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Delia Preti

Showing results (31-40 of 98) with videos related to

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Bioorganic & Medicinal Chemistry|September 3, 2003
New strategies for the synthesis of A3 adenosine receptor antagonistsPier Giovanni Baraldi, Andrea Bovero, Francesca Fruttarolo, et al.
International Journal of Molecular Sciences|October 14, 2020
Discovery of Novel Fetal Hemoglobin Inducers through Small Chemical Library ScreeningGiulia Breveglieri, Salvatore Pacifico, Cristina Zuccato, et al.
Journal of Enzyme Inhibition and Medicinal Chemistry|August 25, 2018
Design, synthesis, in vitro antiproliferative activity and apoptosis-inducing studies of 1-(3',4',5'-trimethoxyphenyl)-3-(2'-alkoxycarbonylindolyl)-2-propen-1-one derivatives obtained by a molecular hybridisation approachDelia Preti, Romeo Romagnoli, Riccardo Rondanin, et al.
EJNMMI Radiopharmacy and Chemistry|May 5, 2024
Bifunctional octadentate pseudopeptides as Zirconium-89 chelators for immuno-PET applicationsValentina Albanese, Chiara Roccatello, Salvatore Pacifico, et al.
Medicinal Chemistry (Shariqah (United Arab Emirates))|November 11, 2008
Synthesis and biological evaluation of 2-aroyl-4-phenyl-5-hydroxybenzofurans as a new class of antitubulin agentsRomeo Romagnoli, Pier Giovanni Baraldi, Taradas Sarkar, et al.
Bioorganic & Medicinal Chemistry Letters|March 10, 2007
Hybrid molecules containing benzo[4,5]imidazo[1,2-d][1,2,4]thiadiazole and alpha-bromoacryloyl moieties as potent apoptosis inducers on human myeloid leukaemia cellsRomeo Romagnoli, Pier Giovanni Baraldi, Maria Dora Carrion, et al.
Bioorganic & Medicinal Chemistry|February 14, 2012
7-Substituted-pyrrolo[3,2-d]pyrimidine-2,4-dione derivatives as antagonists of the transient receptor potential ankyrin 1 (TRPA1) channel: a promising approach for treating pain and inflammationPier Giovanni Baraldi, Romeo Romagnoli, Giulia Saponaro, et al.
Journal of Medicinal Chemistry|July 8, 2005
New pyrrolo[2,1-f]purine-2,4-dione and imidazo[2,1-f]purine-2,4-dione derivatives as potent and selective human A3 adenosine receptor antagonistsPier Giovanni Baraldi, Delia Preti, Mojgan Aghazadeh Tabrizi, et al.
Journal of Medicinal Chemistry|July 22, 2005
New 2-arylpyrazolo[4,3-c]quinoline derivatives as potent and selective human A3 adenosine receptor antagonistsPier Giovanni Baraldi, Mojgan Aghazadeh Tabrizi, Delia Preti, et al.
Bioconjugate Chemistry|August 29, 2019
Tetrabranched Hetero-Conjugated Peptides as Bifunctional Agonists of the NOP and Mu Opioid ReceptorsSalvatore Pacifico, Valentina Albanese, Davide Illuminati, et al.
Pageof 10

Showing results (31-40 of 98) with videos related to

Sort By:
Pageof 10
Bioorganic & Medicinal Chemistry|September 3, 2003
New strategies for the synthesis of A3 adenosine receptor antagonistsPier Giovanni Baraldi, Andrea Bovero, Francesca Fruttarolo, et al.
International Journal of Molecular Sciences|October 14, 2020
Discovery of Novel Fetal Hemoglobin Inducers through Small Chemical Library ScreeningGiulia Breveglieri, Salvatore Pacifico, Cristina Zuccato, et al.
Journal of Enzyme Inhibition and Medicinal Chemistry|August 25, 2018
Design, synthesis, in vitro antiproliferative activity and apoptosis-inducing studies of 1-(3',4',5'-trimethoxyphenyl)-3-(2'-alkoxycarbonylindolyl)-2-propen-1-one derivatives obtained by a molecular hybridisation approachDelia Preti, Romeo Romagnoli, Riccardo Rondanin, et al.
EJNMMI Radiopharmacy and Chemistry|May 5, 2024
Bifunctional octadentate pseudopeptides as Zirconium-89 chelators for immuno-PET applicationsValentina Albanese, Chiara Roccatello, Salvatore Pacifico, et al.
Medicinal Chemistry (Shariqah (United Arab Emirates))|November 11, 2008
Synthesis and biological evaluation of 2-aroyl-4-phenyl-5-hydroxybenzofurans as a new class of antitubulin agentsRomeo Romagnoli, Pier Giovanni Baraldi, Taradas Sarkar, et al.
Bioorganic & Medicinal Chemistry Letters|March 10, 2007
Hybrid molecules containing benzo[4,5]imidazo[1,2-d][1,2,4]thiadiazole and alpha-bromoacryloyl moieties as potent apoptosis inducers on human myeloid leukaemia cellsRomeo Romagnoli, Pier Giovanni Baraldi, Maria Dora Carrion, et al.
Bioorganic & Medicinal Chemistry|February 14, 2012
7-Substituted-pyrrolo[3,2-d]pyrimidine-2,4-dione derivatives as antagonists of the transient receptor potential ankyrin 1 (TRPA1) channel: a promising approach for treating pain and inflammationPier Giovanni Baraldi, Romeo Romagnoli, Giulia Saponaro, et al.
Journal of Medicinal Chemistry|July 8, 2005
New pyrrolo[2,1-f]purine-2,4-dione and imidazo[2,1-f]purine-2,4-dione derivatives as potent and selective human A3 adenosine receptor antagonistsPier Giovanni Baraldi, Delia Preti, Mojgan Aghazadeh Tabrizi, et al.
Journal of Medicinal Chemistry|July 22, 2005
New 2-arylpyrazolo[4,3-c]quinoline derivatives as potent and selective human A3 adenosine receptor antagonistsPier Giovanni Baraldi, Mojgan Aghazadeh Tabrizi, Delia Preti, et al.
Bioconjugate Chemistry|August 29, 2019
Tetrabranched Hetero-Conjugated Peptides as Bifunctional Agonists of the NOP and Mu Opioid ReceptorsSalvatore Pacifico, Valentina Albanese, Davide Illuminati, et al.
Pageof 10