RTU Zinātniskās darbības rezultāti un resursi: Personāls

Response to Perspectives on the Classical Enzyme Carbonic Anhydrase and the Search for Inhibitors
(2021)

Andrea Angeli, Fabrizio Carta, Alessio Nocentini, Jean-Yves Winum, Raivis Žalubovskis, valentina Onnis, Wagdy E. Eldehna, Clemente Capasso, Simone Carradori, William A. Donald, Shoukat Dedhar, Claudiu T. Supuran
Zinātniskais raksts, kas indeksēts Web of science un/vai Scopus datu bāzē

Carbonic Anhydrase Inhibitors Targeting Metabolism and Tumor Microenvironment
(2020)

Andrea Angeli, Fabrizio Carta, Alessio Nocentini, Jean-Yves Winum, Raivis Žalubovskis, Atilla Akdemir, valentina Onnis, Wagdy E. Eldehna, Clemente Capasso, Giuseppina De Simone, Simona Maria Monti, Simone Carradori, William A. Donald, Shoukat Dedhar, Claudiu T. Supuran
Zinātniskais raksts, kas indeksēts Web of science un/vai Scopus datu bāzē

Development of Oxathiino[6,5-b]pyridine 2,2-Dioxide Derivatives as Selective Inhibitors of Tumor-Related Carbonic Anhydrases IX and XII
(2020)

Aiga Grandane, Alessio Nocentini, Ilona Domračeva, Raivis Žalubovskis, Claudiu T. Supuran
Zinātniskais raksts, kas indeksēts Web of science un/vai Scopus datu bāzē

Benzoxepinones: A New Isoform-Selective Class of Tumor Associated Carbonic Anhydrase Inhibitors
(2020)

Aiga Grandane, Alessio Nocentini, Thomas Werner, Raivis Žalubovskis, Claudiu T. Supuran
Zinātniskais raksts, kas indeksēts Web of science un/vai Scopus datu bāzē

7-Acylamino-3H-1,2-benzoxathiepine 2,2-Dioxides as New Isoform-Selective Carbonic Anhydrase IX and XII Inhibitors
(2020)

Aleksandrs Pustenko, Alessio Nocentini, Anastasija Balašova, Mikhail Krasavin, Raivis Žalubovskis, Claudiu T. Supuran
Zinātniskais raksts, kas indeksēts Web of science un/vai Scopus datu bāzē

Sulfocoumarins as Dual Inhibitors of Human Carbonic Anhydrase Isoforms IX/XII and of Human Thioredoxin Reductase
(2020)

Mikhail Krasavin, Raivis Žalubovskis, Aiga Grandane, Ilona Domračeva, Petr Zhmurov, Claudiu T. Supuran
Zinātniskais raksts, kas indeksēts Web of science un/vai Scopus datu bāzē

The Antibiotic Furagin and Its Derivatives are Isoform-Selective Human Carbonic Anhydrase Inhibitors
(2020)

Aleksandrs Pustenko, Alessio Nocentini, Paola Gratteri, Alessandro Bonardi, Igor Vozny, Raivis Žalubovskis, Claudiu T. Supuran
Zinātniskais raksts, kas indeksēts Web of science un/vai Scopus datu bāzē

Combining Carbonic Anhydrase and Thioredoxin Reductase Inhibitory Motifs within a Single Molecule Dramatically Increases Its Cytotoxicity
(2020)

Mikhail Krasavin, Tatiana Sharonova, Vladimir Sharoyko, Daniil Zhukovsky, Stanislav Kalinin, Raivis Žalubovskis, Tatiana Tennikova, Claudiu T. Supuran
Zinātniskais raksts, kas indeksēts Web of science un/vai Scopus datu bāzē

5-Substituted-benzylsulfanyl-thiophene-2-sulfonamides with Effective Carbonic Anhydrase Inhibitory Activity: Solution and Crystallographic Investigations
(2017)

Jekaterīna Ivanova, Agnese Balode, Raivis Žalubovskis, Janis Leitans, Andris Kazaks, Daniela Vullo, Kaspars Tārs, Claudiu T. Supuran
Zinātniskais raksts, kas indeksēts Web of science un/vai Scopus datu bāzē

N-Substituted and Ring Opened Saccharin Derivatives Selectively Inhibit Transmembrane, Tumor-Associated Carbonic Anhydrases IX and XII
(2017)

Jekaterīna Ivanova, Fabrizio Carta, Daniela Vullo, Janis Leitans, Andris Kazaks, Kaspars Tārs, Raivis Žalubovskis, Claudiu T. Supuran
Zinātniskais raksts, kas indeksēts Web of science un/vai Scopus datu bāzē

Informācija par autoru

Publikācijas

Response to Perspectives on the Classical Enzyme Carbonic Anhydrase and the Search for Inhibitors
(2021)

Carbonic Anhydrase Inhibitors Targeting Metabolism and Tumor Microenvironment
(2020)

Development of Oxathiino[6,5-b]pyridine 2,2-Dioxide Derivatives as Selective Inhibitors of Tumor-Related Carbonic Anhydrases IX and XII
(2020)

Benzoxepinones: A New Isoform-Selective Class of Tumor Associated Carbonic Anhydrase Inhibitors
(2020)

7-Acylamino-3H-1,2-benzoxathiepine 2,2-Dioxides as New Isoform-Selective Carbonic Anhydrase IX and XII Inhibitors
(2020)

Sulfocoumarins as Dual Inhibitors of Human Carbonic Anhydrase Isoforms IX/XII and of Human Thioredoxin Reductase
(2020)

The Antibiotic Furagin and Its Derivatives are Isoform-Selective Human Carbonic Anhydrase Inhibitors
(2020)

Combining Carbonic Anhydrase and Thioredoxin Reductase Inhibitory Motifs within a Single Molecule Dramatically Increases Its Cytotoxicity
(2020)

5-Substituted-benzylsulfanyl-thiophene-2-sulfonamides with Effective Carbonic Anhydrase Inhibitory Activity: Solution and Crystallographic Investigations
(2017)

N-Substituted and Ring Opened Saccharin Derivatives Selectively Inhibit Transmembrane, Tumor-Associated Carbonic Anhydrases IX and XII
(2017)

Informācija par autoru

Publikācijas

Response to Perspectives on the Classical Enzyme Carbonic Anhydrase and the Search for Inhibitors (2021)

Carbonic Anhydrase Inhibitors Targeting Metabolism and Tumor Microenvironment (2020)

Development of Oxathiino[6,5-b]pyridine 2,2-Dioxide Derivatives as Selective Inhibitors of Tumor-Related Carbonic Anhydrases IX and XII (2020)

Benzoxepinones: A New Isoform-Selective Class of Tumor Associated Carbonic Anhydrase Inhibitors (2020)

7-Acylamino-3H-1,2-benzoxathiepine 2,2-Dioxides as New Isoform-Selective Carbonic Anhydrase IX and XII Inhibitors (2020)

Sulfocoumarins as Dual Inhibitors of Human Carbonic Anhydrase Isoforms IX/XII and of Human Thioredoxin Reductase (2020)

The Antibiotic Furagin and Its Derivatives are Isoform-Selective Human Carbonic Anhydrase Inhibitors (2020)

Combining Carbonic Anhydrase and Thioredoxin Reductase Inhibitory Motifs within a Single Molecule Dramatically Increases Its Cytotoxicity (2020)

5-Substituted-benzylsulfanyl-thiophene-2-sulfonamides with Effective Carbonic Anhydrase Inhibitory Activity: Solution and Crystallographic Investigations (2017)

N-Substituted and Ring Opened Saccharin Derivatives Selectively Inhibit Transmembrane, Tumor-Associated Carbonic Anhydrases IX and XII (2017)

Response to Perspectives on the Classical Enzyme Carbonic Anhydrase and the Search for Inhibitors
(2021)

Carbonic Anhydrase Inhibitors Targeting Metabolism and Tumor Microenvironment
(2020)

Development of Oxathiino[6,5-b]pyridine 2,2-Dioxide Derivatives as Selective Inhibitors of Tumor-Related Carbonic Anhydrases IX and XII
(2020)

Benzoxepinones: A New Isoform-Selective Class of Tumor Associated Carbonic Anhydrase Inhibitors
(2020)

7-Acylamino-3H-1,2-benzoxathiepine 2,2-Dioxides as New Isoform-Selective Carbonic Anhydrase IX and XII Inhibitors
(2020)

Sulfocoumarins as Dual Inhibitors of Human Carbonic Anhydrase Isoforms IX/XII and of Human Thioredoxin Reductase
(2020)

The Antibiotic Furagin and Its Derivatives are Isoform-Selective Human Carbonic Anhydrase Inhibitors
(2020)

Combining Carbonic Anhydrase and Thioredoxin Reductase Inhibitory Motifs within a Single Molecule Dramatically Increases Its Cytotoxicity
(2020)

5-Substituted-benzylsulfanyl-thiophene-2-sulfonamides with Effective Carbonic Anhydrase Inhibitory Activity: Solution and Crystallographic Investigations
(2017)

N-Substituted and Ring Opened Saccharin Derivatives Selectively Inhibit Transmembrane, Tumor-Associated Carbonic Anhydrases IX and XII
(2017)