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

Giovanni Maga

Showing results (161-170 of 214) with videos related to

Pageof 22
Sort By:
Molecules (Basel, Switzerland)|November 7, 2019
Synthesis and Antiviral Activity of Novel 1,3,4-Thiadiazole Inhibitors of DDX3XAnnalaura Brai, Stefania Ronzini, Valentina Riva, et al.
Biochemistry|July 13, 2005
Specific targeting of hepatitis C virus NS3 RNA helicase. Discovery of the potent and selective competitive nucleotide-mimicking inhibitor QU663Giovanni Maga, Sandra Gemma, Caterina Fattorusso, et al.
Journal of Medicinal Chemistry|May 26, 2006
Design, molecular modeling, synthesis, and anti-HIV-1 activity of new indolyl aryl sulfones. Novel derivatives of the indole-2-carboxamideRino Ragno, Antonio Coluccia, Giuseppe La Regina, 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.
Journal of Medicinal Chemistry|October 4, 2007
Synthesis and biological properties of novel 2-aminopyrimidin-4(3H)-ones highly potent against HIV-1 mutant strainsAntonello Mai, Marino Artico, Dante Rotili, et al.
Nucleic Acids Research|August 14, 2018
p15PAF binding to PCNA modulates the DNA sliding surfaceMatteo De March, Susana Barrera-Vilarmau, Emmanuele Crespan, et al.
Journal of Medicinal Chemistry|June 21, 2012
New nitrogen containing substituents at the indole-2-carboxamide yield high potent and broad spectrum indolylarylsulfone HIV-1 non-nucleoside reverse transcriptase inhibitorsGiuseppe La Regina, Antonio Coluccia, Andrea Brancale, et al.
European Journal of Medicinal Chemistry|August 11, 2019
Identification of a new family of pyrazolo[3,4-d]pyrimidine derivatives as multitarget Fyn-Blk-Lyn inhibitors active on B- and T-lymphoma cell linesAnna Lucia Fallacara, Raffaele Passannanti, Mattia Mori, et al.
Chemmedchem|February 26, 2013
A combination strategy to inhibit Pim-1: synergism between noncompetitive and ATP-competitive inhibitorsMattia Mori, Cristina Tintori, Robert Selwyne Arul Christopher, et al.
Chemmedchem|December 18, 2007
A multidisciplinary approach for the identification of novel HIV-1 non-nucleoside reverse transcriptase inhibitors: S-DABOCs and DAVPsMarco Radi, Chiara Falciani, Lorenzo Contemori, et al.
Pageof 22

Showing results (161-170 of 214) with videos related to

Sort By:
Pageof 22
Molecules (Basel, Switzerland)|November 7, 2019
Synthesis and Antiviral Activity of Novel 1,3,4-Thiadiazole Inhibitors of DDX3XAnnalaura Brai, Stefania Ronzini, Valentina Riva, et al.
Biochemistry|July 13, 2005
Specific targeting of hepatitis C virus NS3 RNA helicase. Discovery of the potent and selective competitive nucleotide-mimicking inhibitor QU663Giovanni Maga, Sandra Gemma, Caterina Fattorusso, et al.
Journal of Medicinal Chemistry|May 26, 2006
Design, molecular modeling, synthesis, and anti-HIV-1 activity of new indolyl aryl sulfones. Novel derivatives of the indole-2-carboxamideRino Ragno, Antonio Coluccia, Giuseppe La Regina, 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.
Journal of Medicinal Chemistry|October 4, 2007
Synthesis and biological properties of novel 2-aminopyrimidin-4(3H)-ones highly potent against HIV-1 mutant strainsAntonello Mai, Marino Artico, Dante Rotili, et al.
Nucleic Acids Research|August 14, 2018
p15PAF binding to PCNA modulates the DNA sliding surfaceMatteo De March, Susana Barrera-Vilarmau, Emmanuele Crespan, et al.
Journal of Medicinal Chemistry|June 21, 2012
New nitrogen containing substituents at the indole-2-carboxamide yield high potent and broad spectrum indolylarylsulfone HIV-1 non-nucleoside reverse transcriptase inhibitorsGiuseppe La Regina, Antonio Coluccia, Andrea Brancale, et al.
European Journal of Medicinal Chemistry|August 11, 2019
Identification of a new family of pyrazolo[3,4-d]pyrimidine derivatives as multitarget Fyn-Blk-Lyn inhibitors active on B- and T-lymphoma cell linesAnna Lucia Fallacara, Raffaele Passannanti, Mattia Mori, et al.
Chemmedchem|February 26, 2013
A combination strategy to inhibit Pim-1: synergism between noncompetitive and ATP-competitive inhibitorsMattia Mori, Cristina Tintori, Robert Selwyne Arul Christopher, et al.
Chemmedchem|December 18, 2007
A multidisciplinary approach for the identification of novel HIV-1 non-nucleoside reverse transcriptase inhibitors: S-DABOCs and DAVPsMarco Radi, Chiara Falciani, Lorenzo Contemori, et al.
Pageof 22