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

Silvia Schenone

Showing results (131-140 of 173) with videos related to

Pageof 18
Sort By:
Journal of Chemical Information and Modeling|June 5, 2014
In silico identification and biological evaluation of novel selective serum/glucocorticoid-inducible kinase 1 inhibitors based on the pyrazolo-pyrimidine scaffoldFrancesco Ortuso, Rosario Amato, Anna Artese, et al.
Archiv Der Pharmazie|July 21, 2025
Design, Synthesis, In Vitro, and In Silico Studies of 5-(Diethylamino)-2-Formylphenyl Naphthalene-2-Sulfonate Based Thiosemicarbazones as Potent Anti-Alzheimer AgentsUrva Farooq, Muhammad Islam, Zahra Batool, et al.
Chemmedchem|March 16, 2012
Synthesis, biological activity, and ADME properties of novel S-DABOs/N-DABOs as HIV reverse transcriptase inhibitorsMarco Radi, Mafalda Pagano, Luigi Franchi, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|January 4, 2008
Antiproliferative and proapoptotic activities of new pyrazolo[3,4-d]pyrimidine derivative Src kinase inhibitors in human osteosarcoma cellsAdriano Spreafico, Silvia Schenone, Tommaso Serchi, 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.
Oncotarget|January 18, 2018
The small molecule SI113 synergizes with mitotic spindle poisons in arresting the growth of human glioblastoma multiformeClaudia Abbruzzese, Giada Catalogna, Enzo Gallo, 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.
Journal of Cellular Physiology|April 3, 2016
SRC Family Kinase Inhibition in Ewing Sarcoma Cells Induces p38 MAP Kinase-Mediated Cytotoxicity and Reduces Cell MigrationPaola Indovina, Nadia Casini, Iris Maria Forte, et al.
Bioorganic Chemistry|January 18, 2025
Design, synthesis, in-vitro and in-silico studies of novel N-heterocycle based hydrazones as α-glucosidase inhibitorsRehmatullah Farooqi, Saeed Ullah, Ajmal Khan, et al.
Pharmaceutics|November 27, 2024
Halloysite Nanotube-Based Delivery of Pyrazolo[3,4-<i>d</i>]pyrimidine Derivatives for Prostate and Bladder Cancer TreatmentMarina Massaro, Rebecca Ciani, Giancarlo Grossi, et al.
Pageof 18

Showing results (131-140 of 173) with videos related to

Sort By:
Pageof 18
Journal of Chemical Information and Modeling|June 5, 2014
In silico identification and biological evaluation of novel selective serum/glucocorticoid-inducible kinase 1 inhibitors based on the pyrazolo-pyrimidine scaffoldFrancesco Ortuso, Rosario Amato, Anna Artese, et al.
Archiv Der Pharmazie|July 21, 2025
Design, Synthesis, In Vitro, and In Silico Studies of 5-(Diethylamino)-2-Formylphenyl Naphthalene-2-Sulfonate Based Thiosemicarbazones as Potent Anti-Alzheimer AgentsUrva Farooq, Muhammad Islam, Zahra Batool, et al.
Chemmedchem|March 16, 2012
Synthesis, biological activity, and ADME properties of novel S-DABOs/N-DABOs as HIV reverse transcriptase inhibitorsMarco Radi, Mafalda Pagano, Luigi Franchi, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|January 4, 2008
Antiproliferative and proapoptotic activities of new pyrazolo[3,4-d]pyrimidine derivative Src kinase inhibitors in human osteosarcoma cellsAdriano Spreafico, Silvia Schenone, Tommaso Serchi, 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.
Oncotarget|January 18, 2018
The small molecule SI113 synergizes with mitotic spindle poisons in arresting the growth of human glioblastoma multiformeClaudia Abbruzzese, Giada Catalogna, Enzo Gallo, 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.
Journal of Cellular Physiology|April 3, 2016
SRC Family Kinase Inhibition in Ewing Sarcoma Cells Induces p38 MAP Kinase-Mediated Cytotoxicity and Reduces Cell MigrationPaola Indovina, Nadia Casini, Iris Maria Forte, et al.
Bioorganic Chemistry|January 18, 2025
Design, synthesis, in-vitro and in-silico studies of novel N-heterocycle based hydrazones as α-glucosidase inhibitorsRehmatullah Farooqi, Saeed Ullah, Ajmal Khan, et al.
Pharmaceutics|November 27, 2024
Halloysite Nanotube-Based Delivery of Pyrazolo[3,4-<i>d</i>]pyrimidine Derivatives for Prostate and Bladder Cancer TreatmentMarina Massaro, Rebecca Ciani, Giancarlo Grossi, et al.
Pageof 18