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/vufind/Search/Results?lookfor=%22Bagnolini%2C+Greta%22&type=Person&sort=year
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PubPharm (11)
1
An 19F NMR fragment-based approach for the discovery and development of BRCA2-RAD51 inhibitors to pursuit synthetic lethality in combination with PARP inhibition in pancreatic cancer
enthalten in:
European journal of medicinal chemistry
| 2024
von
Myers, S.
|
Poppi, L.
|
Rinaldi, F.
| +13
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2
Recognizing the power of machine learning and other computational methods to accelerate progress in small molecule targeting of RNA
enthalten in:
RNA (New York, N.Y.)
| 2023
von
Bagnolini, G.
|
Luu, T.
|
Hargrove, A.
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3
COMPOUNDS AND COMPOSITIONS FOR THE TREATMENT OF TUMORS
enthalten in:
Europäisches Patentamt
| 2022
von
CAVALLI ANDREA
|
MILANO DOMENICO
|
MANERBA MARCELLA
| +9
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4
Identification of RAD51-BRCA2 Inhibitors Using N-Acylhydrazone-Based Dynamic Combinatorial Chemistry
enthalten in:
ACS medicinal chemistry letters
| 2022
von
Bagnolini, G.
|
Balboni, B.
|
Schipani, F.
| +10
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5
COMPOUNDS AND COMPOSITIONS FOR THE TREATMENT OF TUMORS
enthalten in:
Europäisches Patentamt
| 2021
von
CAVALLI ANDREA
|
MILANO DOMENICO
|
MANERBA MARCELLA
| +9
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6
Inhibition of Urease, a Ni-Enzyme : The Reactivity of a Key Thiol With Mono- and Di-Substituted Catechols Elucidated by Kinetic, Structural, and Theoretical Studies
enthalten in:
Angewandte Chemie (International ed. in English)
| 2021
von
Mazzei, L.
|
Contaldo, U.
|
Musiani, F.
| +4
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7
Design and synthesis of RAD51-BRCA2 disruptors that trigger synthetic lethality in pancreatic cancer in combination with Olaparib
Erschienen:
Dissertation, Alma Mater Studiorum - Università di Bologna, 2021
von
Bagnolini, G.
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8
Inhibition of Urease, a Ni‐Enzyme : The Reactivity of a Key Thiol With Mono‐ and Di‐Substituted Catechols Elucidated by Kinetic, Structural, and Theoretical Studies
enthalten in:
Angewandte Chemie
| 2021
von
Mazzei, L.
|
Contaldo, U.
|
Musiani, F.
| +4
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9
Inhibition of Urease, a Ni‐Enzyme : The Reactivity of a Key Thiol With Mono‐ and Di‐Substituted Catechols Elucidated by Kinetic, Structural, and Theoretical Studies
enthalten in:
Angewandte Chemie International Edition
| 2021
von
Mazzei, L.
|
Contaldo, U.
|
Musiani, F.
| +4
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10
Synthetic Lethality in Pancreatic Cancer : Discovery of a New RAD51-BRCA2 Small Molecule Disruptor That Inhibits Homologous Recombination and Synergizes with Olaparib
enthalten in:
Journal of medicinal chemistry
| 2020
von
Bagnolini, G.
|
Milano, D.
|
Manerba, M.
| +16
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European journal of medicinal chemistry
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RNA (New York, N.Y.)
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Thema
6
Journal Article
3
Antineoplastic Agents
3
BRCA2 Protein
3
EC 2.7.7.-
3
Rad51 Recombinase
2
615
2
A61K: Preparations for medical, dental, or toil...
2
A61P: Specific therapeutic activity of chemical...
2
BRCA2 protein, human
2
C07D: Heterocyclic compounds (macromolecular co...
2
Phthalazines
2
Piperazines
2
Poly(ADP-ribose) Polymerase Inhibitors
2
Research Support, Non-U.S. Gov't
2
Synthetic lethality
2
WOH1JD9AR8
2
che
2
olaparib
1
63231-63-0
1
Anticancer drugs
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Erscheinungszeitraum
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2020-
1
2010-2019
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