RTU Zinātniskās darbības rezultāti un resursi: Personāls

Informācija par autoru

Vārds, Uzvārds:

Raivis Žalubovskis

Struktūrvienība:

(32300) Ķīmijas un ķīmijas tehnoloģijas institūts

Zinātniskais grāds:

Doktors

E-pasts:

Raivis.Zalubovskis(at)rtu.lv

Publikācijas

Atrasti 67 rezultāti tiek attēloti no 31 līdz 40.

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

Further Exploration of DVD-445 as a Lead Thioredoxin Reductase (TrxR) Inhibitor for Cancer Therapy: Optimization of Potency and Evaluation of Anticancer Potential
(2020)

Mirna Jovanovic, Daniil Zhukovsky, Ana Podolski-Renic, Raivis Žalubovskis, Dmitry Dar`in, Vladimir Sharoyko, Tatiana Tennikova, Milica Pešic, Mikhail Krasavin
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

Novel Electrophilic Amides Amenable by the Ugi Reaction Perturb Thioredoxin System via Thioredoxin Reductase 1 (TrxR1) Inhibition: Identification of DVD-445 as a New Lead Compound for Anticancer Therapy
(2019)

M. Jovanovic, D. Zhukovsky, A. Podolski-Renic, I. Domračeva, Raivis Žalubovskis, M. Sencanski, S. Glišic, V. Sharoyko, T. Tennikova, D. Dar`in, M. Pešic, M. Krasavin
Zinātniskais raksts, kas indeksēts Web of science un/vai Scopus datu bāzē

Inhibitors of Selected Bacterial Metalloenzymes
(2019)

Raivis Žalubovskis, J.-Y. Winum
Zinātniskais raksts, kas indeksēts Web of science un/vai Scopus datu bāzē

Metalloenzymes as Therapeutic Targets
(2019)

B. Richichi, G.A. Spyroulias, J.-Y. Winum, Raivis Žalubovskis
Zinātniskais raksts, kas indeksēts Web of science un/vai Scopus datu bāzē

Informācija par autoru

Publikācijas

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)

Further Exploration of DVD-445 as a Lead Thioredoxin Reductase (TrxR) Inhibitor for Cancer Therapy: Optimization of Potency and Evaluation of Anticancer Potential
(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)

Novel Electrophilic Amides Amenable by the Ugi Reaction Perturb Thioredoxin System via Thioredoxin Reductase 1 (TrxR1) Inhibition: Identification of DVD-445 as a New Lead Compound for Anticancer Therapy
(2019)

Inhibitors of Selected Bacterial Metalloenzymes
(2019)

Metalloenzymes as Therapeutic Targets
(2019)

Vadītie promocijas darbi

Jauna veida ogļskābes anhidrāžu inhibitoru sintēze
(2020)

Ogļskābes anhidrāžu un tioredoksīnreduktāzes inhibitoru kā potenciālo pretvēža savienojumu sintēze
(2017)

Projekti

Inovatīvu neiropātisko sāpju mazināšanas līdzekļu iegūšana
Citi

Informācija par autoru

Publikācijas

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)

Further Exploration of DVD-445 as a Lead Thioredoxin Reductase (TrxR) Inhibitor for Cancer Therapy: Optimization of Potency and Evaluation of Anticancer Potential (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)

Novel Electrophilic Amides Amenable by the Ugi Reaction Perturb Thioredoxin System via Thioredoxin Reductase 1 (TrxR1) Inhibition: Identification of DVD-445 as a New Lead Compound for Anticancer Therapy (2019)

Inhibitors of Selected Bacterial Metalloenzymes (2019)

Metalloenzymes as Therapeutic Targets (2019)

Vadītie promocijas darbi

Jauna veida ogļskābes anhidrāžu inhibitoru sintēze (2020)

Ogļskābes anhidrāžu un tioredoksīnreduktāzes inhibitoru kā potenciālo pretvēža savienojumu sintēze (2017)

Projekti

Inovatīvu neiropātisko sāpju mazināšanas līdzekļu iegūšana Citi

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)

Further Exploration of DVD-445 as a Lead Thioredoxin Reductase (TrxR) Inhibitor for Cancer Therapy: Optimization of Potency and Evaluation of Anticancer Potential
(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)

Novel Electrophilic Amides Amenable by the Ugi Reaction Perturb Thioredoxin System via Thioredoxin Reductase 1 (TrxR1) Inhibition: Identification of DVD-445 as a New Lead Compound for Anticancer Therapy
(2019)

Inhibitors of Selected Bacterial Metalloenzymes
(2019)

Metalloenzymes as Therapeutic Targets
(2019)

Jauna veida ogļskābes anhidrāžu inhibitoru sintēze
(2020)

Ogļskābes anhidrāžu un tioredoksīnreduktāzes inhibitoru kā potenciālo pretvēža savienojumu sintēze
(2017)

Inovatīvu neiropātisko sāpju mazināšanas līdzekļu iegūšana
Citi