Modification of alkyl esters of 4-aminobenzenethiosulfonic acid by S-triazine fragment and investigation of their growth-regulative activity

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dc.citation.epage28
dc.citation.issue1
dc.citation.spage24
dc.citation.volume12
dc.contributor.affiliationLviv National Polytechnic University
dc.contributor.authorVasylyuk, Sofiya
dc.contributor.authorKomarovska-Porokhnyavets, Olena
dc.contributor.authorNovikov, Volodymyr
dc.contributor.authorLubenets, Vira
dc.coverage.placenameLviv
dc.date.accessioned2019-01-29T12:53:43Z
dc.date.available2019-01-29T12:53:43Z
dc.date.created2018-01-20
dc.date.issued2018-01-20
dc.description.abstractДосліджено ацилювання аміногрупи алкі- лових S-естерів 4-амінобензентіосульфокислоти ціанурхло- ридом. Серію естерів із триазиновим фрагментом було синтезовано та охарактеризовано елементарним аналізом, 1H- ЯМР та ІЧ-спектроскопією. Досліджено рістрегулювальну ак- тивність синтезованих сполук. Визначено певний вплив струк- тури тіосульфоестерів на їх рістрегулювальну активність.
dc.description.abstractThe acylation of aminogroup of alkyl S-esters 4-aminobenzenthiosulfoacid with cyanurchloride was investigated. Series of esters with triazine fragment were synthesized and characterized by elemental analysis, 1H NMR and IR spectroscopy. The growth-regulative activity of the synthesized compounds was researched. Some appropriate effect of thiosulfoesters structure upon their growth-regulative activity was determined.
dc.format.extent24-28
dc.format.pages5
dc.identifier.citationModification of alkyl esters of 4-aminobenzenethiosulfonic acid by S-triazine fragment and investigation of their growth-regulative activity / Sofiya Vasylyuk, Olena Komarovska-Porokhnyavets, Volodymyr Novikov, Vira Lubenets // Chemistry & Chemical Technology. — Lviv : Lviv Politechnic Publishing House, 2-18. — Vol 12. — No 1. — P. 24–28.
dc.identifier.citationenModification of alkyl esters of 4-aminobenzenethiosulfonic acid by S-triazine fragment and investigation of their growth-regulative activity / Sofiya Vasylyuk, Olena Komarovska-Porokhnyavets, Volodymyr Novikov, Vira Lubenets // Chemistry & Chemical Technology. — Lviv : Lviv Politechnic Publishing House, 2-18. — Vol 12. — No 1. — P. 24–28.
dc.identifier.urihttps://ena.lpnu.ua/handle/ntb/43928
dc.language.isoen
dc.publisherLviv Politechnic Publishing House
dc.relation.ispartofChemistry & Chemical Technology, 1 (12), 2-18
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dc.relation.referencesen[1]Mykhaylichenko S., Chesnyuk A., Firhanh S. et al., Pat. RU2230063, Publ. July 10, 2004.
dc.relation.referencesen[2] Kvak S., Tretyakova O., Kotlyarov N. et al., Pat. RU 2091375, Publ. Sept. 27, 1997.
dc.relation.referencesen[3]Mel'nikov N., Pestitsidy. Khimiya, Tekhnologiya i Primeneniye. Khimiya, Moskva 1987.
dc.relation.referencesen[4] Saczewski F., Bulakowska A., Bednarski P., Grunert R., Eur. J. Med. Chem., 2006, 41, 219.https://doi.org/10.1016/j.ejmech.2005.10.013
dc.relation.referencesen[5] Polovkovych S., Karkhut A., Marintsova N. et al., J. Heterocyclic Chem., 2013, 50, 1419.https://doi.org/10.1002/jhet.890
dc.relation.referencesen[6] Zhou Y., Sun Z., Froelich J. M., Hermann T., Wall D., Bioorg. Med. Chem. Lett., 2006, 16, 5451.https://doi.org/10.1016/j.bmcl.2006.07.052
dc.relation.referencesen[7] Kelarev V., Koshelev V., Belov N., Khimiya Heterotsiklicheskikh Soyedineniy, 1994, 2, 240.
dc.relation.referencesen[8] Polovkovych S., Karkhut A., Marintsova N., Novikov V., Heteroatom Chem., 2010, 21, 392. https://doi.org/10.1002/hc.20631
dc.relation.referencesen[9] Su J.-Y., Xu X.-H., Zeng L.-M. et al., Phytochemistry, 1998, 48,583. https://doi.org/10.1016/S0031-9422(98)00015-6
dc.relation.referencesen[10] Lubenets V., Vasylyuk S., Baranovych D. et al., Chem. Agric. Environ, 2007, 8, 163.
dc.relation.referencesen[11] Banya A., Karpenko O., Lubenets V. et al., Biotechnologia Acta, 2015, 8, 71. https://doi.org/10.15407/biotech8.05.071
dc.relation.referencesen[12] Baranovych D., Lubenets V., Novikov V., Ukr. Khim. Zh.,1999, 65, 130.
dc.relation.referencesen[13] Baranovych D., Komarovska O., Lubenets V., Novikov V., Physiolohichno Aktyvni Rechovyny, 2000, 2, 33.
dc.relation.referencesen[14] Takada N., Watanabe N., Suenaga K. et al., Tetrahedron Lett.,2001, 42, 6557. https://doi.org/10.1016/S0040-4039(01)01314-4
dc.relation.referencesen[15] Block E., Thiruvazhi M., Toscano P. et al., J. Am. Chem. Soc.,1996, 118, 2790. https://doi.org/10.1021/ja951134t
dc.relation.referencesen[16] Block E., Shu-Hai Z., J. Org. Chem., 1992, 57, 5815.https://doi.org/10.1021/jo00048a007
dc.relation.referencesen[17] Lubenets V., Ukr. Khim. Zh., 2003, 69,109.
dc.relation.referencesen[18] Lubenets V., Vasylyuk S., Monka N. et al., Pat. Ukr. 64412, Publ. Nov. 10, 2011.
dc.relation.referencesen[19] Halenova T., Nikolaeva I., Nakonechna A. et al., Ukr. Biochem. J., 2015, 87, 83.
dc.relation.referencesen[20] Nawrot U., Zaczynska E., Czarny A. et al.:Mikologia Lekarska, 2012, 4, 143.
dc.relation.referencesen[21] Lubenets V., Karpenko O., PonomarenkoM. et al., Chem. Chem. Technol., 2013, 7, 119.
dc.relation.referencesen[22] Shyam Pranab K., Soobin Son, Hye-Young Jang: Eur. J. Org. Chem., 2017, 34, 5025. https://doi.org/10.1002/ejoc.201700971
dc.relation.referencesen[23] SmithM., Hunter R., Stellenboom N. et al., Biochim. Biophys. Acta, 2016, 1860, 1439.https://doi.org/10.1016/j.bbagen.2016.03.032.
dc.relation.referencesen[24] Lubenets V., Vasylyuk S., Baranovych D., Novikov V., Pat. Ukr. 14985, Publ. Jun 15, 2006.
dc.relation.referencesen[25] Sergeyeva T.:Metodika Laboratornykh Ispytaniy Herbitsidov. Zashchita rasteniy, Moskva 1963.
dc.relation.referencesen[26] Bandgar B., Pandit S., J. Sulfur Chem., 2004, 25, 347.https://doi.org/10.1080/17415990412331317946
dc.relation.referencesen[27] Vasylyuk S., Lubenets V., Bychko YU.I., Novykov V.P., Khimiya geterotsiklicheskikh soyedineniy, 2008, 1, 132.
dc.relation.urihttps://doi.org/10.1016/j.ejmech.2005.10.013
dc.relation.urihttps://doi.org/10.1002/jhet.890
dc.relation.urihttps://doi.org/10.1016/j.bmcl.2006.07.052
dc.relation.urihttps://doi.org/10.1002/hc.20631
dc.relation.urihttps://doi.org/10.1016/S0031-9422(98)00015-6
dc.relation.urihttps://doi.org/10.15407/biotech8.05.071
dc.relation.urihttps://doi.org/10.1016/S0040-4039(01)01314-4
dc.relation.urihttps://doi.org/10.1021/ja951134t
dc.relation.urihttps://doi.org/10.1021/jo00048a007
dc.relation.urihttps://doi.org/10.1002/ejoc.201700971
dc.relation.urihttps://doi.org/10.1016/j.bbagen.2016.03.032
dc.relation.urihttps://doi.org/10.1080/17415990412331317946
dc.rights.holder© Національний університет „Львівська політехніка“, 2018
dc.rights.holder© Vasylyuk S., Komarovska-Porokhnyavets O., Novikov V., Lubenets V., 2018
dc.subjectтіосульфокислотні похідні
dc.subjectтіосуль- фоестери
dc.subjects-триазин
dc.subjectрістрегулювальна активність
dc.subjectthiosulfoacid derivatives
dc.subjectthiosulfoesters
dc.subjects-triazine
dc.subjectgrowth-regulative activity
dc.titleModification of alkyl esters of 4-aminobenzenethiosulfonic acid by S-triazine fragment and investigation of their growth-regulative activity
dc.title.alternativeМодифікація алкілових естерів 4-амінобензентіосульфокислоти СИМ-триазиновим фрагментом та дослідження їх рістрегулювальної активності
dc.typeArticle

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Chemistry & Chemical Technology. – 2018. – Vol. 12, No. 1