У виданнях, включених до науковометричних баз

Lesya N. Saliyeva, Irina V. Diachenko, Ruslan I. Vas'kevich, Nataliia Yu. Slyvka, Mikhailo V. Vovk Imidazothiazoles and their hydrogenated analogs: methods of synthesis and biomedical potential // Chemistry of Heterocyclic Compounds. – 2020. – Vol. 56, No. 11, pp. 1394–1407. Impact Factor 1.519 (Scopus)

Lytvynchuk M.B. A convenient method of synthesis of 8-acyl-2,3,6,7-tetrahydro-5H-[1,3]thiazolo[3,2-c]pyrimidin-5-ones / Lytvynchuk M.B., Bentya A.V., Slyvka N.Yu, Rusanov E.B. // Chemistry of Heterocyclic Compounds, 2020, Vol. 56, No. 1 pp. 101-107. Impact Factor 1.519 (Scopus)

Lytvynchuk M.B. 2-Ylidene-1,3-thiazolidines and their nonhydrogenated analogs: methods of syntesis and chemical properties / Lytvynchuk M.B., Bentya A.V., Slyvka N.Yu, Vovk M.V. // Chemistry of Heterocyclic Compounds, 2020, Vol. 56, No. 9 pp. 1130-1145. Impact Factor 1.519 (Scopus)

Holota, S.М. Synthesis and In vivo evaluation of pyrazoline-thiazolidin-4-one hybrid Les-5581 as a potential non-steroidal anti-inflammatory agent / Holota, S.М., Derkach, H.О., Demchuk, I.L., (...) Slyvka, N.Yu., Nektegayev, I.O., Lesyk, R.B. // Biopolymers and Cell, 2019, Vol. 35 (6), 2019, P. 437-447. Impact Factor 0.44 (Scopus)

Slivka N. Electrophilic intramolecular cyclization of 1-(N-alkenyl)-6-methylpyrimidine-2,4-diones / Slivka N., Hevaza Y., Saliyeva L. // Chemistry & Chemical Technology. - 2018. - Vol. 12, No. 3, pp. 279-418. Impact Factor 0.47(Scopus)

Saliyeva L.M. Synthesis of spiro[imidazo[2,1-b][1,3]thiazole-6,3'-pyrrolidine] derivatives / Saliyeva L.M., Slyvka N.Yu. , Mel’nyk D.A., Rusanov E.B., Vas’kevich R.I., Vovk M.V. // Chemistry of Heterocyclic Compounds, 2018, Vol. 54, No. 2, pp. 130-137. ISSN 1573-8353. Impact Factor 1.519 (Scopus)

Lytvynchuk M.B. Synthesis and functionalization of 2-alkylidene-5-(bromomethyl)-2,3-dihydro-1, 3-thiazole derivatives Lytvynchuk M.B., Bentya A.V., Slyvka N.Yu, Vovk M.V. // Chemistry of Heterocyclic Compounds, 2018, Vol. 54, No. 5, pp. 559-567. ISSN 1573-8353. Impact Factor 1.519 (Scopus)

Saliyeva L.M. Unexpected aminolysis reaction of 2-methyl-2,3-dihidroimidazo[2,1-b][1,3]-thiazol-5(6Н)-one / Saliyeva L.M., Slyvka N.Yu., Vas’kevich R.I., Rusanov E.B., Vovk M.V. // Chemistry of Heterocyclic Compounds, 2018, Vol. 54, No. 9, pp. 902-904. ISSN 1573-8353. Impact Factor 1.519 (Scopus)

Lytvynchuk M.B. Halocyclization of Products of Allyl Isothiocyanate Addition to Acyclic Methylene Active Compounds / Lytvynchuk M.B., Bentya A.V., Slyvka N.Yu, Vovk M.V. // Russian Journal of Organic Chemistry, 2017, Vol. 53, No. 5, pp. 709–716. Impact Factor 0.751 (Scopus)

Mariia B. Litvinchuk, Anton V. Bentya, Lesya N. Saliyeva, Eduard B. Rusanov, Mykhailo V. Vovk Characteristic features of interaction between (5-methyl-1,3-thiazolidin-2-ylidene) ketones and tosyl azide // Chemistry of Heterocyclic Compounds. – 2020. – Vol. 56, No. 9, pp. 1230–1233. IF: 1.519 (Scopus)

O. V. Tsisar, L. V. Piskach, O. V. Parasyuk, L. P. Marushko, I. D. Olekseyuk, O. V. Zamuruyeva, P. Czaja, P. Karasiński, A. M. El-Naggar, A. A. Albassam, G. Lakshminarayana. Tl2S–Ga2S3–GeS2 glasses for optically operated laser third harmonic generation // J Mater Sci: Mater Electron – 2017. – Vol. 28. – № 24. – p.p. 19003–19009. DOI: 10.1007/s10854-017-7854-x IF: 2.220 (2019)

O.V. Tsisar, L.V. Piskach, L.P. Marushko, E.M. Kadykalo, G.L. Myronchuk, A. Makhnovetz, M. Denysyuk, A.H. Reshak, A.M. El-Naggar, A.A. Albassam, I.V. Kityk. Optical features of novel semiconducting crystals Tl1–xGa1–xSnxSe2 (x=0.05; 0.1) // Optik – 2020. – Vol. 206. – 163572 DOI: 10.1016/j.ijleo.2019.163572 IF: 2.187 (2019)

A. Cherkas, P. Eckl, F. Gueraud, O. Abrahamovych, V. Serhiyenko, O. Yatskevych, M. Pliatsko, S. Golota. Helicobacter pylori in sedentary men is linked to higher heart rate, sympathetic activity, and insulin resistance but not inflammation or oxidative stress // Croatian Medical Journal. –2016. –Vol. 57, № 2. – P. 141-150. (IF= 1.62 Scopus)

Andrii Lozynskyi, Sergii Golota, Borys Zimenkovsky, Dmytro Atamanyuk, Andrzej Gzella, and Roman Lesyk. Synthesis, anticancer and antiviral activities of novel thiopyrano[2,3-d]thiazole-6-carbaldehydes // Phosphorus, Sulfur, and Silicon and the Related Elements. – 2016. – Vol. 191, № 9. – P. 1245-1249. (IF= 0.78 Scopus)

S. Golota, I Sydorenko, R. Surma, O. Karpenko, A. Gzella, R. Lesyk. Facile one-pot synthesis of 5-aryl/heterylidene-2-(2-hydroxyethyl- and 3-hydroxypropylamino)-thiazol-4-ones via catalytic aminolysis // Synthetic Communications, Vol. 47 (11), - 2017, - P. 1071-1076. (IF= 1.44 Scopus)

A. Cherkas, S. Golota, F. Gueraud, Ch.Pichler, A. Nersesyan, O. Yatskevych, M. Pliatsko, P. Eckl, S. Knasmüller. A study of the role of oxidative stress and low-grade inflammation in development of Helicobacter pylori-induced insulin resistance in asymptomatic sedentary young men // Free Radical Biology and Medicine, Vol. 108, Suppl. 1, - 2017, - P. S76. (IF= 5.65 Scopus)

A. Cherkas, S. Golota, F. Gueraud, Ch.Pichler, A. Nersesyan, O. Abrahamovych, V. Krupak, V. Bugiichyk, O. Yatskevych, M. Pliatsko, P. Eckl, S. Knasmüller. A Helicobacter pylori-associated insulin resistance in asymptomatic sedentary young men does not correlate with inflammatory markers and urine levels of 8-iso-PGF2-α or 1, 4-dihydroxynonane mercapturic acid // Archives of Physiology and Biochemistry, Vol. 128 (3), 2018, - P. 275-285. (IF= 2.11 Scopus)

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. – Vol. 2018 (4), 2018, - M1022. (IF= 0.45 Scopus)

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 (IF= 3.92 Scopus)

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. (IF= 0.44 Scopus)

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. (IF= 0.44 Scopus)

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. (IF= 4.52 Scopus)

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 Oct 19:127616. doi: 10.1016/j.bmcl.2020.127616. (IF=2.572 Scopus)

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 (IF=3.267, Q1-Pharmaceutical Sciences; Q2-Organic Chemistry, Drug Discovery)

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. Biopolym. Cell. 2021; 37(1):33-45. http://dx.doi.org/10.7124/bc.000A4A. (IF= 0.44 Scopus)

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. Biopolym. Cell. 2021; 37(1):46-61. http://dx.doi.org/10.7124/bc.000A4B. (IF= 0.44 Scopus)

Ihor Kotsan, Oksana Rakovets, Olga Abramchuk, Ludmila Shvarts, Natalia Kozachuk, Oleksandr Zhuravlov, Alona Zhuravlova, Ludmila Goshko, Tetiana Kachynska, Maria Osyp, Yurii Osyp, Illya Kuznetsov Electrophysiological Features of Brain Electric Activity in Individuals with Different Social Behavior / Ihor Kotsan Oksana Rakovets, Olga Abramchuk, Ludmila Shvarts, Natalia Kozachuk, Oleksandr Zhuravlov, Alona Zhuravlova, Ludmila Goshko, Tetiana Kachynska, Maria Osyp, Yurii Osyp, Illya Kuznetsov RJPBCS, May-June 2019, Vol. 10, № 3, P 85-92. IF: 0,127 Scopus

Канюка О., Філяк Є., Осип Ю., Кулачковський О., Сибірна Н. Кількісні зміни основних компонентів еритроцитарної мембрани визначають архітектоніку клітини за умов нокауту гена pttg / Канюка О., Філяк Є., Осип Ю., Кулачковський О., Сибірна Н. Ukr. Biochem. J. – 2014. – Vol. 86, № 2. – P 41-49. IF: 0,214 Scopus

Geir Bjorklund, Maryam Dadar, Natalia Martins, Salvatore Chirumbolo, Bey Hing Goh, Kateryna Smetanina, Roman Lysiuk. Brief Challenges on Medicinal Plants: An Eye-Opening Look at Ageing-Related Disorders // Basic Clinical Pharmacology Toxicology. - Nordic Association for the Publication of BCPT (former Nordic Pharmacological Society). - 2018. - P.1-20. іF: 3.176

K.Smetanina. Peculiarities and Integration of the pharmaconutriciology Foundaion on the Pre- and Post-Graduate stage of Study // Biomedical Journal of Scientific & Technical Research (BJSTR). – Vol.11, Іssue 3: 2018: 8530-8531 iF: 0.548

K.Smetanina. Peculiarities of Implementation of the Concept of Providing Quality of Drugs in Ukraine // American journal of Biomedical Science & Research. – 2019. – Vol. 3, issue 6. P. 492-494 iF: 0,823

Kormosh Z.A., Savchuk T.I., Semenishin D.I., Suprunovich S.V., Kochubei V.V., Korolchuk S.I. Potentiometric Sensor for Analgin Determination in Pharmaceutical formulations // Methods and objects of chemical analysis, 2020, Vol. 15, No. 2, 66–72 (IF 0,31 Scopus)