Анонім

Відмінності між версіями «Голота Сергій Миколайович»

Матеріал з wiki.vnu.edu.ua
нема опису редагування
Рядок 26: Рядок 26:
'''Holota S.''', Komykhov S., Sysak S., Gzella A., Cherkas A., Lesyk R. Synthesis, Characterization and In vitro Evaluation of Novel 5-Ene-thiazolo[3,2-b][1,2,4]triazole-6(5H)-ones as Possible Anticancer Agents. Molecules. 2021; 26(4):1162. https://doi.org/10.3390/molecules26041162<br />
'''Holota S.''', Komykhov S., Sysak S., Gzella A., Cherkas A., Lesyk R. Synthesis, Characterization and In vitro Evaluation of Novel 5-Ene-thiazolo[3,2-b][1,2,4]triazole-6(5H)-ones as Possible Anticancer Agents. Molecules. 2021; 26(4):1162. https://doi.org/10.3390/molecules26041162<br />
A. Lozynskyi, '''S. Holota''', I. Yushyn, O. Sabadakh, O. Karpenko, V. Novikov, R Lesyk, Synthesis and Biological Activity Evaluation of Polyfunctionalized Anthraquinonehydrazones. Letters in Drug Design & Discovery, 2021, 18: 199. https://doi.org/10.2174/1570180817999200802032844<br />
A. Lozynskyi, '''S. Holota''', I. Yushyn, O. Sabadakh, O. Karpenko, V. Novikov, R Lesyk, Synthesis and Biological Activity Evaluation of Polyfunctionalized Anthraquinonehydrazones. Letters in Drug Design & Discovery, 2021, 18: 199. https://doi.org/10.2174/1570180817999200802032844<br />
Drapak I.V., Zimenkovsky B.S., Slabyy M.V., Holota S.M., Perekhoda L.O., Yaremkevych R.V., Nektegayev I.O. Synthesis and diuretic activity of novel 5-amino-1,3,4-thiadiazole-2-thiol derivatives. Biopolymer & Cell. 2021; 37(1):33-45. http://dx.doi.org/10.7124/bc.000A4A<br />
Drapak I.V., Zimenkovsky B.S., Slabyy M.V., '''Holota S.M.''', Perekhoda L.O., Yaremkevych R.V., Nektegayev I.O. Synthesis and diuretic activity of novel 5-amino-1,3,4-thiadiazole-2-thiol derivatives. Biopolymer & Cell. 2021; 37(1):33-45. http://dx.doi.org/10.7124/bc.000A4A<br />
Holota S.M., Nektegayev I.O., Soronovych I.I., Chubuchna I.I., Kolishetska M.A., Sysak S.P., Regeda M.S., Lesyk R.B. The novel pyrazolin-5-one bearing thiazolidin-4-ones: synthesis, characterization and biological evaluation. Biopolymer & Cell. 2021; 37(1):46-61. http://dx.doi.org/10.7124/bc.000A4B<br />
'''Holota S.M.''', Nektegayev I.O., Soronovych I.I., Chubuchna I.I., Kolishetska M.A., Sysak S.P., Regeda M.S., Lesyk R.B. The novel pyrazolin-5-one bearing thiazolidin-4-ones: synthesis, characterization and biological evaluation. Biopolymer & Cell. 2021; 37(1):46-61. http://dx.doi.org/10.7124/bc.000A4B<br />
Schadich E, Kryshchyshyn-Dylevych A, Holota S, Polishchuk P, Džubak P, Gurska S, Hajduch M, Lesyk R. Assessing different thiazolidine and thiazole based compounds as antileishmanial scaffolds. Bioorg Med Chem Lett. 2020:127616. doi: 10.1016/j.bmcl.2020.127616.<br />
Schadich E, Kryshchyshyn-Dylevych A, '''Holota S''', Polishchuk P, Džubak P, Gurska S, Hajduch M, Lesyk R. Assessing different thiazolidine and thiazole based compounds as antileishmanial scaffolds. Bioorg Med Chem Lett. 2020:127616. https://doi:10.1016/j.bmcl.2020.127616.<br />
Cherkas, A., Holota, S., Mdzinarashvili, T., Gabbianelli, R., & Zarkovic, N. Glucose as a Major Antioxidant: When, What for and Why It Fails?. Antioxidants. 2020;9(2): 140. pii: E140. doi: 10.3390/antiox9020140.<br />
Cherkas, A., '''Holota, S.''', Mdzinarashvili, T., Gabbianelli, R., & Zarkovic, N. Glucose as a Major Antioxidant: When, What for and Why It Fails?. Antioxidants. 2020;9(2): 140. pii: E140. https://doi:10.3390/antiox9020140.<br />
Holota S. M., Derkach H. O., Demchuk I. L., Vynnytska R. B., Antoniv O. I., Furdychko L. O., Slyvka N. Yu., Nektegayev I. O., Lesyk R. B. Synthesis and in vivo evaluation of pyrazoline-thiazolidin-4-one hybrid Les-5581 as a potential non-steroidal anti-inflammatory agent. Biopolymer & Cell. 2019; 35(6):437-447. dx.doi.org/10.7124/bc.000A17.<br />
'''Holota S. M.''', Derkach H. O., Demchuk I. L., Vynnytska R. B., Antoniv O. I., Furdychko L. O., Slyvka N. Yu., Nektegayev I. O., Lesyk R. B. Synthesis and in vivo evaluation of pyrazoline-thiazolidin-4-one hybrid Les-5581 as a potential non-steroidal anti-inflammatory agent. Biopolymer & Cell. 2019; 35(6):437-447. https://dx.doi.org/10.7124/bc.000A17.<br />
Holota S. M., Derkach G. O., Zasidko V. V., Trokhymchuk V. V., Furdychko L. O., Demchuk I. L., Semenciv G. M., Soronovych I. I., Kutsyk R. V., Lesyk R. B. Features of antimicrobial activity of some 5-aminomethylene-2-thioxo-4-thiazolidinones. Biopolymer & Cell. 2019; 35(5):371-380. dx.doi.org/10.7124/bc.000A0E<br />
'''Holota S. M.''', Derkach G. O., Zasidko V. V., Trokhymchuk V. V., Furdychko L. O., Demchuk I. L., Semenciv G. M., Soronovych I. I., Kutsyk R. V., Lesyk R. B. Features of antimicrobial activity of some 5-aminomethylene-2-thioxo-4-thiazolidinones. Biopolymer & Cell. 2019; 35(5):371-380. https://dx.doi.org/10.7124/bc.000A0E<br />
Holota S, Kryshchyshyn A, Derkach H, Trufin Y, Demchuk I, Gzella A, Grellier Ph, Lesyk R. Synthesis of 5-enamine-4-thiazolidinone derivatives with trypanocidal and anticancer activity. Bioorganic Chemistry, 2019; 86:126-136. doi.org/10.1016/j.bioorg.2019.01.045<br />
'''Holota S''', Kryshchyshyn A, Derkach H, Trufin Y, Demchuk I, Gzella A, Grellier Ph, Lesyk R. Synthesis of 5-enamine-4-thiazolidinone derivatives with trypanocidal and anticancer activity. Bioorganic Chemistry, 2019; 86:126-136. https://doi.org/10.1016/j.bioorg.2019.01.045<br />
S. Holota, Ya. Shylych, H. Derkach, O. Karpenko, A. Gzella, R. Lesyk. Synthesis of 4-(2H-[1,2,4]-Triazol-5-ylsulfanyl)-1,2-dihydropyrazol-3-one via Ring-Switching Hydrazinolysis of 5-Ethoxymethylidenethiazolo[3,2-b][1,2,4]triazol-6-one // Molbank. 2018 (4), 2018, -M1022.  
'''S. Holota''', Ya. Shylych, H. Derkach, O. Karpenko, A. Gzella, R. Lesyk. Synthesis of 4-(2H-[1,2,4]-Triazol-5-ylsulfanyl)-1,2-dihydropyrazol-3-one via Ring-Switching Hydrazinolysis of 5-Ethoxymethylidenethiazolo[3,2-b][1,2,4]triazol-6-one // Molbank. 2018 (4), 2018, -M1022.  
doi.org/10.3390/M1022<br />
https://doi.org/10.3390/M1022<br />


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