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

Alessio Innocenti

Showing results (1-10 of 140) with videos related to

Pageof 14
Sort By:
Bioorganic & Medicinal Chemistry Letters|September 14, 2010
Paraoxon, 4-nitrophenyl phosphate and acetate are substrates of α- but not of β-, γ- and ζ-carbonic anhydrasesAlessio Innocenti, Claudiu T Supuran
Bioorganic & Medicinal Chemistry Letters|February 9, 2010
Carbonic anhydrase inhibitors. Inhibition of transmembrane isoforms IX, XII, and XIV with less investigated anions including trithiocarbonate and dithiocarbamateAlessio Innocenti, Andrea Scozzafava, Claudiu T Supuran
Bioorganic & Medicinal Chemistry Letters|March 10, 2009
Carbonic anhydrase inhibitors. Inhibition of cytosolic isoforms I, II, III, VII and XIII with less investigated inorganic anionsAlessio Innocenti, Andrea Scozzafava, Claudiu T Supuran
Bioorganic & Medicinal Chemistry Letters|August 3, 2010
Carbonic anhydrase inhibitors. Antioxidant polyphenols effectively inhibit mammalian isoforms I-XVAlessio Innocenti, Ilhami Gülçin, Andrea Scozzafava, et al.
European Journal of Medicinal Chemistry|June 18, 2010
Carbonic anhydrase inhibitors. Regioselective synthesis of novel 1-substituted 1,4-dihydro-4-oxo-3-pyridinesulfonamides and their inhibition of the human cytosolic isozymes I and II and transmembrane cancer-associated isozymes IX and XIIZdzisław Brzozowski, Jarosław Sławiński, Alessio Innocenti, et al.
Bioorganic & Medicinal Chemistry Letters|January 25, 2005
Carbonic anhydrase inhibitors. Inhibition of isozymes I, II, IV, V, and IX with anions isosteric and isoelectronic with sulfate, nitrate, and carbonateAlessio Innocenti, Daniela Vullo, Andrea Scozzafava, et al.
Bioorganic & Medicinal Chemistry|September 9, 2008
Carbonic anhydrase activators: kinetic and X-ray crystallographic study for the interaction of D- and L-tryptophan with the mammalian isoforms I-XIVClaudia Temperini, Alessio Innocenti, Andrea Scozzafava, et al.
Bioorganic & Medicinal Chemistry Letters|February 5, 2008
Carbonic anhydrase inhibitors: interactions of phenols with the 12 catalytically active mammalian isoforms (CA I-XIV)Alessio Innocenti, Daniela Vullo, Andrea Scozzafava, et al.
Bioorganic & Medicinal Chemistry Letters|July 22, 2008
Carbonic anhydrase inhibitors. Interaction of the antitumor sulfamate EMD 486019 with twelve mammalian carbonic anhydrase isoforms: Kinetic and X-ray crystallographic studiesClaudia Temperini, Alessio Innocenti, Andrea Scozzafava, et al.
Mini Reviews in Medicinal Chemistry|February 18, 2004
Antiviral sulfonamide derivativesClaudiu T Supuran, Alessio Innocenti, Antonio Mastrolorenzo, et al.
Pageof 14

Showing results (1-10 of 140) with videos related to

Sort By:
Pageof 14
Bioorganic & Medicinal Chemistry Letters|September 14, 2010
Paraoxon, 4-nitrophenyl phosphate and acetate are substrates of α- but not of β-, γ- and ζ-carbonic anhydrasesAlessio Innocenti, Claudiu T Supuran
Bioorganic & Medicinal Chemistry Letters|February 9, 2010
Carbonic anhydrase inhibitors. Inhibition of transmembrane isoforms IX, XII, and XIV with less investigated anions including trithiocarbonate and dithiocarbamateAlessio Innocenti, Andrea Scozzafava, Claudiu T Supuran
Bioorganic & Medicinal Chemistry Letters|March 10, 2009
Carbonic anhydrase inhibitors. Inhibition of cytosolic isoforms I, II, III, VII and XIII with less investigated inorganic anionsAlessio Innocenti, Andrea Scozzafava, Claudiu T Supuran
Bioorganic & Medicinal Chemistry Letters|August 3, 2010
Carbonic anhydrase inhibitors. Antioxidant polyphenols effectively inhibit mammalian isoforms I-XVAlessio Innocenti, Ilhami Gülçin, Andrea Scozzafava, et al.
European Journal of Medicinal Chemistry|June 18, 2010
Carbonic anhydrase inhibitors. Regioselective synthesis of novel 1-substituted 1,4-dihydro-4-oxo-3-pyridinesulfonamides and their inhibition of the human cytosolic isozymes I and II and transmembrane cancer-associated isozymes IX and XIIZdzisław Brzozowski, Jarosław Sławiński, Alessio Innocenti, et al.
Bioorganic & Medicinal Chemistry Letters|January 25, 2005
Carbonic anhydrase inhibitors. Inhibition of isozymes I, II, IV, V, and IX with anions isosteric and isoelectronic with sulfate, nitrate, and carbonateAlessio Innocenti, Daniela Vullo, Andrea Scozzafava, et al.
Bioorganic & Medicinal Chemistry|September 9, 2008
Carbonic anhydrase activators: kinetic and X-ray crystallographic study for the interaction of D- and L-tryptophan with the mammalian isoforms I-XIVClaudia Temperini, Alessio Innocenti, Andrea Scozzafava, et al.
Bioorganic & Medicinal Chemistry Letters|February 5, 2008
Carbonic anhydrase inhibitors: interactions of phenols with the 12 catalytically active mammalian isoforms (CA I-XIV)Alessio Innocenti, Daniela Vullo, Andrea Scozzafava, et al.
Bioorganic & Medicinal Chemistry Letters|July 22, 2008
Carbonic anhydrase inhibitors. Interaction of the antitumor sulfamate EMD 486019 with twelve mammalian carbonic anhydrase isoforms: Kinetic and X-ray crystallographic studiesClaudia Temperini, Alessio Innocenti, Andrea Scozzafava, et al.
Mini Reviews in Medicinal Chemistry|February 18, 2004
Antiviral sulfonamide derivativesClaudiu T Supuran, Alessio Innocenti, Antonio Mastrolorenzo, et al.
Pageof 14