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Bioorganic & Medicinal Chemistry
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February 10, 2009
Carbonic anhydrase inhibitors. The nematode alpha-carbonic anhydrase of Caenorhabditis elegans CAH-4b is highly inhibited by 2-(hydrazinocarbonyl)-3-substituted-phenyl-1H-indole-5-sulfonamides
Ozlen Güzel, Alessio Innocenti, Rebecca A Hall, et al.
Bioorganic & Medicinal Chemistry
|
September 30, 2008
Carbonic anhydrase inhibitors: synthesis and inhibition studies against mammalian isoforms I-XV with a series of 2-(hydrazinocarbonyl)-3-substituted-phenyl-1H-indole-5-sulfonamides
Ozlen Güzel, Alessio Innocenti, Andrea Scozzafava, et al.
Bioorganic & Medicinal Chemistry Letters
|
August 30, 2008
Carbonic anhydrase inhibitors: inhibition of the beta-class enzymes from the fungal pathogens Candida albicans and Cryptococcus neoformans with simple anions
Alessio Innocenti, Fritz A Mühlschlegel, Rebecca A Hall, et al.
Bioorganic & Medicinal Chemistry Letters
|
November 29, 2007
Carbonic anhydrase inhibitors: copper(II) complexes of polyamino-polycarboxylamido aromatic/heterocyclic sulfonamides are very potent inhibitors of the tumor-associated isoforms IX and XII
Marouan Rami, Jean-Yves Winum, Alessio Innocenti, et al.
Bioorganic & Medicinal Chemistry Letters
|
August 9, 2011
Synthesis of rhodamine B-benzenesulfonamide conjugates and their inhibitory activity against human α- and bacterial/fungal β-carbonic anhydrases
Marouan Rami, Alessio Innocenti, Jean-Louis Montero, et al.
Bioorganic & Medicinal Chemistry Letters
|
March 16, 2011
Carbonic anhydrase inhibitors. Inhibition of the β-class enzymes from the fungal pathogens Candida albicans and Cryptococcus neoformans with branched aliphatic/aromatic carboxylates and their derivatives
Fabrizio Carta, Alessio Innocenti, Rebecca A Hall, et al.
Bioorganic & Medicinal Chemistry Letters
|
August 21, 2012
Inhibition of α-class cytosolic human carbonic anhydrases I, II, IX and XII, and β-class fungal enzymes by carboxylic acids and their derivatives: new isoform-I selective nanomolar inhibitors
Mario Sechi, Alessio Innocenti, Nicolino Pala, et al.
Journal of Medicinal Chemistry
|
August 17, 2012
Carbamoylphosphonates control tumor cell proliferation and dissemination by simultaneously inhibiting carbonic anhydrase IX and matrix metalloproteinase-2. Toward nontoxic chemotherapy targeting tumor microenvironment
Reuven Reich, Amnon Hoffman, Ainelly Veerendhar, et al.
Journal of Medicinal Chemistry
|
October 1, 2004
Carbonic anhydrase inhibitors: the first on-resin screening of a 4-sulfamoylphenylthiourea library
Alessio Innocenti, Angela Casini, Maria C Alcaro, et al.
Bioorganic & Medicinal Chemistry Letters
|
February 3, 2005
Carbonic anhydrase inhibitors. Inhibition of the transmembrane isozyme XII with sulfonamides-a new target for the design of antitumor and antiglaucoma drugs?
Daniela Vullo, Alessio Innocenti, Isao Nishimori, et al.
Page
of 14
Search research articles
Search
Showing results (71-80 of 140) with videos related to
Sort By:
Page
of 14
Bioorganic & Medicinal Chemistry
|
February 10, 2009
Carbonic anhydrase inhibitors. The nematode alpha-carbonic anhydrase of Caenorhabditis elegans CAH-4b is highly inhibited by 2-(hydrazinocarbonyl)-3-substituted-phenyl-1H-indole-5-sulfonamides
Ozlen Güzel, Alessio Innocenti, Rebecca A Hall, et al.
Bioorganic & Medicinal Chemistry
|
September 30, 2008
Carbonic anhydrase inhibitors: synthesis and inhibition studies against mammalian isoforms I-XV with a series of 2-(hydrazinocarbonyl)-3-substituted-phenyl-1H-indole-5-sulfonamides
Ozlen Güzel, Alessio Innocenti, Andrea Scozzafava, et al.
Bioorganic & Medicinal Chemistry Letters
|
August 30, 2008
Carbonic anhydrase inhibitors: inhibition of the beta-class enzymes from the fungal pathogens Candida albicans and Cryptococcus neoformans with simple anions
Alessio Innocenti, Fritz A Mühlschlegel, Rebecca A Hall, et al.
Bioorganic & Medicinal Chemistry Letters
|
November 29, 2007
Carbonic anhydrase inhibitors: copper(II) complexes of polyamino-polycarboxylamido aromatic/heterocyclic sulfonamides are very potent inhibitors of the tumor-associated isoforms IX and XII
Marouan Rami, Jean-Yves Winum, Alessio Innocenti, et al.
Bioorganic & Medicinal Chemistry Letters
|
August 9, 2011
Synthesis of rhodamine B-benzenesulfonamide conjugates and their inhibitory activity against human α- and bacterial/fungal β-carbonic anhydrases
Marouan Rami, Alessio Innocenti, Jean-Louis Montero, et al.
Bioorganic & Medicinal Chemistry Letters
|
March 16, 2011
Carbonic anhydrase inhibitors. Inhibition of the β-class enzymes from the fungal pathogens Candida albicans and Cryptococcus neoformans with branched aliphatic/aromatic carboxylates and their derivatives
Fabrizio Carta, Alessio Innocenti, Rebecca A Hall, et al.
Bioorganic & Medicinal Chemistry Letters
|
August 21, 2012
Inhibition of α-class cytosolic human carbonic anhydrases I, II, IX and XII, and β-class fungal enzymes by carboxylic acids and their derivatives: new isoform-I selective nanomolar inhibitors
Mario Sechi, Alessio Innocenti, Nicolino Pala, et al.
Journal of Medicinal Chemistry
|
August 17, 2012
Carbamoylphosphonates control tumor cell proliferation and dissemination by simultaneously inhibiting carbonic anhydrase IX and matrix metalloproteinase-2. Toward nontoxic chemotherapy targeting tumor microenvironment
Reuven Reich, Amnon Hoffman, Ainelly Veerendhar, et al.
Journal of Medicinal Chemistry
|
October 1, 2004
Carbonic anhydrase inhibitors: the first on-resin screening of a 4-sulfamoylphenylthiourea library
Alessio Innocenti, Angela Casini, Maria C Alcaro, et al.
Bioorganic & Medicinal Chemistry Letters
|
February 3, 2005
Carbonic anhydrase inhibitors. Inhibition of the transmembrane isozyme XII with sulfonamides-a new target for the design of antitumor and antiglaucoma drugs?
Daniela Vullo, Alessio Innocenti, Isao Nishimori, et al.
Page
of 14