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

Simona Maria Monti

Showing results (31-40 of 85) with videos related to

Pageof 9
Sort By:
Journal of Enzyme Inhibition and Medicinal Chemistry|August 22, 2019
Exploration of the residues modulating the catalytic features of human carbonic anhydrase XIII by a site-specific mutagenesis approachGiuseppina De Simone, Anna Di Fiore, Emanuela Truppo, et al.
International Journal of Molecular Sciences|May 26, 2018
The Crystal Structure of a hCA VII Variant Provides Insights into the Molecular Determinants Responsible for Its Catalytic BehaviorMartina Buonanno, Anna Di Fiore, Emma Langella, et al.
Journal of Medicinal Chemistry|September 8, 2009
Carbonic anhydrase inhibitors. Comparison of aliphatic sulfamate/bis-sulfamate adducts with isozymes II and IX as a platform for designing tight-binding, more isoform-selective inhibitorsRosa Maria Vitale, Vincenzo Alterio, Alessio Innocenti, et al.
Journal of Enzyme Inhibition and Medicinal Chemistry|June 18, 2016
Design, synthesis and biological evaluation of N-(5-methyl-isoxazol-3-yl/1,3,4-thiadiazol-2-yl)-4-(3-substitutedphenylureido) benzenesulfonamides as human carbonic anhydrase isoenzymes I, II, VII and XII inhibitorsChandra Bhushan Mishra, Shikha Kumari, Andrea Angeli, et al.
Chemical Communications (Cambridge, England)|June 24, 2020
2-Mercaptobenzoxazoles: a class of carbonic anhydrase inhibitors with a novel binding mode to the enzyme active siteMurat Bozdag, Claudiu T Supuran, Davide Esposito, et al.
European Journal of Medicinal Chemistry|July 18, 2018
Discovery of potent anti-convulsant carbonic anhydrase inhibitors: Design, synthesis, in vitro and in vivo appraisalChandra Bhushan Mishra, Shikha Kumari, Andrea Angeli, et al.
The Enzymes|October 8, 2025
Saccharomyces cerevesiae, Candida spp. and Cryptococcus neoformans β-CAsAnna Di Fiore, Martina Buonanno, Davide Esposito, et al.
Medicinal Research Reviews|April 11, 2018
Inhibition of carbonic anhydrase IX targets primary tumors, metastases, and cancer stem cells: Three for the price of oneClaudiu T Supuran, Vincenzo Alterio, Anna Di Fiore, et al.
Cellular and Molecular Life Sciences : CMLS|March 23, 2018
Biochemical, biophysical and molecular dynamics studies on the proteoglycan-like domain of carbonic anhydrase IXEmma Langella, Martina Buonanno, Daniela Vullo, et al.
Protein Science : a Publication of the Protein Society|November 24, 2017
Prosystemin, a prohormone that modulates plant defense barriers, is an intrinsically disordered proteinMartina Buonanno, Mariangela Coppola, Ilaria Di Lelio, et al.
Pageof 9

Showing results (31-40 of 85) with videos related to

Sort By:
Pageof 9
Journal of Enzyme Inhibition and Medicinal Chemistry|August 22, 2019
Exploration of the residues modulating the catalytic features of human carbonic anhydrase XIII by a site-specific mutagenesis approachGiuseppina De Simone, Anna Di Fiore, Emanuela Truppo, et al.
International Journal of Molecular Sciences|May 26, 2018
The Crystal Structure of a hCA VII Variant Provides Insights into the Molecular Determinants Responsible for Its Catalytic BehaviorMartina Buonanno, Anna Di Fiore, Emma Langella, et al.
Journal of Medicinal Chemistry|September 8, 2009
Carbonic anhydrase inhibitors. Comparison of aliphatic sulfamate/bis-sulfamate adducts with isozymes II and IX as a platform for designing tight-binding, more isoform-selective inhibitorsRosa Maria Vitale, Vincenzo Alterio, Alessio Innocenti, et al.
Journal of Enzyme Inhibition and Medicinal Chemistry|June 18, 2016
Design, synthesis and biological evaluation of N-(5-methyl-isoxazol-3-yl/1,3,4-thiadiazol-2-yl)-4-(3-substitutedphenylureido) benzenesulfonamides as human carbonic anhydrase isoenzymes I, II, VII and XII inhibitorsChandra Bhushan Mishra, Shikha Kumari, Andrea Angeli, et al.
Chemical Communications (Cambridge, England)|June 24, 2020
2-Mercaptobenzoxazoles: a class of carbonic anhydrase inhibitors with a novel binding mode to the enzyme active siteMurat Bozdag, Claudiu T Supuran, Davide Esposito, et al.
European Journal of Medicinal Chemistry|July 18, 2018
Discovery of potent anti-convulsant carbonic anhydrase inhibitors: Design, synthesis, in vitro and in vivo appraisalChandra Bhushan Mishra, Shikha Kumari, Andrea Angeli, et al.
The Enzymes|October 8, 2025
Saccharomyces cerevesiae, Candida spp. and Cryptococcus neoformans β-CAsAnna Di Fiore, Martina Buonanno, Davide Esposito, et al.
Medicinal Research Reviews|April 11, 2018
Inhibition of carbonic anhydrase IX targets primary tumors, metastases, and cancer stem cells: Three for the price of oneClaudiu T Supuran, Vincenzo Alterio, Anna Di Fiore, et al.
Cellular and Molecular Life Sciences : CMLS|March 23, 2018
Biochemical, biophysical and molecular dynamics studies on the proteoglycan-like domain of carbonic anhydrase IXEmma Langella, Martina Buonanno, Daniela Vullo, et al.
Protein Science : a Publication of the Protein Society|November 24, 2017
Prosystemin, a prohormone that modulates plant defense barriers, is an intrinsically disordered proteinMartina Buonanno, Mariangela Coppola, Ilaria Di Lelio, et al.
Pageof 9