Search research articles
Contact Us
Filters
Showing results (31-40 of 273) with videos related to
Page
of 28
Sort By:
Journal of Medicinal Chemistry
|
May 8, 2013
Xanthates and trithiocarbonates strongly inhibit carbonic anhydrases and show antiglaucoma effects in vivo
Fabrizio Carta, Atilla Akdemir, Andrea Scozzafava, et al.
Bioorganic & Medicinal Chemistry
|
June 7, 2012
Mono-/dihydroxybenzoic acid esters and phenol pyridinium derivatives as inhibitors of the mammalian carbonic anhydrase isoforms I, II, VII, IX, XII and XIV
Fabrizio Carta, Daniela Vullo, Alfonso Maresca, et al.
Future Medicinal Chemistry
|
October 10, 2023
State of the art of carbonic anhydrase activators
Francesco Fiorentino, Fabrizio Carta, Dante Rotili, et al.
Bioorganic Chemistry
|
September 4, 2020
Unconventional amino acids in medicinal chemistry: First report on taurine merged within carbonic anhydrase inhibitors
Özlem Akgül, Andrea Angeli, Daniela Vullo, et al.
Bioorganic & Medicinal Chemistry Letters
|
December 15, 2010
Inhibition of β-carbonic anhydrases with ureido-substituted benzenesulfonamides
Fabio Pacchiano, Fabrizio Carta, Daniela Vullo, et al.
Bioorganic & Medicinal Chemistry
|
October 4, 2015
Click-tailed coumarins with potent and selective inhibitory action against the tumor-associated carbonic anhydrases IX and XII
Alessio Nocentini, Fabrizio Carta, Mariangela Ceruso, et al.
Bioorganic & Medicinal Chemistry
|
June 18, 2013
7-Substituted-sulfocoumarins are isoform-selective, potent carbonic anhydrase II inhibitors
Muhammet Tanc, Fabrizio Carta, Murat Bozdag, et al.
Journal of Enzyme Inhibition and Medicinal Chemistry
|
February 13, 2015
7-Amino-3,4-dihydro-1H-quinolin-2-one, a compound similar to the substituted coumarins, inhibits α-carbonic anhydrases without hydrolysis of the lactam ring
Daniela Vullo, Semra Isik, Murat Bozdag, et al.
Bioorganic & Medicinal Chemistry
|
March 16, 2013
Structural effect of phenyl ring compared to thiadiazole based adamantyl-sulfonamides on carbonic anhydrase inhibition
Shyamasri Biswas, Fabrizio Carta, Andrea Scozzafava, et al.
Bioorganic & Medicinal Chemistry
|
September 24, 2009
Carbonic anhydrase inhibitors. Diazenylbenzenesulfonamides are potent and selective inhibitors of the tumor-associated isozymes IX and XII over the cytosolic isoforms I and II
Fabrizio Carta, Alfonso Maresca, Andrea Scozzafava, et al.
Page
of 28
Search research articles
Search
Showing results (31-40 of 273) with videos related to
Sort By:
Page
of 28
Journal of Medicinal Chemistry
|
May 8, 2013
Xanthates and trithiocarbonates strongly inhibit carbonic anhydrases and show antiglaucoma effects in vivo
Fabrizio Carta, Atilla Akdemir, Andrea Scozzafava, et al.
Bioorganic & Medicinal Chemistry
|
June 7, 2012
Mono-/dihydroxybenzoic acid esters and phenol pyridinium derivatives as inhibitors of the mammalian carbonic anhydrase isoforms I, II, VII, IX, XII and XIV
Fabrizio Carta, Daniela Vullo, Alfonso Maresca, et al.
Future Medicinal Chemistry
|
October 10, 2023
State of the art of carbonic anhydrase activators
Francesco Fiorentino, Fabrizio Carta, Dante Rotili, et al.
Bioorganic Chemistry
|
September 4, 2020
Unconventional amino acids in medicinal chemistry: First report on taurine merged within carbonic anhydrase inhibitors
Özlem Akgül, Andrea Angeli, Daniela Vullo, et al.
Bioorganic & Medicinal Chemistry Letters
|
December 15, 2010
Inhibition of β-carbonic anhydrases with ureido-substituted benzenesulfonamides
Fabio Pacchiano, Fabrizio Carta, Daniela Vullo, et al.
Bioorganic & Medicinal Chemistry
|
October 4, 2015
Click-tailed coumarins with potent and selective inhibitory action against the tumor-associated carbonic anhydrases IX and XII
Alessio Nocentini, Fabrizio Carta, Mariangela Ceruso, et al.
Bioorganic & Medicinal Chemistry
|
June 18, 2013
7-Substituted-sulfocoumarins are isoform-selective, potent carbonic anhydrase II inhibitors
Muhammet Tanc, Fabrizio Carta, Murat Bozdag, et al.
Journal of Enzyme Inhibition and Medicinal Chemistry
|
February 13, 2015
7-Amino-3,4-dihydro-1H-quinolin-2-one, a compound similar to the substituted coumarins, inhibits α-carbonic anhydrases without hydrolysis of the lactam ring
Daniela Vullo, Semra Isik, Murat Bozdag, et al.
Bioorganic & Medicinal Chemistry
|
March 16, 2013
Structural effect of phenyl ring compared to thiadiazole based adamantyl-sulfonamides on carbonic anhydrase inhibition
Shyamasri Biswas, Fabrizio Carta, Andrea Scozzafava, et al.
Bioorganic & Medicinal Chemistry
|
September 24, 2009
Carbonic anhydrase inhibitors. Diazenylbenzenesulfonamides are potent and selective inhibitors of the tumor-associated isozymes IX and XII over the cytosolic isoforms I and II
Fabrizio Carta, Alfonso Maresca, Andrea Scozzafava, et al.
Page
of 28