Прогнозований скринінг біологічної активності S-алкілових естерів 8-хінолінтіосульфокислоти
dc.citation.epage | 134 | |
dc.citation.issue | 1 | |
dc.citation.spage | 125 | |
dc.contributor.affiliation | Національний університет “Львівська політехніка” | |
dc.contributor.affiliation | Lviv Polytechnic National University | |
dc.contributor.author | Стадницька, Н. Є. | |
dc.contributor.author | Монька, Н. Я. | |
dc.contributor.author | Губицька, І. І. | |
dc.contributor.author | Курка, М. С. | |
dc.contributor.author | Лубенець, В. І. | |
dc.contributor.author | Stadnytska, N. | |
dc.contributor.author | Monka, N. | |
dc.contributor.author | Hubytska, I. | |
dc.contributor.author | Kurka, M. | |
dc.contributor.author | Lubenets, V. | |
dc.coverage.placename | Lviv | |
dc.coverage.placename | Lviv | |
dc.date.accessioned | 2021-01-28T11:24:03Z | |
dc.date.available | 2021-01-28T11:24:03Z | |
dc.date.created | 2020-02-24 | |
dc.date.issued | 2020-02-24 | |
dc.description.abstract | Хінолін та його похідні є важливими сполуками для хімічного синтезу та розроблення на їх основі нових лікарських засобів. Відоме практичне застосування низки речовин із хіноліновим гетероциклом у медичній практиці. Виконано прогнозований скринінг біоло- гічної активності, цитотоксичності та токсичної дії на щурах синтезованих S-алкілових естерів 8-хінолінтіосульфокислоти з використанням відповідних online програм. Виявлено, що вони є малотоксичними речовинами з широким спектром біологічної дії та високим значенням ймовірності активності, що засвідчує доцільність продовження експерименталь- них досліджень їх властивостей. Особливої уваги заслуговують метиловий та етиловий естери 8-хінолінтіосульфокислоти. | |
dc.description.abstract | Quinoline and its derivatives are important compounds for the chemical synthesis and development of novel drugs. Practical application of a number of substances with quinoline heterocycle is already known in medical practice. We performed predictive screening for biological activity, cytotoxic and toxic effects on rats of synthesized 8-quinoline thiosulfonic acid S-alkyl esters using appropriate on-line programs. They have been found to be low-toxic substances with a broad spectrum of biological action and a high probability of activity, which indicates the expediency of continuing experimental studies of their properties. Particular attention should be paid to the methyl and ethyl esters of 8-quinolintiosulfonic acids. | |
dc.format.extent | 125-134 | |
dc.format.pages | 10 | |
dc.identifier.citation | Прогнозований скринінг біологічної активності S-алкілових естерів 8-хінолінтіосульфокислоти / Н. Є. Стадницька, Н. Я. Монька, І. І. Губицька, М. С. Курка, В. І. Лубенець // Chemistry, Technology and Application of Substances. — Lviv : Lviv Politechnic Publishing House, 2020. — Том 3. — № 1. — С. 125–134. | |
dc.identifier.citationen | Predictive screening of the biological activity of S-alkyl esters of 8-quinolinsulfonic acid / N. Stadnytska, N. Monka, I. Hubytska, M. Kurka, V. Lubenets // Chemistry, Technology and Application of Substances. — Lviv : Lviv Politechnic Publishing House, 2020. — Vol 3. — No 1. — P. 125–134. | |
dc.identifier.doi | doi.org/10.23939/ctas2020.01.125 | |
dc.identifier.uri | https://ena.lpnu.ua/handle/ntb/56073 | |
dc.language.iso | uk | |
dc.publisher | Lviv Politechnic Publishing House | |
dc.relation.ispartof | Chemistry, Technology and Application of Substances, 1 (3), 2020 | |
dc.relation.references | 1. Pietro O. D., Vicente-García E., Taylor M. C., Berenguer D., Viayna E., Lanzoni A., Sola I., Sayago H., Riera C., Fisa R., Clos M. V., Pérez B., Kelly J. M., Lavilla R., Muñoz-Torrero D. (2015) Multicomponent reaction-based synthesis and biological evaluation of tricyclic heterofusedquinolines with multi-trypanosomatid activity. European Journal of Medicinal Chemistry. 105, 120–137. | |
dc.relation.references | 2. Juan Carlos Coa, Wilson Castrillón, Wilson Cardona, Miguel Carda, Victoria Ospina, July Andrea Muñoz, Iván D. Vélez, Sara M. Robledo. (2015) Synthesis, leishmanicidal, trypanocidal and cytotoxic activity of quinoline-hydrazone hybrids. European Journal of Medicinal Chemistry, 101, 746–753. | |
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dc.relation.references | 6. Cziaky Z., Korodi F., Frank L and Czink I. (1996). Synthesis and antimycotic activity of new 2-chloro-3-(2- nitro)ethyl- and (2-nitro)vlnylquinolines. Heterocyclic Communications, 2(1), 63–70. | |
dc.relation.references | 7. Delgado J. N., Remers W. A. Wilson and Gisvold’s (1998). Text Book of Organic Medicinal and Pharmaceutical Chemistry, 10 th ed. Lippincott Williams & Wilkins. Text Book, 235–252. | |
dc.relation.references | 8. Farghally A. M., Habib N. S., Hazzaa A. A. B. and El-Sayed O. A. (1985). Synthesis of substituted quinoline-3-carbaldehyde (2,3-dihydrothiazol-2-ylidene) hydrazones of potential antimicrobial activity. Journal de Pharmacie de Belgique, 40(6), 366–372. | |
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dc.relation.references | 10. Bekhit A. A., El-Sayed O. A., Aboulmagd E., Park J. Y. (2004). Tetrazolo[1,5-a]quinoline as a potential promising new scaffold for the synthesis of novel anti-infl ammatory and antibacterial agents. Eur. J. Med. Chem, 39(3), 249–255. | |
dc.relation.references | 11. Gupta R., Gupta A. K., Paul S. and Kachroo P. L. (1998). Synthesis and biological activities of some 2- chloro-6/8-substituted-3-(3-alkyl/aryl-5,6-dihydro-s-triazolo [3,4-b][1,3,4]thiadiazol-6-yl)quinolines. Indian Journal Of Chemistry B., 37, 1211–1213. | |
dc.relation.references | 12. Nicolaou K. C., Gross J. L., Kerr M. A. (1996). Synthesis of novel heterocycles related to the Dynemicin A ring skeleton. J. Heterocycl. Chem. 33(3), 735–746. | |
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dc.relation.references | 15. Kuz’menko L., Avdeenko A., Konovalova S., Vasylyuk S., Fedorova O., Monka N., Krychkovska A., Lubenets V. (2019). Synthesis and study of pesticidal activity of some N-arylthio-1,4-benzoquinone imines. Biointerface Research in Applied Chemistry. 9(5), 4232 –4238. | |
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dc.relation.references | 17.Mampuys P.,McElroy C. R., Clark J. H., Orru R. V. A., Maesa B. U. W. Thiosulfonates as Emerging Reactants: Synthesis and Applications. Adv. Synth. Catal. 2020, 362, 3–64 DOI: 10.1002/adsc.201900864 | |
dc.relation.references | 18. Lubenets V. I., Stadnitskaya N. E., Novikov V. P. (2000). Synthesis of thiosulfonates belonging to quinoline derivatives. Russian Journal of Organic Chemistry, 36(6), 851–853. | |
dc.relation.references | 19. Lubenets V., Stadnytska N., Baranovych D., Vasylyuk S., Karpenko O., Havryliakand V., Novikov V. (March 15th 2019). Thiosulfonates: The ProspectiveSubstances against Fungal Infections. In: Fungal Infection. Eds. Érico Silva de Loreto and JulianaSimoni Moraes Tondolo, IntechOpen, London. DOI:10.5772/intechopen.84436. | |
dc.relation.references | 20. Lubenets V., Vasylyuk S., Monka N., Bolibrukh K., Komarovska-Porokhnyavets O., Baranovych D., Musyanovych R., Zaczynska E., Czarny A., Nawrot U., Novikov V. (2017). Synthesis and antimicrobial properties of 4- acylaminobenzenethiosulfoacid S-esters. Saudi Pharmaceutical Journal, 25(2), 266–274. http://dx.doi.org/10.1016/j.jsps.2016.06.007 | |
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dc.relation.references | 24. Lagunin A., Stepanchikova A., Filimonov D., Poroikov V. (2000). PASS: prediction of activity spectra for biological lyactive substances. Bioinformatics. 16 (8),747–748. | |
dc.relation.referencesen | 1. Pietro O. D., Vicente-García E., Taylor M. C., Berenguer D., Viayna E., Lanzoni A., Sola I., Sayago H., Riera C., Fisa R., Clos M. V., Pérez B., Kelly J. M., Lavilla R., Muñoz-Torrero D. (2015) Multicomponent reaction-based synthesis and biological evaluation of tricyclic heterofusedquinolines with multi-trypanosomatid activity. European Journal of Medicinal Chemistry. 105, 120–137. | |
dc.relation.referencesen | 2. Juan Carlos Coa, Wilson Castrillón, Wilson Cardona, Miguel Carda, Victoria Ospina, July Andrea Muñoz, Iván D. Vélez, Sara M. Robledo. (2015) Synthesis, leishmanicidal, trypanocidal and cytotoxic activity of quinoline-hydrazone hybrids. European Journal of Medicinal Chemistry, 101, 746–753. | |
dc.relation.referencesen | 3. Abdel-Wahab B. F., Khidre R. E. and Farahat A. A. (2011). Pyrazole-3(4)-carbaldehyde: synthesis, reactions and biological activity. Arkivoc, 1,. 196–245. | |
dc.relation.referencesen | 4. Mel’nikov N. N. (1987). Pestitsidi.Khimiya, tekhnologiya i primeneniye, Mel’nikov N.N. Moskva: Khimiya, 712. | |
dc.relation.referencesen | 5. Mashkovs’kiy M. D. (2001). Lekarstvennyye sredstva: V 2t T. 2, 14-ye izd., pererab., isp. i dop.-M., OOO "Izdatel’stvo Novaya Volna": Izdatel’ S.B. Davidov, 2. 286. | |
dc.relation.referencesen | 6. Cziaky Z., Korodi F., Frank L and Czink I. (1996). Synthesis and antimycotic activity of new 2-chloro-3-(2- nitro)ethyl- and (2-nitro)vlnylquinolines. Heterocyclic Communications, 2(1), 63–70. | |
dc.relation.referencesen | 7. Delgado J. N., Remers W. A. Wilson and Gisvold’s (1998). Text Book of Organic Medicinal and Pharmaceutical Chemistry, 10 th ed. Lippincott Williams & Wilkins. Text Book, 235–252. | |
dc.relation.referencesen | 8. Farghally A. M., Habib N. S., Hazzaa A. A. B. and El-Sayed O. A. (1985). Synthesis of substituted quinoline-3-carbaldehyde (2,3-dihydrothiazol-2-ylidene) hydrazones of potential antimicrobial activity. Journal de Pharmacie de Belgique, 40(6), 366–372. | |
dc.relation.referencesen | 9. Fournet A., Barrios A. A., Munoz V., Hocquemiller R., Cave A., Richomme P., Bruneton J. (1993). 2-Substituted quinoline alkaloids as potential antileishmanial drugs. Antimicrob Agents Chemother, 37, 859. | |
dc.relation.referencesen | 10. Bekhit A. A., El-Sayed O. A., Aboulmagd E., Park J. Y. (2004). Tetrazolo[1,5-a]quinoline as a potential promising new scaffold for the synthesis of novel anti-infl ammatory and antibacterial agents. Eur. J. Med. Chem, 39(3), 249–255. | |
dc.relation.referencesen | 11. Gupta R., Gupta A. K., Paul S. and Kachroo P. L. (1998). Synthesis and biological activities of some 2- chloro-6/8-substituted-3-(3-alkyl/aryl-5,6-dihydro-s-triazolo [3,4-b][1,3,4]thiadiazol-6-yl)quinolines. Indian Journal Of Chemistry B., 37, 1211–1213. | |
dc.relation.referencesen | 12. Nicolaou K. C., Gross J. L., Kerr M. A. (1996). Synthesis of novel heterocycles related to the Dynemicin A ring skeleton. J. Heterocycl. Chem. 33(3), 735–746. | |
dc.relation.referencesen | 13. Bringmann G., Reichert Y., Kane V. (2004). The total synthesis of streptonigrin and related antitumor antibiotic natural products. Tetrahedron. 60, 3539–3574. | |
dc.relation.referencesen | 14. Davis H. L., Von Hoff D. D., Henney J. T., Rozencweig M. (1978). The role of antitumor antibiotics in current oncologic practice. Cancer Chemother. Pharmacol. 1(2), 83–90. | |
dc.relation.referencesen | 15. Kuz’menko L., Avdeenko A., Konovalova S., Vasylyuk S., Fedorova O., Monka N., Krychkovska A., Lubenets V. (2019). Synthesis and study of pesticidal activity of some N-arylthio-1,4-benzoquinone imines. Biointerface Research in Applied Chemistry. 9(5), 4232 –4238. | |
dc.relation.referencesen | 16. Mandal B., Basu B., RSC Adv. 2014, 4, 13854–13881; D. Witt, Synthesis 2008, 2491–2509; b) J. Yuan, C. Liu, A. Lei, Org. Chem. Front. 2015, 2, 677–680. | |
dc.relation.referencesen | 17.Mampuys P.,McElroy C. R., Clark J. H., Orru R. V. A., Maesa B. U. W. Thiosulfonates as Emerging Reactants: Synthesis and Applications. Adv. Synth. Catal. 2020, 362, 3–64 DOI: 10.1002/adsc.201900864 | |
dc.relation.referencesen | 18. Lubenets V. I., Stadnitskaya N. E., Novikov V. P. (2000). Synthesis of thiosulfonates belonging to quinoline derivatives. Russian Journal of Organic Chemistry, 36(6), 851–853. | |
dc.relation.referencesen | 19. Lubenets V., Stadnytska N., Baranovych D., Vasylyuk S., Karpenko O., Havryliakand V., Novikov V. (March 15th 2019). Thiosulfonates: The ProspectiveSubstances against Fungal Infections. In: Fungal Infection. Eds. Érico Silva de Loreto and JulianaSimoni Moraes Tondolo, IntechOpen, London. DOI:10.5772/intechopen.84436. | |
dc.relation.referencesen | 20. Lubenets V., Vasylyuk S., Monka N., Bolibrukh K., Komarovska-Porokhnyavets O., Baranovych D., Musyanovych R., Zaczynska E., Czarny A., Nawrot U., Novikov V. (2017). Synthesis and antimicrobial properties of 4- acylaminobenzenethiosulfoacid S-esters. Saudi Pharmaceutical Journal, 25(2), 266–274. http://dx.doi.org/10.1016/j.jsps.2016.06.007 | |
dc.relation.referencesen | 21. Lubenets V. I., Stadnytskaia N. E., Novikov V. P. (2000). Syntez tyosulfonatov – proyzvodnykh khynolyna. Zhurn. orh. Khym, 36(6), 883–885. | |
dc.relation.referencesen | 22. Stadnytska N. Ye., Lubenets V. I., Novikov V. P., Komarovska O. Z., Vovk N. I., Kryvoruchko O. M. (2000). Syntez ta biolohichna aktyvnist S-alkil(-8-khinolin)tiosulfonativ. Zhurn. fiziolohichno aktyvnykh rechovyn, 2(30), 27–30. | |
dc.relation.referencesen | 23. Hloriozova T. A., Filimonov D. A., Lahu- nin A. A., Poroikov V. V. (1998). Testirovanie kompiu- ternoi sistemy dlia predskazaniia biolohicheskoi aktivnosti PASS na vyborke novykh khimicheskikh soedinenii. Khim.-farm. zhurnal. 32(12), 32–39. | |
dc.relation.referencesen | 24. Lagunin A., Stepanchikova A., Filimonov D., Poroikov V. (2000). PASS: prediction of activity spectra for biological lyactive substances. Bioinformatics. 16 (8),747–748. | |
dc.relation.uri | http://dx.doi.org/10.1016/j.jsps.2016.06.007 | |
dc.rights.holder | © Національний університет “Львівська політехніка”, 2020 | |
dc.subject | хінолін | |
dc.subject | естери тіосульфокислот | |
dc.subject | прогнозована активність | |
dc.subject | цитатоксичніть | |
dc.subject | токсичність | |
dc.subject | quinoline | |
dc.subject | thiosulfonic acid esters | |
dc.subject | predictive activity | |
dc.subject | cytotoxicity | |
dc.subject | toxicity | |
dc.title | Прогнозований скринінг біологічної активності S-алкілових естерів 8-хінолінтіосульфокислоти | |
dc.title.alternative | Predictive screening of the biological activity of S-alkyl esters of 8-quinolinsulfonic acid | |
dc.type | Article |
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