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

Stefania Ferro

Showing results (31-40 of 73) with videos related to

Pageof 8
Sort By:
Bioorganic & Medicinal Chemistry|March 13, 2014
A new potential approach to block HIV-1 replication via protein-protein interaction and strand-transfer inhibitionStefania Ferro, Laura De Luca, Giuseppa Lo Surdo, et al.
Archiv Der Pharmazie|June 15, 2007
New 4-[(1-benzyl-1H-indol-3-yl)carbonyl]-3-hydroxyfuran-2(5H)-ones, beta-diketo acid analogs as HIV-1 integrase inhibitorsStefania Ferro, Maria Letizia Barreca, Laura De Luca, et al.
Bioconjugate Chemistry|August 15, 2018
Graphene Quantum Dots Based Systems As HIV InhibitorsDaniela Iannazzo, Alessandro Pistone, Stefania Ferro, et al.
Bioorganic & Medicinal Chemistry|January 25, 2014
Design and synthesis of N₁-aryl-benzimidazoles 2-substituted as novel HIV-1 non-nucleoside reverse transcriptase inhibitorsAnna-Maria Monforte, Stefania Ferro, Laura De Luca, et al.
Bioorganic & Medicinal Chemistry Letters|April 18, 2008
A refined pharmacophore model for HIV-1 integrase inhibitors: Optimization of potency in the 1H-benzylindole seriesLaura De Luca, Maria Letizia Barreca, Stefania Ferro, et al.
Journal of Medicinal Chemistry|February 23, 2010
Identification of 3,4-Dihydroisoquinoline-2(1H)-sulfonamides as potent carbonic anhydrase inhibitors: synthesis, biological evaluation, and enzyme--ligand X-ray studiesRosaria Gitto, Stefano Agnello, Stefania Ferro, et al.
Bioorganic & Medicinal Chemistry|December 3, 2013
From NMDA receptor antagonists to discovery of selective σ₂ receptor ligandsRosaria Gitto, Laura De Luca, Stefania Ferro, et al.
Biomolecules|May 27, 2023
Epitope-Specific Anti-SerpinB3 Antibodies for SerpinB3 Recognition and Biological Activity InhibitionAlessandra Biasiolo, Michele Sandre, Stefania Ferro, et al.
Journal of Medicinal Chemistry|November 13, 2012
Synthesis and biological characterization of 3-substituted 1H-indoles as ligands of GluN2B-containing N-methyl-D-aspartate receptors. Part 2Rosaria Gitto, Laura De Luca, Stefania Ferro, et al.
Journal of Medicinal Chemistry|December 25, 2008
Docking studies on a new human immunodeficiency virus integrase-Mg-DNA complex: phenyl ring exploration and synthesis of 1H-benzylindole derivatives through fluorine substitutionsStefania Ferro, Laura De Luca, Maria Letizia Barreca, et al.
Pageof 8

Showing results (31-40 of 73) with videos related to

Sort By:
Pageof 8
Bioorganic & Medicinal Chemistry|March 13, 2014
A new potential approach to block HIV-1 replication via protein-protein interaction and strand-transfer inhibitionStefania Ferro, Laura De Luca, Giuseppa Lo Surdo, et al.
Archiv Der Pharmazie|June 15, 2007
New 4-[(1-benzyl-1H-indol-3-yl)carbonyl]-3-hydroxyfuran-2(5H)-ones, beta-diketo acid analogs as HIV-1 integrase inhibitorsStefania Ferro, Maria Letizia Barreca, Laura De Luca, et al.
Bioconjugate Chemistry|August 15, 2018
Graphene Quantum Dots Based Systems As HIV InhibitorsDaniela Iannazzo, Alessandro Pistone, Stefania Ferro, et al.
Bioorganic & Medicinal Chemistry|January 25, 2014
Design and synthesis of N₁-aryl-benzimidazoles 2-substituted as novel HIV-1 non-nucleoside reverse transcriptase inhibitorsAnna-Maria Monforte, Stefania Ferro, Laura De Luca, et al.
Bioorganic & Medicinal Chemistry Letters|April 18, 2008
A refined pharmacophore model for HIV-1 integrase inhibitors: Optimization of potency in the 1H-benzylindole seriesLaura De Luca, Maria Letizia Barreca, Stefania Ferro, et al.
Journal of Medicinal Chemistry|February 23, 2010
Identification of 3,4-Dihydroisoquinoline-2(1H)-sulfonamides as potent carbonic anhydrase inhibitors: synthesis, biological evaluation, and enzyme--ligand X-ray studiesRosaria Gitto, Stefano Agnello, Stefania Ferro, et al.
Bioorganic & Medicinal Chemistry|December 3, 2013
From NMDA receptor antagonists to discovery of selective σ₂ receptor ligandsRosaria Gitto, Laura De Luca, Stefania Ferro, et al.
Biomolecules|May 27, 2023
Epitope-Specific Anti-SerpinB3 Antibodies for SerpinB3 Recognition and Biological Activity InhibitionAlessandra Biasiolo, Michele Sandre, Stefania Ferro, et al.
Journal of Medicinal Chemistry|November 13, 2012
Synthesis and biological characterization of 3-substituted 1H-indoles as ligands of GluN2B-containing N-methyl-D-aspartate receptors. Part 2Rosaria Gitto, Laura De Luca, Stefania Ferro, et al.
Journal of Medicinal Chemistry|December 25, 2008
Docking studies on a new human immunodeficiency virus integrase-Mg-DNA complex: phenyl ring exploration and synthesis of 1H-benzylindole derivatives through fluorine substitutionsStefania Ferro, Laura De Luca, Maria Letizia Barreca, et al.
Pageof 8