Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Chiara Brullo

Showing results (81-90 of 104) with videos related to

Pageof 11
Sort By:
Biochemistry|April 14, 2018
Molecular Bases of PDE4D Inhibition by Memory-Enhancing GEBR Library CompoundsTommaso Prosdocimi, Luca Mollica, Stefano Donini, et al.
Bioorganic & Medicinal Chemistry Letters|August 23, 2011
Identification of potent c-Src inhibitors strongly affecting the proliferation of human neuroblastoma cellsMarco Radi, Chiara Brullo, Emmanuele Crespan, et al.
Biochemical Pharmacology|July 11, 2025
Structure-guided combination of novel CFTR correctors to improve the function of F508del-CFTR in airway epithelial cellsDario Lunaccio, Caterina Allegretta, Emanuela Pesce, et al.
Journal of Medicinal Chemistry|November 11, 2005
Synthesis and 3D QSAR of new pyrazolo[3,4-b]pyridines: potent and selective inhibitors of A1 adenosine receptorsFabrizio Manetti, Silvia Schenone, Francesco Bondavalli, et al.
Molecules (Basel, Switzerland)|February 26, 2020
Insight into GEBR-32a: Chiral Resolution, Absolute Configuration and Enantiopreference in PDE4D InhibitionValeria Cavalloro, Katia Russo, Francesca Vasile, et al.
Journal of Medicinal Chemistry|July 5, 2007
Synthesis and biological evaluation of N-pyrazolyl-N'-alkyl/benzyl/phenylureas: a new class of potent inhibitors of interleukin 8-induced neutrophil chemotaxisOlga Bruno, Chiara Brullo, Francesco Bondavalli, et al.
Chemmedchem|July 2, 2013
Identification of Hck inhibitors as hits for the development of antileukemia and anti-HIV agentsCristina Tintori, Ilaria Laurenzana, Francesco La Rocca, et al.
Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics|May 17, 2024
Amelioration of functional and histopathological consequences after spinal cord injury through phosphodiesterase 4D (PDE4D) inhibitionMelissa Schepers, Sven Hendrix, Femke Mussen, et al.
Chemmedchem|March 14, 2008
Substituted pyrazolo[3,4-b]pyridines as potent A1 adenosine antagonists: synthesis, biological evaluation, and development of an A1 bovine receptor modelTiziano Tuccinardi, Silvia Schenone, Francesco Bondavalli, et al.
Journal of Medicinal Chemistry|February 9, 2008
Structure-based optimization of pyrazolo[3,4-d]pyrimidines as Abl inhibitors and antiproliferative agents toward human leukemia cell linesFabrizio Manetti, Chiara Brullo, Matteo Magnani, et al.
Pageof 11

Showing results (81-90 of 104) with videos related to

Sort By:
Pageof 11
Biochemistry|April 14, 2018
Molecular Bases of PDE4D Inhibition by Memory-Enhancing GEBR Library CompoundsTommaso Prosdocimi, Luca Mollica, Stefano Donini, et al.
Bioorganic & Medicinal Chemistry Letters|August 23, 2011
Identification of potent c-Src inhibitors strongly affecting the proliferation of human neuroblastoma cellsMarco Radi, Chiara Brullo, Emmanuele Crespan, et al.
Biochemical Pharmacology|July 11, 2025
Structure-guided combination of novel CFTR correctors to improve the function of F508del-CFTR in airway epithelial cellsDario Lunaccio, Caterina Allegretta, Emanuela Pesce, et al.
Journal of Medicinal Chemistry|November 11, 2005
Synthesis and 3D QSAR of new pyrazolo[3,4-b]pyridines: potent and selective inhibitors of A1 adenosine receptorsFabrizio Manetti, Silvia Schenone, Francesco Bondavalli, et al.
Molecules (Basel, Switzerland)|February 26, 2020
Insight into GEBR-32a: Chiral Resolution, Absolute Configuration and Enantiopreference in PDE4D InhibitionValeria Cavalloro, Katia Russo, Francesca Vasile, et al.
Journal of Medicinal Chemistry|July 5, 2007
Synthesis and biological evaluation of N-pyrazolyl-N'-alkyl/benzyl/phenylureas: a new class of potent inhibitors of interleukin 8-induced neutrophil chemotaxisOlga Bruno, Chiara Brullo, Francesco Bondavalli, et al.
Chemmedchem|July 2, 2013
Identification of Hck inhibitors as hits for the development of antileukemia and anti-HIV agentsCristina Tintori, Ilaria Laurenzana, Francesco La Rocca, et al.
Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics|May 17, 2024
Amelioration of functional and histopathological consequences after spinal cord injury through phosphodiesterase 4D (PDE4D) inhibitionMelissa Schepers, Sven Hendrix, Femke Mussen, et al.
Chemmedchem|March 14, 2008
Substituted pyrazolo[3,4-b]pyridines as potent A1 adenosine antagonists: synthesis, biological evaluation, and development of an A1 bovine receptor modelTiziano Tuccinardi, Silvia Schenone, Francesco Bondavalli, et al.
Journal of Medicinal Chemistry|February 9, 2008
Structure-based optimization of pyrazolo[3,4-d]pyrimidines as Abl inhibitors and antiproliferative agents toward human leukemia cell linesFabrizio Manetti, Chiara Brullo, Matteo Magnani, et al.
Pageof 11