Zobrazeno 1 - 10
of 14
pro vyhledávání: '"D. Ya. Havrylyuk,"'
Autor:
Kh. V. Malysheva, N. S. Finiuk, O. K. Pavlenko, D. Ya. Havrylyuk,, R. B. Lesyk, R. S. Stoika, O. G. Korchynskyi
Publikováno v:
The Ukrainian Biochemical Journal, Vol 89, Iss SI01, Pp 111-122 (2017)
Rheumatoid arthritis (RA) is an autoimmune inflammatory disease of yet unknown etiology. Tumor necrosis factor α (TNFα) is recognized as a regulatory substance that plays a central role in RA development and progression. On the other side, the bone
Externí odkaz:
https://doaj.org/article/cb4e3b20ae71473b973cecfb8449c47e
Autor:
L. I. Kоbylinska, D. Ya. Havrylyuk, А. О. Ryabtseva, N. E. Mitina, О. S. Zаichenko, R. B. Lesyk, B. S. Zіmenkovsky, R. S. Stoika
Publikováno v:
The Ukrainian Biochemical Journal, Vol 87, Iss 2, Pp 122-132 (2015)
The aim of this study was to compare the effect of new synthetic 4-tiazolidinone derivatives (compounds 3882, 3288 and 3833) and doxorubicin (positive control) in free form and in their complexes with synthetic polyethyleneglycol-containing nanoscale
Externí odkaz:
https://doaj.org/article/535dc5db2a9149439e6172359ecad216
Autor:
N. M. Boiko, O. Yu. Klyuchivska, L. I. Коbylinska, D. Ya. Havrylyuk, A. O. Ryabtseva, N. Ye. Mitina, R. B. Lesyk, O. S. Zаichenko, R. S. Stoika
Publikováno v:
Biotechnologia Acta, Vol 8, Iss 1, Pp 39-48 (2015)
A nanoscale polymeric carrier was used for delivery of novel anticancer compounds – 4-tiazolidinone derivatives – to tumor cells of different lines. It was found that such way of delivery of the above mentioned compounds to target cells significa
Externí odkaz:
https://doaj.org/article/b26f9f4f109348758735d23cf6e44049
Autor:
V. V. Chumak, R. R. Panchuk, N. O. Manko, D. Ya. Havrylyuk, R. V. Lesyk, L. I. Kobylinska, B. S. Zimenkovsky, R. S. Stoika
Publikováno v:
Біологічні студії, Vol 8, Iss 2, Pp 29-42 (2014)
Compounds on the basis of 4-thiazolidinone and its isatin-containing derivatives are characterized by a broad spectrum of biological activities and are potential antineoplastic agents. We have shown that the combination of 4-thiazolidinone and isatin
Externí odkaz:
https://doaj.org/article/6b94ba341ffa4a289115694e01d4b178
Autor:
N. S. Finiuk, O. G. Korchynsky, O. K. Pavlenko, Kh. V. Malysheva, Rostyslav Stoika, Roman Lesyk, D. Ya. Havrylyuk
Publikováno v:
Ukrainian Biochemical Journal, Vol 89, Iss SI01, Pp 111-122 (2017)
Rheumatoid arthritis (RA) is an autoimmune inflammatory disease of yet unknown etiology. Tumor necrosis factor α (TNFα) is recognized as a regulatory substance that plays a central role in RA development and progression. On the other side, the bone
Autor:
Nataliya Mitina, L I Kоbyli nska, Alexander Zaichenko, B S Zіme nkovsky, Rostyslav Stoika, D. Ya. Havrylyuk, Roman Lesyk
Publikováno v:
Ukrainian Biochemical Journal, Vol 88, Iss 1, Pp 51-60 (2016)
The aim of this study was to compare the effect of new synthetic 4-thiazolidinone derivatives (potential anticancer compounds denoted as 3882, 3288 and 3833) and doxorubicin (positive control) in free form and in their complexes with synthetic polyet
Autor:
D. Ya. Havrylyuk
Publikováno v:
Journal of Organic and Pharmaceutical Chemistry. 12:59-64
The application of the [2+3]-cyclocondensation reaction for the synthesis of 2-pyrazoline substituted thiazolidinones, as well as bioisosteric pyrazoline-thiazoles has been analyzed. Following the literature data 4,5-dihydro- 1-carbothioamides are us
Autor:
Lesya Kobylinska, Rostyslav Stoika, Roman Lesyk, R. R. Panchuk, Borys Zimenkovsky, N. O. Manko, D. Ya. Havrylyuk, V. V. Chumak
Publikováno v:
Біологічні студії, Vol 8, Iss 2, Pp 29-42 (2014)
Compounds on the basis of 4-thiazolidinone and its isatin-containing derivatives are characterized by a broad spectrum of biological activities and are potential antineoplastic agents. We have shown that the combination of 4-thiazolidinone and isatin
Autor:
Borys Zimenkovsky, D. Ya. Havrylyuk, V. V. Chumak, Roman Lesyk, R. R. Panchuk, M. R. Fil, Rostyslav Stoika
Publikováno v:
Biopolymers and Cell, Vol 28, Iss 2, Pp 121-128 (2012)
Цель. Исследовать механизмы индукции апоптических сигнальных путей новыми гетероциклическими производными 4-тиазолидонов со структур
Publikováno v:
Scopus-Elsevier
Biopolymers and Cell, Vol 27, Iss 2, Pp 147-153 (2011)
Biopolymers and Cell, Vol 27, Iss 2, Pp 147-153 (2011)
Aim was to compare the action of 2A5DHT compound (dual COX-2/5-LOX inhibitor) and conventional non-steroidal anti-inflammatory drugs towards parameters of nitric oxide (NO) system and intensity of oxidative stress in the mucous membrane of the large
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ef0dd48aa4f7c27af0e2f82d1fd4f620
http://www.scopus.com/inward/record.url?eid=2-s2.0-79957764684&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-79957764684&partnerID=MN8TOARS