Anna Kryshchyshyn-Dylevych
Anna Kryshchyshyn-Dylevych
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Thiazolidinone motif in anticancer drug discovery. Experience of DH LNMU medicinal chemistry scientific group
RB Lesyk, BS Zimenkovsky, DV Kaminskyy, AP Kryshchyshyn, ...
Biopolymers and Cell 27 (2), 107-117, 2011
5-Ene-4-thiazolidinones–An efficient tool in medicinal chemistry
D Kaminskyy, A Kryshchyshyn, R Lesyk
European journal of medicinal chemistry 140, 542-594, 2017
A new domino-Knoevenagel–hetero-Diels–Alder reaction
VS Matiychuk, RB Lesyk, MD Obushak, A Gzella, DV Atamanyuk, ...
Tetrahedron Letters 49 (31), 4648-4651, 2008
Recent developments with rhodanine as a scaffold for drug discovery
D Kaminskyy, A Kryshchyshyn, R Lesyk
Expert Opinion on Drug Discovery 12 (12), 1233-1252, 2017
Fused Thiopyrano [2, 3-d] thiazole Derivatives as Potential Anticancer Agents
A Kryshchychyn, D Atamanyuk, R Lesyk
Sci Pharm 80, 509-529, 2012
Trends in research of antitrypanosomal agents among synthetic heterocycles
A Kryshchyshyn, D Kaminskyy, P Grellier, R Lesyk
European journal of medicinal chemistry 85, 51-64, 2014
Isothiocoumarin-3-carboxylic acid derivatives: synthesis, anticancer and antitrypanosomal activity evaluation
D Kaminskyy, A Kryshchyshyn, I Nektegayev, O Vasylenko, P Grellier, ...
European Journal of Medicinal Chemistry 75, 57-66, 2014
Synthesis of 5-enamine-4-thiazolidinone derivatives with trypanocidal and anticancer activity
S Holota, A Kryshchyshyn, H Derkach, Y Trufin, I Demchuk, A Gzella, ...
Bioorganic chemistry 86, 126-136, 2019
Thiazolidinone/thiazole based hybrids–New class of antitrypanosomal agents
A Kryshchyshyn, D Kaminskyy, O Karpenko, A Gzella, P Grellier, R Lesyk
European journal of medicinal chemistry 174, 292-308, 2019
Anticancer potential of 4-azolidones and related heterocycles
R Lesyk, B Zimenkovsky, D Kaminskyy, S Holota, D Atamanyuk, ...
Annal. UMCS. Sectio 1500, 19, 2006
Anticancer properties of 4-thiazolidinone derivatives depend on peroxisome proliferator-activated receptor gamma (PPARγ)
KA Szychowski, ML Leja, DV Kaminskyy, AP Kryshchyshyn, UE Binduga, ...
European Journal of Medicinal Chemistry 141, 162-168, 2017
Investigation of anticancer and anti-parasitic activity of thiopyrano[2,3-d]thiazoles bearing norbornane moiety
LRB Kryshchyshyn A. P., Atamanyuk D. V., Kaminskyy D. V., Grellier Ph.
Biopolym. Cell. 33 (3), 183-205, 2017
Synthesis and anticancer activity in vitro of isothiochromеno [3,4-d] thiazole derivatives
A Kryshchychyn, B Zimenkovsky, R Lesyk
Annales Universitatis Mariae Curie-Sklodowska (Lublin–Polonia) Sectio DDD …, 2008
Thiopyrano [2, 3-d] Thiazoles as New Efficient Scaffolds in Medicinal Chemistry
A Kryshchyshyn, O Roman, A Lozynskyi, R Lesyk
Scientia pharmaceutica 86 (2), 26, 2018
The study of the antityrpanosomal activity of thiazolidinones and related heterocyclic systems (In Ukrainian)
AP Kryshchyshyn, DV Kaminskyy, NI Zelisko, DV Khyluk, F Grellier, L R.B.
Журнал органічної і фармацевтичної хімії/ Journal of organic and …, 2013
Development of Predictive QSAR Models of 4‐Thiazolidinones Antitrypanosomal Activity Using Modern Machine Learning Algorithms
A Kryshchyshyn, O Devinyak, D Kaminskyy, P Grellier, R Lesyk
Molecular informatics 37 (5), 1700078, 2018
Synthesis and anti-leukemic activity of pyrrolidinedione-thiazolidinone hybrids
A Kryshchyshyn, D Kaminskyy, O Roman, R Kralovics, O Karpenko, ...
Ukrainian Biochemical Journal 92 (2), 108-119, 2020
Synthesis and antitumor activity evaluation of 3,5a,6,11b-tetrahydro-2H,5H-chromeno[4',3':4,5]thiopyrano[2,3-d]thiazole derivatives (in Ukrainian)
AP Kryshchyshyn, ВS Zimenkovsky, LM Zaprutko, RВ Lesyk
Журнал органічної і фармацевтичної хімії/ Journal of organic and …, 2010
Thiazolidinone-Related Heterocyclic Compounds as Potential Antitrypanosomal Agents
A Kryshchyshyn, D Kaminskyy, P Grellier, R Lesyk
Azoles-Synthesis, Properties, Applications and Perspectives, 2020
Preliminary evaluation of thiazolidinone- and pyrazoline-related heterocyclic derivatives as potential antimalarial agents
A Kryshchyshyn-Dylevych, P Zelisko, Natalia: Grellier, R Lesyk
Biopolymers and Cell. 36 (1), 48-60, 2020
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