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Risultati 11 - 20 di 22 (tempo di esecuzione: 0.025 secondi).

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Pyrazolo[3,4-d]pyrimidines as tyrosine kinase inhibitors: synthesis and biological evaluation

2018-01-01 Musumeci, F.; Greco, C.; Giacchello, I.; Crespan, E.; Maga, G.; Schenone, S.; Fallacara, A. L.; Molinari, A.; Botta, M.

Substituted pyrazolo[3,4-b]pyridines as potent A1 adenosine antagonists.

2017-01-01 Giacchello, I.; Musumeci, F.; Greco, C.; Sanna, M.; Schenone, S.; Trincavelli, M. L.; Tuccinardi, T.

SYNTHESIS AND BIOLOGICAL EVALUATION OF NEW 4-AMINO-PYRAZOLO[3,4-d]PYRIMIDINES AS POTENTIAL SRC KINASE INHIBITORS

2023-01-01 Falesiedi, M.; Cianciusi, A.; Carbone, A.; Musumeci, F.; Schenone, S.; Angelucci, A.; Sabetta, S.; Maga, G.; Crespan, E.

Synthesis of a new generation of potential anti-influenza agents targeting the PA-PB1 protein-protein interaction.

2021-01-01 Cianciusi, A.; Schenone, S.; Musumeci, F.; D’Agostino, I.

Synthesis of a new generation of pyrazolo[3,4-d]pyrimidine as SGK-1 inhibitors.

2017-01-01 Greco, C.; Sanna, M.; Musumeci, F.; Giacchello, I.; Perrotti, N.; Alcaro, S.; Ortuso, F.; Schenone, S.

Synthesis of a new generation of pyrazolo[3,4-d]pyrimidines as Fyn inhibitors

2017-01-01 Sanna, M.; Greco, C.; Musumeci, F.; Giacchello, I.; Schenone, S.; Fallacara, A. L.; Trist, I. M.; Botta, M.

Synthesis of a new series of optimized pyrazolo[3,4‑d]pyrimidines as Src Inhibitors

2021-01-01 Cianciusi, Annarita; Carbone, Anna; Musumeci, Francesca; Schenone, Silvia

Synthesis of a small library of potential SGK1 inihibitors

2018-01-01 Greco, C.; Musumeci, F.; Giacchello, I.; Perrotti, N.; Alcaro, S.; Ortuso, F.; Schenone, S.

Synthesis of heterocyclic compounds to be tested as potentiators or correctors of mutant CFTR in cystic fibrosis

2016-01-01 Musumeci, F.; Sanna, M.; Giacchello, I.; Mazzei, M.; Schenone, S.

Synthesis of hybrid small molecules as potential PA-PB1 heterodimer disruptors of Influenza virus Polymerase

2021-01-01 Cianciusi, A.; Musumeci, F.; Carbone, A.; D’Agostino, I.; Schenone, S.

Titolo	Data di pubblicazione	Autore(i)
Pyrazolo[3,4-d]pyrimidines as tyrosine kinase inhibitors: synthesis and biological evaluation	1-gen-2018	Musumeci, F.; Greco, C.; Giacchello, I.; Crespan, E.; Maga, G.; Schenone, S.; Fallacara, A. L.; Molinari, A.; Botta, M.
Substituted pyrazolo[3,4-b]pyridines as potent A1 adenosine antagonists.	1-gen-2017	Giacchello, I.; Musumeci, F.; Greco, C.; Sanna, M.; Schenone, S.; Trincavelli, M. L.; Tuccinardi, T.
SYNTHESIS AND BIOLOGICAL EVALUATION OF NEW 4-AMINO-PYRAZOLO[3,4-d]PYRIMIDINES AS POTENTIAL SRC KINASE INHIBITORS	1-gen-2023	Falesiedi, M.; Cianciusi, A.; Carbone, A.; Musumeci, F.; Schenone, S.; Angelucci, A.; Sabetta, S.; Maga, G.; Crespan, E.
Synthesis of a new generation of potential anti-influenza agents targeting the PA-PB1 protein-protein interaction.	1-gen-2021	Cianciusi, A.; Schenone, S.; Musumeci, F.; D’Agostino, I.
Synthesis of a new generation of pyrazolo[3,4-d]pyrimidine as SGK-1 inhibitors.	1-gen-2017	Greco, C.; Sanna, M.; Musumeci, F.; Giacchello, I.; Perrotti, N.; Alcaro, S.; Ortuso, F.; Schenone, S.
Synthesis of a new generation of pyrazolo[3,4-d]pyrimidines as Fyn inhibitors	1-gen-2017	Sanna, M.; Greco, C.; Musumeci, F.; Giacchello, I.; Schenone, S.; Fallacara, A. L.; Trist, I. M.; Botta, M.
Synthesis of a new series of optimized pyrazolo[3,4‑d]pyrimidines as Src Inhibitors	1-gen-2021	Cianciusi, Annarita; Carbone, Anna; Musumeci, Francesca; Schenone, Silvia
Synthesis of a small library of potential SGK1 inihibitors	1-gen-2018	Greco, C.; Musumeci, F.; Giacchello, I.; Perrotti, N.; Alcaro, S.; Ortuso, F.; Schenone, S.
Synthesis of heterocyclic compounds to be tested as potentiators or correctors of mutant CFTR in cystic fibrosis	1-gen-2016	Musumeci, F.; Sanna, M.; Giacchello, I.; Mazzei, M.; Schenone, S.
Synthesis of hybrid small molecules as potential PA-PB1 heterodimer disruptors of Influenza virus Polymerase	1-gen-2021	Cianciusi, A.; Musumeci, F.; Carbone, A.; D’Agostino, I.; Schenone, S.

Risultati 11 - 20 di 22 (tempo di esecuzione: 0.025 secondi).

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Pyrazolo[3,4-d]pyrimidines as tyrosine kinase inhibitors: synthesis and biological evaluation

Substituted pyrazolo[3,4-b]pyridines as potent A1 adenosine antagonists.

SYNTHESIS AND BIOLOGICAL EVALUATION OF NEW 4-AMINO-PYRAZOLO[3,4-d]PYRIMIDINES AS POTENTIAL SRC KINASE INHIBITORS

Synthesis of a new generation of potential anti-influenza agents targeting the PA-PB1 protein-protein interaction.

Synthesis of a new generation of pyrazolo[3,4-d]pyrimidine as SGK-1 inhibitors.

Synthesis of a new generation of pyrazolo[3,4-d]pyrimidines as Fyn inhibitors

Synthesis of a new series of optimized pyrazolo[3,4‑d]pyrimidines as Src Inhibitors

Synthesis of a small library of potential SGK1 inihibitors

Synthesis of heterocyclic compounds to be tested as potentiators or correctors of mutant CFTR in cystic fibrosis

Synthesis of hybrid small molecules as potential PA-PB1 heterodimer disruptors of Influenza virus Polymerase

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