Synthesis of thiosulphonate and amino acid derivatives of benzochinone and predicted screening of their biological activity
dc.citation.epage | 46 | |
dc.citation.issue | 2 | |
dc.citation.spage | 40 | |
dc.contributor.affiliation | Національний університет “Львівська політехніка” | |
dc.contributor.affiliation | Lviv Polytechnic National University | |
dc.contributor.author | Монька, Н. Я. | |
dc.contributor.author | Журахівська, Л. Р. | |
dc.contributor.author | Курка, М. С. | |
dc.contributor.author | Шиян, Г. Б. | |
dc.contributor.author | Семенчук, Ю. М. | |
dc.contributor.author | Лубенець, В. І. | |
dc.contributor.author | Monka, N. Ya. | |
dc.contributor.author | Zhurakhivska, L. R. | |
dc.contributor.author | Kurka, M. S. | |
dc.contributor.author | Shyian, H. B. | |
dc.contributor.author | Semenchuk, Yu. M. | |
dc.contributor.author | Lubenets, V. I. | |
dc.coverage.placename | Lviv | |
dc.coverage.placename | Lviv | |
dc.date.accessioned | 2024-01-22T08:47:19Z | |
dc.date.available | 2024-01-22T08:47:19Z | |
dc.date.created | 2020-03-16 | |
dc.date.issued | 2020-03-16 | |
dc.description.abstract | Похідні хіноїдного ряду приваблюють, не лише як цікаві синтони для синтезу, а також як потенційні біологічно активні речовини, тому актуальним є модифікація сполук хінонового ряду різними фармакоформними фрагментами. Проведено структурний дизайн хлор- та броманілу дисульфуровмісними фрагментами, а саме тіосульфонатними, та хлоранілу – фрагментом 4- амінобутанової кислоти. Розроблено методики синтезу та досліджено фізико-хімічні характеристики тіосульфонатних та амінокислотних похідних: 2,5-біс(тіосульфонатних)-3,6-галоген-1,4-бензохінонів та 2,5-біс(3-карбоксипропіламіно)-3,6-дихлорбензохінону. Перспективність дизайну хлор- та броманілу тіосульфонатними фрагментами та хлоранілу фрагментом 4-амінобутанової кислоти підтверджена результатами прогнозування біологічної активності 5 а, b, 6 а, b, 7 з використанням онлайн-ресурсу PASS Online. Зокрема субстанція 5b, яку одержали, є перспективною для досліджень на Antiviral (Picornavirus). Одержані результати прогнозованого скринінгу цитотоксичності свідчать про доцільність проведення експериментальних досліджень методами in vitro на протиракові активності стосовно лінії ракових клітин гематопоїдної і лімфоїдної тканини, легень, шкіри, яєчників, крові, молочної залози, нирок, товстої кишки, головного мозку. | |
dc.description.abstract | Quinoid derivatives are attractive not only as interesting synthons for synthesis, but also as potential biologically active substances, so it is important to modify the compounds of the quinone series with different pharmacoform fragments. In this work, the structural design of chlorine and bromanyl disulfur-containing fragments, namely thiosulfonate, and chloranyl – a fragment of 4-aminobutanoic acid. Methods of synthesis were developed and physicochemical characteristics of thiosulfonate and amino acid derivatives were studied: 2,5-bis (thiosulfonate) -3,6-halogen -1,4-benzoquinones and 2,5-bis (3-carboxypropylamino) -3,6 – dichlorobenzoquinone. The prospects for the design of chlorine and bromanyl thiosulfonate fragments and chloranyl fragment of 4-aminobutanoic acid are confirmed by the results of predicting the biological activity of 5 a, b, 6 a, b, 7 using the online resource PASS Online. In particular, the substance 6a obtained by us is promising in terms of research on Antiviral (Picornavirus). The obtained results of predicted cytotoxicity screening indicate the feasibility of conducting experimental studies by in vitro methods on anticancer activity against cancer cell lines of hematopoietic and lymphoid tissue, lungs, skin, ovaries, blood, breast, kidney, colon, brain. | |
dc.format.extent | 40-46 | |
dc.format.pages | 7 | |
dc.identifier.citation | Synthesis of thiosulphonate and amino acid derivatives of benzochinone and predicted screening of their biological activity / N. Ya. Monka, L. R. Zhurakhivska, M. S. Kurka, H. B. Shyian, Yu. M. Semenchuk, V. I. Lubenets // Chemistry, Technology and Application of Substances. — Lviv : Lviv Politechnic Publishing House, 2021. — Vol 4. — No 2. — P. 40–46. | |
dc.identifier.citationen | Synthesis of thiosulphonate and amino acid derivatives of benzochinone and predicted screening of their biological activity / N. Ya. Monka, L. R. Zhurakhivska, M. S. Kurka, H. B. Shyian, Yu. M. Semenchuk, V. I. Lubenets // Chemistry, Technology and Application of Substances. — Lviv : Lviv Politechnic Publishing House, 2021. — Vol 4. — No 2. — P. 40–46. | |
dc.identifier.doi | doi.org/10.23939/ctas2021.02.040 | |
dc.identifier.uri | https://ena.lpnu.ua/handle/ntb/60906 | |
dc.language.iso | en | |
dc.publisher | Lviv Politechnic Publishing House | |
dc.relation.ispartof | Chemistry, Technology and Application of Substances, 2 (4), 2021 | |
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dc.relation.references | 3. Rani M. E. (2014). Spectrophotometric determination of cefadroxil with 2,3 – dichloro-5,6 dicyano-1, 4-benzoquinone. World Journal of Pharmaceutical Research. Vol. 3. Issue 9. Р. 1196-1200 | |
dc.relation.references | 4. Sheikh R., Amin A., Gouda A., Zahran D. (2017). Validated spectrophotometric methods for determination of cefdinir in pure and dosage forms through charge transfer complexation using alizarin derivatives. International Journal of Research in Pharmacy and Pharmaceutical Sciences. Vol. 2. Issue 6. Р. 11-18 | |
dc.relation.references | 5. Ali Ahmed S., Elbashir A., Aboul-Enein H. (2015). New spectrophotometric method for determination of cephalosporins in pharmaceutical formulations. Arabian Journal Of Chemistry. Vol. 8. Issue 2. P. 233-239. doi: 10.1016/j.arabjc.2011.08.012 | |
dc.relation.references | 6. Kumari N. A., Vasundhara A. (2016). A noval method development for spectrophotometric determination of ertapenem in bulk and injection formulations by NQS. International Journal of Science Technology and Management. Vol. 5. Is. 1. P. 1–9. | |
dc.relation.references | 7. Omar M., Hammad M., Eltoukhi W. (2017). Spectrophotometric Determination of Certain Antimigraine Drugs in Pharmaceutical Formulations Using p-Chloranil Reagent; Application to Content Uniformity Testing. Analytical Chemistry Letters. Vol. 7. Issue 5. P. 611–622. | |
dc.relation.references | 8. Sotirova A, Avramova T, Stoitsova S, Lazarkevich I, Lubenets V, Karpenko E, Galabova D. (2012). The importance of rhamnolipid-biosurfactantinduced changes in bacterial membrane lipids of Bacillus subtilis for the antimicrobial activity of thiosulfonates. Curr. Microbiol. № 65(5): 534–541 | |
dc.relation.references | 9. E. Mochizuki, H. Nakazawa. (1995). Sulfur Components of Garlic and Garlic Preparations and their Biological Activities. Foods & Food Ingredients Journal of Japan. No. 164. P. 36–45. | |
dc.relation.references | 10. M. J. Peinado, R. Ruiz, A. Echavarri, and L. A. Rubio. (2012). Garlic derivative propyl propane thiosulfonate is effective against broiler enteropathogens in vivo. Poultry Science. Vol. 91. Р. 2148–2157 | |
dc.relation.references | 11. A. Mital, V. S. Negi and U. Ramachandran. (2008). Synthesis and Biological Evaluation of Naphthalene-1,4-dione Derivatives as Potent Antimycobacterial Agents. Medicinal Chemistry. № 4, 492–497. | |
dc.relation.references | 12. V. Dziuba, O. Kuchmenko. (2017). Suchasni uiavlennia pro rol ubikhinonu v protsesakh metabolizmu klityny. Visnyk Lvivskoho universytetu. Seriia biolohichna. V. 75. С. 3–13 [Ukraine] | |
dc.relation.references | 13. Kolesnikov V. T. Vid L. V. Kuzmenko L. O. (1982). 1-benzenesulfonylsulfany-l-4 nitrobenzene Hurnal organicheskoy khimii 18.2163. (in Russian). | |
dc.relation.references | 14. L. Kuz'menko, A. Avdeenko, S. Konovalova, S. Vasylyuk, O. Fedorova, N. Monka, A. Krychkovska,V. Lubenets. (2019). Synthesis and study of pesticidal activity of some N-arylthio-1,4-benzoquinone imines. Biointerface Research in Applied Chemistry. Vol. 9, Is. 5, 4232–4238. https://doi.org/10.33263/BRIAC95.232238 | |
dc.relation.references | 15. Vasylyuk, S.; Komarovska-Porokhnyavets, O.; Novikov, V.; Lubenets, V. (2018). Modification of Alkyl Esters of 4- Aminobenzenethiosulfonic Acid by s-Triazine Fragment and Investigation of their Growth-Regulative Activity. Chemistry and Chemical Technology 12, 24, https://doi.org/10.23939/chcht12.01.024. | |
dc.relation.references | 16. 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, 266, https://doi.org/10.1016/j.jsps.2016.06.007. | |
dc.relation.references | 17. Núñez L. C., Arjona A.B., A.E. Guillamón, López A. V., Ma (2018). Concepción Navarro Moll, Ana Sanz Rus Use of propyl propane thiosulfinate and propyl propane thiosulfonate for the prevention and reduction of parasites in aquatic animals Patent No.: US 2018/0014538 А1, Date of Patent: Jan. 18, | |
dc.relation.references | 18. Santos dos, Edson dos A. Goncalves F. Prado P. C. Sasaki D. Y. Lima D.P.; M. L. (2012). Rodrigues Synthesis method for thiosulfonate and report of its insecticidal activity in Anagasta kuehniella (Lepidoptera: Pyralidae) International Journal of Molecular Sciences. 13, 15241 | |
dc.relation.references | 19. Lubenets V. I., Havryliak V. V., Pylypets A. Z., Nakonechna A. V. (2018). Changes in the spectrum of proteins and phospholipids in tissues of rats exposed to thiosulfanilates. Regulatory mechanisms in biosystems 9,4,52 | |
dc.relation.references | 20. Pylypets A. Z., Iskra R. Ya, Havryliak V. V, Nakonechna A. V, Novikov V. P, Lubenets V. I. (2017). Effects of thiosulfonates on the lipid composition of rat tissues. Ukr. Biochem J. 89,6,56. | |
dc.relation.references | 21. T. A. Gloriozova, D. A. Filimonov, A. A. Lagunin, V. V. Poroykov (1998) Testirovaniye komp'yuternoy sistemy dlya predskazaniya biologicheskoy aktivnosti PASS na vyborke novykh khimicheskikh soyedineniy. Khim.-farm. zhurnal. 32(12), 32–39. [in Russian] | |
dc.relation.references | 22. A. Lagunin, A. Stepanchikova, D. Filimonov, V. Poroikov (2000). PASS: prediction of activity spectra for biologically active substances. Bioinformatics. 16 (8), 747–748. | |
dc.relation.references | 23. Lagunin A. A., Dubovskaja V. I., Rudik A. V., Pogodin P. V., Druzhilovskiy D. S., Gloriozova T. A., Filimonov D. A., Sastry G. N., Poroikov V. V. (2018). CLC-Pred: a freely available web-service for in silico prediction of human cell line cytotoxicity for drug-like compounds. PLOS One, 13 (1), e0191838. DOI: 10.1371/journal.pone.0191838 | |
dc.relation.references | 24. Pylypets A. Z., Iskra R. Y., Havryliak V. V., Nakonechna A. V., Novikov V. P. Lubenets, V., (2017). Effects of thiosulfonates on the lipid composition of rat tissues. Ukr. Biochem. J., Vol. 89, № 6, 56–62 doi: https://doi.org/10.15407/ubj89.06.056 | |
dc.relation.references | 25. Oriabinska L. B., Starovoitova S. О., Vasylyuk S. V., Novikov V. P. (2017). Ethylthiosulfanilate effect on Candida tropicalis. Ukr. Biochem. J., Vol. 89, № 5 70–76 doi: https://doi.org/10.15407/ubj89.05.070 | |
dc.relation.referencesen | 1. K. P. Medvedeva, A. O. Donchenko, S. O. Vasyuk. (2019). Zastosuvannya pohidnih hinonu dlya spektrofotometrichnogo viznachennya likars'kih zasobiv. Aktual'ni pitannya farmacevtichnoi i medichnoi nauki ta praktiki. V. 12, No3(31), 250–255 DOI: 10.14739/2409-2932.2019.3.184173 [Ukraine] | |
dc.relation.referencesen | 2. Donchenko A. O., Vasyuk S. O., Portna K. P. (2015). Vikoristannya 2,3-dihlor-1,4-naftohinonu dlya spektrofotometrichnogo viznachennya acetilcisteinu v likars'kih preparatah. Aktual'ni pitannya farmacevtichnoi i medichnoi nauki ta praktiki. No 1. P. 36-39. https://doi.org/10.14739/2409-2932.2015.1.41374 [Ukraine] | |
dc.relation.referencesen | 3. Rani M. E. (2014). Spectrophotometric determination of cefadroxil with 2,3 – dichloro-5,6 dicyano-1, 4-benzoquinone. World Journal of Pharmaceutical Research. Vol. 3. Issue 9. R. 1196-1200 | |
dc.relation.referencesen | 4. Sheikh R., Amin A., Gouda A., Zahran D. (2017). Validated spectrophotometric methods for determination of cefdinir in pure and dosage forms through charge transfer complexation using alizarin derivatives. International Journal of Research in Pharmacy and Pharmaceutical Sciences. Vol. 2. Issue 6. R. 11-18 | |
dc.relation.referencesen | 5. Ali Ahmed S., Elbashir A., Aboul-Enein H. (2015). New spectrophotometric method for determination of cephalosporins in pharmaceutical formulations. Arabian Journal Of Chemistry. Vol. 8. Issue 2. P. 233-239. doi: 10.1016/j.arabjc.2011.08.012 | |
dc.relation.referencesen | 6. Kumari N. A., Vasundhara A. (2016). A noval method development for spectrophotometric determination of ertapenem in bulk and injection formulations by NQS. International Journal of Science Technology and Management. Vol. 5. Is. 1. P. 1–9. | |
dc.relation.referencesen | 7. Omar M., Hammad M., Eltoukhi W. (2017). Spectrophotometric Determination of Certain Antimigraine Drugs in Pharmaceutical Formulations Using p-Chloranil Reagent; Application to Content Uniformity Testing. Analytical Chemistry Letters. Vol. 7. Issue 5. P. 611–622. | |
dc.relation.referencesen | 8. Sotirova A, Avramova T, Stoitsova S, Lazarkevich I, Lubenets V, Karpenko E, Galabova D. (2012). The importance of rhamnolipid-biosurfactantinduced changes in bacterial membrane lipids of Bacillus subtilis for the antimicrobial activity of thiosulfonates. Curr. Microbiol. No 65(5): 534–541 | |
dc.relation.referencesen | 9. E. Mochizuki, H. Nakazawa. (1995). Sulfur Components of Garlic and Garlic Preparations and their Biological Activities. Foods & Food Ingredients Journal of Japan. No. 164. P. 36–45. | |
dc.relation.referencesen | 10. M. J. Peinado, R. Ruiz, A. Echavarri, and L. A. Rubio. (2012). Garlic derivative propyl propane thiosulfonate is effective against broiler enteropathogens in vivo. Poultry Science. Vol. 91. R. 2148–2157 | |
dc.relation.referencesen | 11. A. Mital, V. S. Negi and U. Ramachandran. (2008). Synthesis and Biological Evaluation of Naphthalene-1,4-dione Derivatives as Potent Antimycobacterial Agents. Medicinal Chemistry. No 4, 492–497. | |
dc.relation.referencesen | 12. V. Dziuba, O. Kuchmenko. (2017). Suchasni uiavlennia pro rol ubikhinonu v protsesakh metabolizmu klityny. Visnyk Lvivskoho universytetu. Seriia biolohichna. V. 75. P. 3–13 [Ukraine] | |
dc.relation.referencesen | 13. Kolesnikov V. T. Vid L. V. Kuzmenko L. O. (1982). 1-benzenesulfonylsulfany-l-4 nitrobenzene Hurnal organicheskoy khimii 18.2163. (in Russian). | |
dc.relation.referencesen | 14. L. Kuz'menko, A. Avdeenko, S. Konovalova, S. Vasylyuk, O. Fedorova, N. Monka, A. Krychkovska,V. Lubenets. (2019). Synthesis and study of pesticidal activity of some N-arylthio-1,4-benzoquinone imines. Biointerface Research in Applied Chemistry. Vol. 9, Is. 5, 4232–4238. https://doi.org/10.33263/BRIAC95.232238 | |
dc.relation.referencesen | 15. Vasylyuk, S.; Komarovska-Porokhnyavets, O.; Novikov, V.; Lubenets, V. (2018). Modification of Alkyl Esters of 4- Aminobenzenethiosulfonic Acid by s-Triazine Fragment and Investigation of their Growth-Regulative Activity. Chemistry and Chemical Technology 12, 24, https://doi.org/10.23939/chcht12.01.024. | |
dc.relation.referencesen | 16. 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, 266, https://doi.org/10.1016/j.jsps.2016.06.007. | |
dc.relation.referencesen | 17. Núñez L. C., Arjona A.B., A.E. Guillamón, López A. V., Ma (2018). Concepción Navarro Moll, Ana Sanz Rus Use of propyl propane thiosulfinate and propyl propane thiosulfonate for the prevention and reduction of parasites in aquatic animals Patent No., US 2018/0014538 A1, Date of Patent: Jan. 18, | |
dc.relation.referencesen | 18. Santos dos, Edson dos A. Goncalves F. Prado P. C. Sasaki D. Y. Lima D.P.; M. L. (2012). Rodrigues Synthesis method for thiosulfonate and report of its insecticidal activity in Anagasta kuehniella (Lepidoptera: Pyralidae) International Journal of Molecular Sciences. 13, 15241 | |
dc.relation.referencesen | 19. Lubenets V. I., Havryliak V. V., Pylypets A. Z., Nakonechna A. V. (2018). Changes in the spectrum of proteins and phospholipids in tissues of rats exposed to thiosulfanilates. Regulatory mechanisms in biosystems 9,4,52 | |
dc.relation.referencesen | 20. Pylypets A. Z., Iskra R. Ya, Havryliak V. V, Nakonechna A. V, Novikov V. P, Lubenets V. I. (2017). Effects of thiosulfonates on the lipid composition of rat tissues. Ukr. Biochem J. 89,6,56. | |
dc.relation.referencesen | 21. T. A. Gloriozova, D. A. Filimonov, A. A. Lagunin, V. V. Poroykov (1998) Testirovaniye komp'yuternoy sistemy dlya predskazaniya biologicheskoy aktivnosti PASS na vyborke novykh khimicheskikh soyedineniy. Khim.-farm. zhurnal. 32(12), 32–39. [in Russian] | |
dc.relation.referencesen | 22. A. Lagunin, A. Stepanchikova, D. Filimonov, V. Poroikov (2000). PASS: prediction of activity spectra for biologically active substances. Bioinformatics. 16 (8), 747–748. | |
dc.relation.referencesen | 23. Lagunin A. A., Dubovskaja V. I., Rudik A. V., Pogodin P. V., Druzhilovskiy D. S., Gloriozova T. A., Filimonov D. A., Sastry G. N., Poroikov V. V. (2018). CLC-Pred: a freely available web-service for in silico prediction of human cell line cytotoxicity for drug-like compounds. PLOS One, 13 (1), e0191838. DOI: 10.1371/journal.pone.0191838 | |
dc.relation.referencesen | 24. Pylypets A. Z., Iskra R. Y., Havryliak V. V., Nakonechna A. V., Novikov V. P. Lubenets, V., (2017). Effects of thiosulfonates on the lipid composition of rat tissues. Ukr. Biochem. J., Vol. 89, No 6, 56–62 doi: https://doi.org/10.15407/ubj89.06.056 | |
dc.relation.referencesen | 25. Oriabinska L. B., Starovoitova S. O., Vasylyuk S. V., Novikov V. P. (2017). Ethylthiosulfanilate effect on Candida tropicalis. Ukr. Biochem. J., Vol. 89, No 5 70–76 doi: https://doi.org/10.15407/ubj89.05.070 | |
dc.relation.uri | https://doi.org/10.14739/2409-2932.2015.1.41374 | |
dc.relation.uri | https://doi.org/10.33263/BRIAC95.232238 | |
dc.relation.uri | https://doi.org/10.23939/chcht12.01.024 | |
dc.relation.uri | https://doi.org/10.1016/j.jsps.2016.06.007 | |
dc.relation.uri | https://doi.org/10.15407/ubj89.06.056 | |
dc.relation.uri | https://doi.org/10.15407/ubj89.05.070 | |
dc.rights.holder | © Національний університет “Львівська політехніка”, 2021 | |
dc.subject | бензохінон | |
dc.subject | хлораніл | |
dc.subject | броманіл | |
dc.subject | тіосульфонат | |
dc.subject | прогнозована активність | |
dc.subject | цитотоксичніть | |
dc.subject | benzoquinone | |
dc.subject | chloranyl | |
dc.subject | bromanyl | |
dc.subject | thiosulfonate | |
dc.subject | predicted activity | |
dc.subject | cytotoxicity | |
dc.title | Synthesis of thiosulphonate and amino acid derivatives of benzochinone and predicted screening of their biological activity | |
dc.title.alternative | Синтез тіосульфонатних та амінокислотних похідних бензохінону та прогнозований скринінг їх біологічної активності | |
dc.type | Article |
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