RTU Zinātniskās darbības rezultāti un resursi: Personāls

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

Symmetric Molecules with 1,4-Triazole Moieties as Potent Inhibitors of Tumour-Associated Lactate Dehydrogenase-A
(2018)

Abdul-Malek Altamimi, Ahmed Alafeefy, Agnese Balode, Igor Vozny, Aleksandrs Pustenko, Mohey Eldin Shikh, Fatmah Alasmary, Sherif Abdel-Gawad, Raivis Žalubovskis
Zinātniskais raksts, kas indeksēts Web of science un/vai Scopus datu bāzē

Hydrophobic Substituents of the Phenylmethylsulfamide Moiety Can Be Used for the Development of New Selective Carbonic Anhydrase Inhibitors
(2014)

Jekaterīna Ivanova, Raivis Žalubovskis, Ginta Pizika, Simona Maria Monti, Giuseppina De Simone, Anna Di Fiore, Igor Vozny, Peteris Trapencieris, Claudiu T. Supuran, Vincenzo Alterio
Zinātniskais raksts, kas indeksēts Web of science un/vai Scopus datu bāzē

Synthesis of Triazolyl Derivatives of 2-Sulfonamido Thiophene
(2012)

Jekaterīna Ivanova, Agnese Balode, Raivis Žalubovskis, Aiga Grandane, Igor Vozny
Raksts konferenču tēžu krājumā

Synthesis of 6-Sulfamoylsaccharin and Study of Its Reactivity in Alkylation Reactions
(2012)

Jekaterīna Ivanova, Raivis Žalubovskis, Eriks Simins, Igor Vozny, Peteris Trapencieris
Zinātniskais raksts, kas indeksēts Web of science un/vai Scopus datu bāzē

Novel Method for the Preparation of 2h-1,2,4-Benzothiadiazin-3(4h)-One 1,1-Dioxides via a Curtius Rearrangement
(2012)

Jekaterīna Ivanova, Raivis Žalubovskis, Igor Vozny, Peteris Trapencieris, Diana Borovika
Zinātniskais raksts, kas indeksēts Web of science un/vai Scopus datu bāzē

Synthesis of an 8-Membered Heterocycle from Saccharin and Leakadine
(2012)

Jekaterīna Ivanova, Raivis Žalubovskis, Anatolijs Mišņovs, Igor Vozny, Gleb Kiselev
Zinātniskais raksts, kas indeksēts Web of science un/vai Scopus datu bāzē

Informācija par autoru

Publikācijas

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

Symmetric Molecules with 1,4-Triazole Moieties as Potent Inhibitors of Tumour-Associated Lactate Dehydrogenase-A
(2018)

Hydrophobic Substituents of the Phenylmethylsulfamide Moiety Can Be Used for the Development of New Selective Carbonic Anhydrase Inhibitors
(2014)

Synthesis of Triazolyl Derivatives of 2-Sulfonamido Thiophene
(2012)

Synthesis of 6-Sulfamoylsaccharin and Study of Its Reactivity in Alkylation Reactions
(2012)

Novel Method for the Preparation of 2h-1,2,4-Benzothiadiazin-3(4h)-One 1,1-Dioxides via a Curtius Rearrangement
(2012)

Synthesis of an 8-Membered Heterocycle from Saccharin and Leakadine
(2012)

Informācija par autoru

Publikācijas

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

Symmetric Molecules with 1,4-Triazole Moieties as Potent Inhibitors of Tumour-Associated Lactate Dehydrogenase-A (2018)

Hydrophobic Substituents of the Phenylmethylsulfamide Moiety Can Be Used for the Development of New Selective Carbonic Anhydrase Inhibitors (2014)

Synthesis of Triazolyl Derivatives of 2-Sulfonamido Thiophene (2012)

Synthesis of 6-Sulfamoylsaccharin and Study of Its Reactivity in Alkylation Reactions (2012)

Novel Method for the Preparation of 2h-1,2,4-Benzothiadiazin-3(4h)-One 1,1-Dioxides via a Curtius Rearrangement (2012)

Synthesis of an 8-Membered Heterocycle from Saccharin and Leakadine (2012)

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

Symmetric Molecules with 1,4-Triazole Moieties as Potent Inhibitors of Tumour-Associated Lactate Dehydrogenase-A
(2018)

Hydrophobic Substituents of the Phenylmethylsulfamide Moiety Can Be Used for the Development of New Selective Carbonic Anhydrase Inhibitors
(2014)

Synthesis of Triazolyl Derivatives of 2-Sulfonamido Thiophene
(2012)

Synthesis of 6-Sulfamoylsaccharin and Study of Its Reactivity in Alkylation Reactions
(2012)

Novel Method for the Preparation of 2h-1,2,4-Benzothiadiazin-3(4h)-One 1,1-Dioxides via a Curtius Rearrangement
(2012)

Synthesis of an 8-Membered Heterocycle from Saccharin and Leakadine
(2012)