergio Mantegani
, et al.
·
Bioorganic & Medicinal Chemistry
·
35
A Concise β-Lactam Route to Short Peptide Segments Containing β,β-Disubstituted β-Amino Acids
1998
·
Claudio Palomo
, Mikel Oiarbide
, et al.
·
The Journal of Organic Chemistry
·
35
A Selective and General Access to Trisubstituted Oxetanes
1996
·
Alessandro Mordini
, Simona Bindi
, et al.
·
The Journal of Organic Chemistry
·
34
Thieno[3,2-c]pyrazoles: A novel class of Aurora inhibitors with favorable antitumor activity
2010
·
Simona Bindi
, Daniele Fancelli
, et al.
·
Bioorganic & Medicinal Chemistry
·
30
Stereoselective Access to Hydroxy Oxetanes and Tetrahydrooxepines through Isomerization of Oxiranyl Ethers
2001
·
Alessandro Mordini
, Simona Bindi
, et al.
·
The Journal of Organic Chemistry
·
30
Different Pathways in the Base-Promoted Isomerization of Benzyl Oxiranyl Ethers
1996
·
Alessandro Mordini
, Simona Bindi
, et al.
·
The Journal of Organic Chemistry
·
29
A Selective Access to Amino Hydroxy Oxetanes
1997
·
Alessandro Mordini
, Michela Valacchi
, et al.
·
The Journal of Organic Chemistry
·
24
Novel pyrrole carboxamide inhibitors of JAK2 as potential treatment of myeloproliferative disorders
2015
·
Maria Gabriella Brasca
, Paola Gnocchi
, et al.
·
Bioorganic & Medicinal Chemistry
·
21
Pyrrole-3-carboxamides as potent and selective JAK2 inhibitors
2014
·
Maria Gabriella Brasca
, Marcella Nesi
, et al.
·
Bioorganic & Medicinal Chemistry
·
20
2,6-Diketopiperazines from Amino Acids, from Solution-Phase to Solid-Phase Organic Synthesis
2001
·
Enzo Perrotta
, Maria Altamura
, et al.
·
Journal of Combinatorial Chemistry
·
15
Discovery and optimization of 4-pyrazolyl-2-aminopyrimidine derivatives as potent spleen tyrosine kinase (SYK) inhibitors
2024
·
Giovanni Cervi
, Roberto D'Alessio
, et al.
·
European Journal of Medicinal Chemistry
·
3
Preparation of heterobicyclic pyrazole derivatives as kinase inhibitors
2004
·
R. Tonani
, Simona Bindi
, et al.
·
3
ChemInform Abstract: A Concise β‐Lactam Route to Short Peptide Segments Containing β,β‐Disubstituted β‐Amino Acids.
1998
·
C. PALOMO
, M. OIARBIDE
, et al.
·
ChemInform
·
2
Abstract 5163: Characterization of NMS-E194, a selective and potent PERK inhibitor with efficacy in the KMS-11 multiple myeloma
2017
·
Claudia Perrera
, Maurizio Pulici
, et al.
·
Cancer Research
·
1
Corrigendum to “Discovery of NMS-E973 as novel, selective and potent inhibitor of heat shock protein 90 (Hsp90)” [Bioorg. Med. Chem. 21 (2013) 7047–7063]
2013
·
Maria Gabriella Brasca
, Sergio Mantegani
, et al.
·
Bioorganic & Medicinal Chemistry
·
1
Abstract A179: NMS-P113, a novel orally available JAK2 selective inhibitor
2015
·
Paola Gnocchi
, Maria Gabriella Brasca
, et al.
·
Molecular Cancer Therapeutics
structure of HSP90 with an inhibitor bound
2013
·
E. Casale
, M.G. Brasca
, et al.
·
Worldwide Protein Data Bank
Structure of Aurora-2 in complex with PHA-680626
2006
·
A.D. Cameron
, G. Izzo
, et al.
·
Worldwide Protein Data Bank
Structure of Aurora-2 in complex with PHA-739358
2006
·
A.D. Cameron
, G. Izzo
, et al.
·
Worldwide Protein Data Bank
Aurora-2 T287D T288D complexed with PHA-680632
2005
·
A.D. Cameron
, G. Izzo
, et al.
·
Worldwide Protein Data Bank
Design and Combinatorial Chemistry of Novel and Potent Aurora Kinase Inhibitors
2004
·
Daniele Fancelli
, Daniela Berta
, et al.
ChemInform Abstract: 2,6‐Diketopiperazines from Amino Acids: From Solution‐Phase to Solid‐Phase Organic Synthesis.
2002
·
Enzo Perrotta
, Maria Altamura
, et al.
·
ChemInform
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Works count:
33
Citation count:
703
H-index:
13
I10-index:
13
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