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European Journal of Medicinal Chemistry
|
April 18, 2021
Taurultams incorporating arylsulfonamide: First in vitro inhibition studies of α-, β- and γ-class Carbonic Anhydrases from Vibrio cholerae and Burkholderia pseudomallei
Ozlem Akgul, Andrea Angeli, Silvia Selleri, et al.
Organic & Biomolecular Chemistry
|
March 19, 2010
Searching for intermediates in Prins cyclisations: the 2-oxa-5-adamantyl carbocation
Roger W Alder, Fabrizio Carta, Christopher A Reed, et al.
European Journal of Medicinal Chemistry
|
November 7, 2019
Direct and straightforward access to substituted alkyl selenols as novel carbonic anhydrase inhibitors
Damiano Tanini, Antonella Capperucci, Marta Ferraroni, et al.
Archiv Der Pharmazie
|
August 14, 2025
Novel Taurinamide-Based Compounds as Carbonic Anhydrase Inhibitors
Ozlem Akgul, Gioele Renzi, Andrea Angeli, et al.
Current Medicinal Chemistry
|
June 23, 2018
State of the Art on Carbonic Anhydrase Modulators for Biomedical Purposes
Murat Bozdag, Abdulmalik Saleh Alfawaz Altamimi, Daniela Vullo, et al.
Bioorganic & Medicinal Chemistry
|
July 23, 2013
Carbonic anhydrase inhibitors: Synthesis and inhibition of the cytosolic mammalian carbonic anhydrase isoforms I, II and VII with benzene sulfonamides incorporating 4,5,6,7-tetrachlorophthalimide moiety
Kalyan K Sethi, Saurabh M Verma, Muhammet Tanç, et al.
Journal of Medicinal Chemistry
|
July 2, 2010
Polyamines inhibit carbonic anhydrases by anchoring to the zinc-coordinated water molecule
Fabrizio Carta, Claudia Temperini, Alessio Innocenti, et al.
Current Pharmaceutical Design
|
September 8, 2010
The β-carbonic anhydrases from Mycobacterium tuberculosis as drug targets
Isao Nishimori, Tomoko Minakuchi, Alfonso Maresca, et al.
Journal of Computational Chemistry
|
June 13, 2025
Development of a New AMBER Force Field for Cysteine and Histidine Cadmium-Binding Proteins and Its Validation Through QM/MM MD Simulations
Matteo Orlandi, Marina Macchiagodena, Piero Procacci, et al.
Chemical Communications (Cambridge, England)
|
January 6, 2012
Dithiocarbamates: a new class of carbonic anhydrase inhibitors. Crystallographic and kinetic investigations
Fabrizio Carta, Mayank Aggarwal, Alfonso Maresca, et al.
Page
of 28
Search research articles
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Showing results (51-60 of 273) with videos related to
Sort By:
Page
of 28
European Journal of Medicinal Chemistry
|
April 18, 2021
Taurultams incorporating arylsulfonamide: First in vitro inhibition studies of α-, β- and γ-class Carbonic Anhydrases from Vibrio cholerae and Burkholderia pseudomallei
Ozlem Akgul, Andrea Angeli, Silvia Selleri, et al.
Organic & Biomolecular Chemistry
|
March 19, 2010
Searching for intermediates in Prins cyclisations: the 2-oxa-5-adamantyl carbocation
Roger W Alder, Fabrizio Carta, Christopher A Reed, et al.
European Journal of Medicinal Chemistry
|
November 7, 2019
Direct and straightforward access to substituted alkyl selenols as novel carbonic anhydrase inhibitors
Damiano Tanini, Antonella Capperucci, Marta Ferraroni, et al.
Archiv Der Pharmazie
|
August 14, 2025
Novel Taurinamide-Based Compounds as Carbonic Anhydrase Inhibitors
Ozlem Akgul, Gioele Renzi, Andrea Angeli, et al.
Current Medicinal Chemistry
|
June 23, 2018
State of the Art on Carbonic Anhydrase Modulators for Biomedical Purposes
Murat Bozdag, Abdulmalik Saleh Alfawaz Altamimi, Daniela Vullo, et al.
Bioorganic & Medicinal Chemistry
|
July 23, 2013
Carbonic anhydrase inhibitors: Synthesis and inhibition of the cytosolic mammalian carbonic anhydrase isoforms I, II and VII with benzene sulfonamides incorporating 4,5,6,7-tetrachlorophthalimide moiety
Kalyan K Sethi, Saurabh M Verma, Muhammet Tanç, et al.
Journal of Medicinal Chemistry
|
July 2, 2010
Polyamines inhibit carbonic anhydrases by anchoring to the zinc-coordinated water molecule
Fabrizio Carta, Claudia Temperini, Alessio Innocenti, et al.
Current Pharmaceutical Design
|
September 8, 2010
The β-carbonic anhydrases from Mycobacterium tuberculosis as drug targets
Isao Nishimori, Tomoko Minakuchi, Alfonso Maresca, et al.
Journal of Computational Chemistry
|
June 13, 2025
Development of a New AMBER Force Field for Cysteine and Histidine Cadmium-Binding Proteins and Its Validation Through QM/MM MD Simulations
Matteo Orlandi, Marina Macchiagodena, Piero Procacci, et al.
Chemical Communications (Cambridge, England)
|
January 6, 2012
Dithiocarbamates: a new class of carbonic anhydrase inhibitors. Crystallographic and kinetic investigations
Fabrizio Carta, Mayank Aggarwal, Alfonso Maresca, et al.
Page
of 28