| DC Field | Value | Language |
|---|
| dc.contributor.author | Yeromina, Hanna | |
| dc.contributor.author | Demchenko, Nataliya | |
| dc.contributor.author | Kiz, Olga | |
| dc.contributor.author | Ieromina, Zinaida | |
| dc.contributor.author | Demchenko, Sergiy | |
| dc.date.accessioned | 2020-03-02T12:28:12Z | - |
| dc.date.available | 2020-03-02T12:28:12Z | - |
| dc.date.created | 2019-02-28 | |
| dc.date.issued | 2019-02-28 | |
| dc.identifier.citation | The Synthesis and Antimicrobial Properties of New 2-(R-Phenylimino)-1,3-thiazoline Derivatives Containing the N-Methylpiperazine Moiety / Hanna Yeromina, Nataliya Demchenko, Olga Kiz, Zinaida Ieromina, Sergiy Demchenko // Chemistry & Chemical Technology. — Lviv : Lviv Politechnic Publishing House, 2019. — Vol 13. — No 2. — P. 150–156. | |
| dc.identifier.uri | https://ena.lpnu.ua/handle/ntb/46470 | - |
| dc.description.abstract | На основі несиметричних тіосечовин синте-
зовані нові похідні N-(R`-феніл)-3-(4-метил-1-піперазиніл)-1,3-
тіазол-2(3H)-іміну за реакцією Ганча. Структуру цільових
компонентів підтверджено елементим аналізом та ЯМР
спектроскопією. Досліджено антимікробну активність похід-
них 1,3-тіазоліну з N-метилпіперазиновим фрагментом щодо
сульфатвідновлювальних бактерій штаму Desulfovibrio sp. М
4.1. Встановлено, що сполуки з галогензаміщеним та незаміще-
ним фенільним фрагментом в 4-му положенні тіазолінового
циклу виявляють виразну протимікробну активність. | |
| dc.description.abstract | New derivatives of N-(R-phenyl)-3-(4-methyl-
1-piperazinyl)-1,3-thiazole-2(3H)- imine with the medium
to high yields were synthesized by the Hantzsch reaction
in the ethanol medium. The structure of target compounds
was confirmed by elemental analysis and NMR
spectroscopy. The antimicrobial activity of 1,3-thiazoline
derivatives with the N-methylpiperazine moiety against
sulfate-reducing bacteria of Desulfovibrio sp. М.4.1 strain
was studied. It was found that substances containing the
halo- and unsubstituted phenyl fragment in the position 4
of the thiazoline cycle showed the potent antimicrobial activity. | |
| dc.format.extent | 150-156 | |
| dc.language.iso | en | |
| dc.publisher | Видавництво Львівської політехніки | |
| dc.publisher | Lviv Politechnic Publishing House | |
| dc.relation.ispartof | Chemistry & Chemical Technology, 2 (13), 2019 | |
| dc.relation.uri | https://doi.org/10.3987/COM-14-13123 | |
| dc.relation.uri | https://doi.org/10.1016/j.bmc.2005.04.017 | |
| dc.relation.uri | https://doi.org/10.2478/BF02476181 | |
| dc.relation.uri | https://doi.org/10.1016/j.bmcl.2004.08.035 | |
| dc.relation.uri | https://doi.org/10.1002/jhet.2551 | |
| dc.relation.uri | https://doi.org/10.1007/s00044-015-1369-x | |
| dc.relation.uri | https://doi.org/10.1016/j.ejmech.2008.12.005 | |
| dc.relation.uri | https://doi.org/10.1021/cc049854w | |
| dc.relation.uri | https://doi.org/10.1021/cc049811f | |
| dc.relation.uri | https://doi.org/10.1016/j.tet.2010.05.015 | |
| dc.relation.uri | https://doi.org/10.1039/P19870000639 | |
| dc.relation.uri | https://doi.org/10.1002/ejoc.200801270 | |
| dc.relation.uri | https://doi.org/10.1055/s-0029-1217993 | |
| dc.relation.uri | https://doi.org/10.1002/ejoc.200800901 | |
| dc.relation.uri | https://doi.org/10.1016/j.ejmech.2010.08.034 | |
| dc.relation.uri | https://doi.org/10.1021/jo070246n | |
| dc.relation.uri | https://doi.org/10.1016/S1010-6030(02)00008-4 | |
| dc.relation.uri | https://doi.org/10.1080/10426507.2012.736897 | |
| dc.relation.uri | https://doi.org/10.1021/jo1012509 | |
| dc.relation.uri | https://doi.org/10.1080/10426507.2016.1150277 | |
| dc.relation.uri | https://doi.org/10.3390/molecules21030232 | |
| dc.relation.uri | https://doi.org/10.1002/anie.201306231 | |
| dc.relation.uri | https://doi.org/10.1007/s10593-005-0200-x | |
| dc.relation.uri | https://doi.org/10.1135/cccc19961205 | |
| dc.subject | 2-(R-феніліміно)-1 | |
| dc.subject | 3-тіазолін | |
| dc.subject | N-метил-піперазин | |
| dc.subject | синтез Ганча | |
| dc.subject | антимікробна активність | |
| dc.subject | сульфат-відновлювальні бактерії | |
| dc.subject | 2-(R-phenylimino)-1 | |
| dc.subject | 3-thiazoline | |
| dc.subject | N-methylpiperazine | |
| dc.subject | Hantzsch synthesis | |
| dc.subject | antimicrobial activity | |
| dc.subject | sulfate-reducing bacteria | |
| dc.title | The Synthesis and Antimicrobial Properties of New 2-(R-Phenylimino)-1,3-thiazoline Derivatives Containing the N-Methylpiperazine Moiety | |
| dc.title.alternative | Синтез та властивості нових похідних 2-(R-феніліміно)-1,3-тіазоліну, що містять фрагмент N-метилпіперазину | |
| dc.type | Article | |
| dc.rights.holder | © Національний університет „Львівська політехніка“, 2019 | |
| dc.rights.holder | © Yeromina H., Demchenko N., Kiz O., Ieromina Z., Demchenko S., 2019 | |
| dc.contributor.affiliation | National University of Pharmacy | |
| dc.contributor.affiliation | Chernihiv National T.G. Shevchenko Pedagogical University | |
| dc.contributor.affiliation | National Academy of Medical Sciences | |
| dc.format.pages | 7 | |
| dc.identifier.citationen | The Synthesis and Antimicrobial Properties of New 2-(R-Phenylimino)-1,3-thiazoline Derivatives Containing the N-Methylpiperazine Moiety / Hanna Yeromina, Nataliya Demchenko, Olga Kiz, Zinaida Ieromina, Sergiy Demchenko // Chemistry & Chemical Technology. — Lviv : Lviv Politechnic Publishing House, 2019. — Vol 13. — No 2. — P. 150–156. | |
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| dc.relation.referencesen | 1. Pogrebova I., Kozlova I., Purish L., Sokolovs'kaM.:Naukovi Visti Nats. Tekhn. Univ. Ukrainy "Kyivsky Politekhnich. Institut", 2015, 6, 115. | |
| dc.relation.referencesen | 2. Andreyuk K., Kozlova I., Kopteva Zh. et al., Mikrobna Koroziya Pidzemnih Sporud. Naukova dumka, Kyiv 2005. | |
| dc.relation.referencesen | 3. Shiran J., Yahyazadeh A., Yamin B. et al., Heterocycles, 2015, 91, 123. https://doi.org/10.3987/COM-14-13123 | |
| dc.relation.referencesen | 4. Park I.-K., Lim C.-S., NamK.-D. et al.:Korean J. Pesticide Sci., 2006, 10, 149. | |
| dc.relation.referencesen | 5. LimJ.-S., HanM.-S., NamK.-D. et al.:Korean J. Pesticide Sci., 2009, 13, 63. | |
| dc.relation.referencesen | 6. Sondhi S., Singh N., Lahoti A. et al., Bioorg. Med. Chem., 2005, 13, 4291. https://doi.org/10.1016/j.bmc.2005.04.017 | |
| dc.relation.referencesen | 7. Sondhi S., Bhattacharjee G., Jameel R. et al., Cent. Eur. J. Chem., 2004, 2, 1. https://doi.org/10.2478/BF02476181 | |
| dc.relation.referencesen | 8. Terzioglu N., van Rijn R., Bakker R. et al., Bioorg. Med. Chem. Lett., 2004, 14, 5251. https://doi.org/10.1016/j.bmcl.2004.08.035 | |
| dc.relation.referencesen | 9. HearnM., Wang T., CynamonM., J. Heterocyclic Chem., 2017, 54, 720. https://doi.org/10.1002/jhet.2551 | |
| dc.relation.referencesen | 10. TahaM., Ismail N., JamilW. et al.:Med. Chem. Res., 2015, 24, 3166. https://doi.org/10.1007/s00044-015-1369-x | |
| dc.relation.referencesen | 11. Demirbasa A., Sahin D., Demirbas N., Karaoglu S., Eur. J.Med. Chem., 2009, 44, 2896. https://doi.org/10.1016/j.ejmech.2008.12.005 | |
| dc.relation.referencesen | 12. Bae S., Hahn H.-G., NamK.-D., J. Comb. Chem., 2005, 7, 7. https://doi.org/10.1021/cc049854w | |
| dc.relation.referencesen | 13. Bae S., Hahn H.-G., NamK.-D., J. Comb. Chem., 2005, 7, 826. https://doi.org/10.1021/cc049811f | |
| dc.relation.referencesen | 14. Shin D., Lee J., Hahn H.-G., Tetrahedron, 2010, 66, 5707. https://doi.org/10.1016/j.tet.2010.05.015 | |
| dc.relation.referencesen | 15. Bramley S., Dupplin V., Goberdhan D., Meakins G., J. Chem. Soc. Perkin Transact. 1, 1987, 1, 639. https://doi.org/10.1039/P19870000639 | |
| dc.relation.referencesen | 16. Vogel A., Tatchell A., Furnis B. et al.:Vogel’s Textbook of Practical Organic Chemistry, 5th edn. Prentice Hall, Pearson 2005. | |
| dc.relation.referencesen | 17. Nath J., Ghosh H., Yella R., Patel B., Eur. J. Org. Chem., 2009, 2009, 1849. https://doi.org/10.1002/ejoc.200801270 | |
| dc.relation.referencesen | 18. Ghosh H., Synlett, 2009, 17, 2882. https://doi.org/10.1055/s-0029-1217993 | |
| dc.relation.referencesen | 19. Ghosh H., Yella R., Nath J., Patel B., Eur. J. Org. Chem., 2008, 6189. https://doi.org/10.1002/ejoc.200800901 | |
| dc.relation.referencesen | 20. Khan I., Ali S., Hameed S. et al., Eur. J. Med. Chem., 2010, 45, 5200. https://doi.org/10.1016/j.ejmech.2010.08.034 | |
| dc.relation.referencesen | 21. Nath J., Ghosh H., Yella R., Patel B., Eur. J. Org. Chem., 2009, 2009, 1849. https://doi.org/10.1002/ejoc.200801270 | |
| dc.relation.referencesen | 22. Wong R., Dolman S., J. Org. Chem., 2007, 72, 3969. https://doi.org/10.1021/jo070246n | |
| dc.relation.referencesen | 23. HollerM., Campo L., Brandelli A., Stefani V., J. Photochem. Photobiol. A, 2002, 149, 217. https://doi.org/10.1016/S1010-6030(02)00008-4 | |
| dc.relation.referencesen | 24. Wróblewska A., Mlostoń G., Phosphorus Sulfur, 2013, 188, 509. https://doi.org/10.1080/10426507.2012.736897 | |
| dc.relation.referencesen | 25. Demchenko S., Yeromina H., Perekhoda L. et al., Pat. UA111015, Publ. Oct. 25, 2016. | |
| dc.relation.referencesen | 26. Demchenko S., Yeromina H., Perekhoda L. et al., Pat. UA121484, Publ. Dec. 11, 2017. | |
| dc.relation.referencesen | 27. Yeromina H., Koshova O., Shcherbinina V. et al., Pat. UA120509, Publ. Nov. 10, 2017. | |
| dc.relation.referencesen | 28. Yeromina H., Koshova O., Shcherbinina V. et al., Pat. UA120847, Publ. Nov. 27, 2017. | |
| dc.relation.referencesen | 29. Perekhoda L., Yeromina H., Drapak I. et al., SJMPS, 2017, 3, 55. | |
| dc.relation.referencesen | 30. ChoD., Parthasarathi R., Pimentel A. et al., J. Org. Chem., 2010, 75, 6549. https://doi.org/10.1021/jo1012509 | |
| dc.relation.referencesen | 31. Akbarzadeh A., Soleymani R., Taheri M., Karimi-Cheshmeh ali M.:Orient. J. Chem., 2012, 28, 153. | |
| dc.relation.referencesen | 32. Yurttaş L., Özkay Y., DuranM. et al., Phosphorus Sulfur, 2016, 191, 1166. https://doi.org/10.1080/10426507.2016.1150277 | |
| dc.relation.referencesen | 33. Yang Z., Huang N., Xu B. et al.:Molecules, 2016, 21, 232. https://doi.org/10.3390/molecules21030232 | |
| dc.relation.referencesen | 34. Chen J., Liu D., Butt N. et al., Angewandte Chemie Int. Edn., 2013, 52, 11632. https://doi.org/10.1002/anie.201306231 | |
| dc.relation.referencesen | 35. Demchenko N., Kurmakova I., Tretyak O.:Microbiologia i Biotechnologia, 2013, 4, 90. | |
| dc.relation.referencesen | 36. Ehorov N., Rukovodstvo k Praktycheskym Zaniatyiampo Microbyolohyy. Izd-voMHU, Moskva 1983. | |
| dc.relation.referencesen | 37. Demchenko A., YanchenkoV., Kisly V., LozinskiiM., Chem. Heterocycl. Compd., 2005, 41, 668. https://doi.org/10.1007/s10593-005-0200-x | |
| dc.relation.referencesen | 38. LudwigM., Stverka P., Collect. Czech. Chem. Commun., 1996, 61, 1205. https://doi.org/10.1135/cccc19961205 | |
| dc.citation.issue | 2 | |
| dc.citation.spage | 150 | |
| dc.citation.epage | 156 | |
| dc.coverage.placename | Львів | |
| dc.coverage.placename | Lviv | |
| Appears in Collections: | Chemistry & Chemical Technology. – 2019. – Vol. 13, No. 2
|
