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

Marta Ferraroni

Showing results (71-80 of 112) with videos related to

Pageof 12
Sort By:
Acta Crystallographica. Section D, Biological Crystallography|May 31, 2002
4-Chlorocatechol 1,2-dioxygenase from the chlorophenol-utilizing Gram-positive Rhodococcus opacus 1CP: crystallization and preliminary crystallographic analysisMarta Ferraroni, Maria Yolanda Ruiz Tarifa, Fabrizio Briganti, et al.
Dalton Transactions (Cambridge, England : 2003)|November 1, 2018
Interaction of a gold(i) dicarbene anticancer drug with human telomeric DNA G-quadruplex: solution and computationally aided X-ray diffraction analysisFederica Guarra, Tiziano Marzo, Marta Ferraroni, et al.
Bioorganic & Medicinal Chemistry|January 27, 2005
Diphenylcyclohexylamine derivatives as new potent multidrug resistance (MDR) modulatorsSilvia Dei, Roberta Budriesi, Paiwan Sudwan, et al.
Chemistry, an Asian Journal|February 12, 2016
Solution and Solid-State Analysis of Binding of 13-Substituted Berberine Analogues to Human Telomeric G-quadruplexesMarta Ferraroni, Carla Bazzicalupi, Francesco Papi, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|December 9, 2021
Calixarenes Incorporating Sulfonamide Moieties: Versatile Ligands for Carbonic Anhydrases InhibitionDavide Sbravati, Alessandro Bonardi, Silvia Bua, et al.
Bioorganic & Medicinal Chemistry|February 7, 2016
Sulfonamide inhibition studies of the β-carbonic anhydrase from the pathogenic bacterium Vibrio choleraeSonia Del Prete, Daniela Vullo, Viviana De Luca, et al.
Molecules (Basel, Switzerland)|May 16, 2020
Crystal Structure of a Tetrameric Type II β-Carbonic Anhydrase from the Pathogenic Bacterium <i>Burkholderia pseudomallei</i>Andrea Angeli, Marta Ferraroni, Mariana Pinteala, et al.
RSC Medicinal Chemistry|February 12, 2025
X-ray crystallographic and kinetic studies of biguanide containing aryl sulfonamides as carbonic anhydrase inhibitorsChiara Baroni, Murat Bozdag, Gioele Renzi, et al.
ACS Medicinal Chemistry Letters|October 16, 2024
Lasamide, a Potent Human Carbonic Anhydrase Inhibitor from the Market: Inhibition Profiling and Crystallographic StudiesChiara Baroni, Ilaria D'Agostino, Gioele Renzi, et al.
Bioorganic & Medicinal Chemistry|June 24, 2003
Synthesis and cholinergic affinity of diastereomeric and enantiomeric isomers of 1-methyl-2-(2-methyl-1,3-dioxolan-4-yl)- pyrrolidine, 1-methyl-2-(2-methyl-1,3-oxathiolan-5-yl)pyrrolidine and of Their iodomethylatesSilvia Dei, Cristina Bellucci, Michela Buccioni, et al.
Pageof 12

Showing results (71-80 of 112) with videos related to

Sort By:
Pageof 12
Acta Crystallographica. Section D, Biological Crystallography|May 31, 2002
4-Chlorocatechol 1,2-dioxygenase from the chlorophenol-utilizing Gram-positive Rhodococcus opacus 1CP: crystallization and preliminary crystallographic analysisMarta Ferraroni, Maria Yolanda Ruiz Tarifa, Fabrizio Briganti, et al.
Dalton Transactions (Cambridge, England : 2003)|November 1, 2018
Interaction of a gold(i) dicarbene anticancer drug with human telomeric DNA G-quadruplex: solution and computationally aided X-ray diffraction analysisFederica Guarra, Tiziano Marzo, Marta Ferraroni, et al.
Bioorganic & Medicinal Chemistry|January 27, 2005
Diphenylcyclohexylamine derivatives as new potent multidrug resistance (MDR) modulatorsSilvia Dei, Roberta Budriesi, Paiwan Sudwan, et al.
Chemistry, an Asian Journal|February 12, 2016
Solution and Solid-State Analysis of Binding of 13-Substituted Berberine Analogues to Human Telomeric G-quadruplexesMarta Ferraroni, Carla Bazzicalupi, Francesco Papi, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|December 9, 2021
Calixarenes Incorporating Sulfonamide Moieties: Versatile Ligands for Carbonic Anhydrases InhibitionDavide Sbravati, Alessandro Bonardi, Silvia Bua, et al.
Bioorganic & Medicinal Chemistry|February 7, 2016
Sulfonamide inhibition studies of the β-carbonic anhydrase from the pathogenic bacterium Vibrio choleraeSonia Del Prete, Daniela Vullo, Viviana De Luca, et al.
Molecules (Basel, Switzerland)|May 16, 2020
Crystal Structure of a Tetrameric Type II β-Carbonic Anhydrase from the Pathogenic Bacterium <i>Burkholderia pseudomallei</i>Andrea Angeli, Marta Ferraroni, Mariana Pinteala, et al.
RSC Medicinal Chemistry|February 12, 2025
X-ray crystallographic and kinetic studies of biguanide containing aryl sulfonamides as carbonic anhydrase inhibitorsChiara Baroni, Murat Bozdag, Gioele Renzi, et al.
ACS Medicinal Chemistry Letters|October 16, 2024
Lasamide, a Potent Human Carbonic Anhydrase Inhibitor from the Market: Inhibition Profiling and Crystallographic StudiesChiara Baroni, Ilaria D'Agostino, Gioele Renzi, et al.
Bioorganic & Medicinal Chemistry|June 24, 2003
Synthesis and cholinergic affinity of diastereomeric and enantiomeric isomers of 1-methyl-2-(2-methyl-1,3-dioxolan-4-yl)- pyrrolidine, 1-methyl-2-(2-methyl-1,3-oxathiolan-5-yl)pyrrolidine and of Their iodomethylatesSilvia Dei, Cristina Bellucci, Michela Buccioni, et al.
Pageof 12