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

Sandro Cosconati

Showing results (131-140 of 150) with videos related to

Pageof 15
Sort By:
Journal of Medicinal Chemistry|April 23, 2010
Novel N2-substituted pyrazolo[3,4-d]pyrimidine adenosine A3 receptor antagonists: inhibition of A3-mediated human glioblastoma cell proliferationSabrina Taliani, Concettina La Motta, Laura Mugnaini, et al.
Journal of Medicinal Chemistry|July 16, 2015
Deepening the Topology of the Translocator Protein Binding Site by Novel N,N-Dialkyl-2-arylindol-3-ylglyoxylamidesElisabetta Barresi, Agostino Bruno, Sabrina Taliani, et al.
Journal of Medicinal Chemistry|August 10, 2023
Identification of a Protein Arginine Methyltransferase 7 (PRMT7)/Protein Arginine Methyltransferase 9 (PRMT9) InhibitorAlessandra Feoli, Giulia Iannelli, Alessandra Cipriano, et al.
Journal of Medicinal Chemistry|January 20, 2012
3-aryl-[1,2,4]triazino[4,3-a]benzimidazol-4(10H)-one: a novel template for the design of highly selective A₂B adenosine receptor antagonistsSabrina Taliani, Isabella Pugliesi, Elisabetta Barresi, et al.
Journal of Medicinal Chemistry|September 19, 2017
Computer-Aided Identification and Lead Optimization of Dual Murine Double Minute 2 and 4 Binders: Structure-Activity Relationship Studies and Pharmacological ActivityMariateresa Giustiniano, Simona Daniele, Sveva Pelliccia, et al.
Nucleic Acids Research|December 8, 2016
SIRT6 interacts with TRF2 and promotes its degradation in response to DNA damageAngela Rizzo, Sara Iachettini, Erica Salvati, et al.
Plos One|May 10, 2014
Properly substituted analogues of BIX-01294 lose inhibition of G9a histone methyltransferase and gain selective anti-DNA methyltransferase 3A activityDante Rotili, Domenico Tarantino, Biagina Marrocco, et al.
European Journal of Medicinal Chemistry|August 31, 2015
Investigation of new 2-aryl substituted Benzothiopyrano[4,3-d]pyrimidines as kinase inhibitors targeting vascular endothelial growth factor receptor 2Silvia Salerno, Anna Maria Marini, Giacomo Fornaciari, et al.
RSC Medicinal Chemistry|November 8, 2024
Discovery of <i>N</i>-substituted-2-oxoindolin benzoylhydrazines as c-MET/SMO modulators in EGFRi-resistant non-small cell lung cancerStefano Tomassi, Benito Natale, Michele Roggia, et al.
Journal of Medicinal Chemistry|June 9, 2021
Quinolinonyl Non-Diketo Acid Derivatives as Inhibitors of HIV-1 Ribonuclease H and Polymerase Functions of Reverse TranscriptaseAntonella Messore, Angela Corona, Valentina Noemi Madia, et al.
Pageof 15

Showing results (131-140 of 150) with videos related to

Sort By:
Pageof 15
Journal of Medicinal Chemistry|April 23, 2010
Novel N2-substituted pyrazolo[3,4-d]pyrimidine adenosine A3 receptor antagonists: inhibition of A3-mediated human glioblastoma cell proliferationSabrina Taliani, Concettina La Motta, Laura Mugnaini, et al.
Journal of Medicinal Chemistry|July 16, 2015
Deepening the Topology of the Translocator Protein Binding Site by Novel N,N-Dialkyl-2-arylindol-3-ylglyoxylamidesElisabetta Barresi, Agostino Bruno, Sabrina Taliani, et al.
Journal of Medicinal Chemistry|August 10, 2023
Identification of a Protein Arginine Methyltransferase 7 (PRMT7)/Protein Arginine Methyltransferase 9 (PRMT9) InhibitorAlessandra Feoli, Giulia Iannelli, Alessandra Cipriano, et al.
Journal of Medicinal Chemistry|January 20, 2012
3-aryl-[1,2,4]triazino[4,3-a]benzimidazol-4(10H)-one: a novel template for the design of highly selective A₂B adenosine receptor antagonistsSabrina Taliani, Isabella Pugliesi, Elisabetta Barresi, et al.
Journal of Medicinal Chemistry|September 19, 2017
Computer-Aided Identification and Lead Optimization of Dual Murine Double Minute 2 and 4 Binders: Structure-Activity Relationship Studies and Pharmacological ActivityMariateresa Giustiniano, Simona Daniele, Sveva Pelliccia, et al.
Nucleic Acids Research|December 8, 2016
SIRT6 interacts with TRF2 and promotes its degradation in response to DNA damageAngela Rizzo, Sara Iachettini, Erica Salvati, et al.
Plos One|May 10, 2014
Properly substituted analogues of BIX-01294 lose inhibition of G9a histone methyltransferase and gain selective anti-DNA methyltransferase 3A activityDante Rotili, Domenico Tarantino, Biagina Marrocco, et al.
European Journal of Medicinal Chemistry|August 31, 2015
Investigation of new 2-aryl substituted Benzothiopyrano[4,3-d]pyrimidines as kinase inhibitors targeting vascular endothelial growth factor receptor 2Silvia Salerno, Anna Maria Marini, Giacomo Fornaciari, et al.
RSC Medicinal Chemistry|November 8, 2024
Discovery of <i>N</i>-substituted-2-oxoindolin benzoylhydrazines as c-MET/SMO modulators in EGFRi-resistant non-small cell lung cancerStefano Tomassi, Benito Natale, Michele Roggia, et al.
Journal of Medicinal Chemistry|June 9, 2021
Quinolinonyl Non-Diketo Acid Derivatives as Inhibitors of HIV-1 Ribonuclease H and Polymerase Functions of Reverse TranscriptaseAntonella Messore, Angela Corona, Valentina Noemi Madia, et al.
Pageof 15