Search Results - "Smolii, Oleg B"

Express Method for Isolation of Ready-to-Use 3D Chitin Scaffolds from Aplysina archeri (Aplysineidae: Verongiida) Demosponge by Klinger, Christine, Żółtowska-Aksamitowska, Sonia, Wysokowski, Marcin, Tsurkan, Mikhail V, Galli, Roberta, Petrenko, Iaroslav, Machałowski, Tomasz, Ereskovsky, Alexander, Martinović, Rajko, Muzychka, Lyubov, Smolii, Oleg B, Bechmann, Nicole, Ivanenko, Viatcheslav, Schupp, Peter J, Jesionowski, Teofil, Giovine, Marco, Joseph, Yvonne, Bornstein, Stefan R, Voronkina, Alona, Ehrlich, Hermann

“…Sponges are a valuable source of natural compounds and biomaterials for many biotechnological applications. Marine sponges belonging to the order Verongiida…”
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Naturally Prefabricated Marine Biomaterials: Isolation and Applications of Flat Chitinous 3D Scaffolds from Ianthella labyrinthus (Demospongiae: Verongiida) by Schubert, Mario, Binnewerg, Björn, Voronkina, Alona, Muzychka, Lyubov, Wysokowski, Marcin, Petrenko, Iaroslav, Kovalchuk, Valentine, Tsurkan, Mikhail, Martinovic, Rajko, Bechmann, Nicole, Ivanenko, Viatcheslav N, Fursov, Andriy, Smolii, Oleg B, Fromont, Jane, Joseph, Yvonne, Bornstein, Stefan R, Giovine, Marco, Erpenbeck, Dirk, Guan, Kaomei, Ehrlich, Hermann

“…Marine sponges remain representative of a unique source of renewable biological materials. The demosponges of the family Ianthellidae possess chitin-based…”
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Naturally Drug-Loaded Chitin: Isolation and Applications by Kovalchuk, Valentine, Voronkina, Alona, Binnewerg, Björn, Schubert, Mario, Muzychka, Liubov, Wysokowski, Marcin, Tsurkan, Mikhail V, Bechmann, Nicole, Petrenko, Iaroslav, Fursov, Andriy, Martinovic, Rajko, Ivanenko, Viatcheslav N, Fromont, Jane, Smolii, Oleg B, Joseph, Yvonne, Giovine, Marco, Erpenbeck, Dirk, Gelinsky, Michael, Springer, Armin, Guan, Kaomei, Bornstein, Stefan R, Ehrlich, Hermann

“…Naturally occurring three-dimensional (3D) biopolymer-based matrices that can be used in different biomedical applications are sustainable alternatives to…”
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New Source of 3D Chitin Scaffolds: The Red Sea Demosponge Pseudoceratina arabica (Pseudoceratinidae, Verongiida) by Shaala, Lamiaa A, Asfour, Hani Z, Youssef, Diaa T A, Żółtowska-Aksamitowska, Sonia, Wysokowski, Marcin, Tsurkan, Mikhail, Galli, Roberta, Meissner, Heike, Petrenko, Iaroslav, Tabachnick, Konstantin, Ivanenko, Viatcheslav N, Bechmann, Nicole, Muzychka, Lyubov V, Smolii, Oleg B, Martinović, Rajko, Joseph, Yvonne, Jesionowski, Teofil, Ehrlich, Hermann

“…The bioactive bromotyrosine-derived alkaloids and unique morphologically-defined fibrous skeleton of chitin origin have been found recently in marine…”
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Synthesis and in vitro evaluation of antibacterial and antibiofilm activities of novel triphenylphosphonium‐functionalized substituted pyrimidines by Muzychka, Liubov V., Humeniuk, Nataliia I., Boiko, Iryna O., Vrynchanu, Nina O., Smolii, Oleg B.

“…The increase in the prevalence of antibiotic‐resistant pathogens leads to a decrease in the number of antimicrobial agents for the treatment of infections and…”
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Marine biomimetics: bromotyrosines loaded chitinous skeleton as source of antibacterial agents by Muzychka, Liubov, Voronkina, Alona, Kovalchuk, Valentine, Smolii, Oleg B., Wysokowski, Marcin, Petrenko, Iaroslav, Youssef, Diaa T. A., Ehrlich, Irina, Ehrlich, Hermann

“…The marine sponges of the order Verongiida (Demospongiae: Porifera) have survived on our planet for more than 500 million years due to the presence of a unique…”
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Synthesis, QSAR modeling, and molecular docking of novel fused 7‐deazaxanthine derivatives as adenosine A2A receptor antagonists by Muzychka, Liubov V., Verves, Evgenii V., Yaremchuk, Iryna O., Zinchenko, Anna M., Shishkina, Svitlana V., Semenyuta, Ivan V., Hodyna, Diana M., Metelytsia, Larysa O., Kovalishyn, Vasyl, Smolii, Oleg B.

“…Predictive QSAR models for the search of new adenosine A2A receptor antagonists were developed by using OCHEM platform. The predictive ability of the…”
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One‐Pot Synthesis of 6‐Aminopyrido[2,3‐d]pyrimidin‐7‐ones by Zinchenko, Anna M., Muzychka, Lyubov V., Kucher, Olexandr V., Sadkova, Iryna V., Mykhailiuk, Pavel K., Smolii, Oleg B.

“…One‐pot synthesis of 6‐aminopyrido[2,3‐d]pyrimidin‐7‐ones from 4‐aminopyrimidine‐5‐carbaldehydes and the in situ N‐protected methyl glycinate is developed. The…”
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Synthesis, QSAR modeling, and molecular docking of novel fused 7-deazaxanthine derivatives as adenosine A 2A receptor antagonists by Muzychka, Liubov V, Verves, Evgenii V, Yaremchuk, Iryna O, Zinchenko, Anna M, Shishkina, Svitlana V, Semenyuta, Ivan V, Hodyna, Diana M, Metelytsia, Larysa O, Kovalishyn, Vasyl, Smolii, Oleg B

“…Predictive QSAR models for the search of new adenosine A receptor antagonists were developed by using OCHEM platform. The predictive ability of the regression…”
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Synthesis and reactions of novel imidazo[4,5-b]pyridine building blocks by Dubina, Tetiana F., Kosarevych, Anton V., Kucher, Olexandr V., Sosunovych, Bohdan S., Smolii, Oleg B., Vashchenko, Bohdan V., Grygorenko, Oleksandr O.

“…The synthesis of a novel imidazo[4,5- b ]pyridine and its partially saturated derivative relied on Michael addition of 1-methyl-1 H -imidazol-4-amine to…”
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Pyrrolo[2,3-d]pyrimidine derivatives in the synthesis of a novel heterocyclic system 2a,5a,7-triazaacenaphthylene by Muzychka, Lyubov V., Yaremchuk, Iryna O., Verves, Evgenii V., Smolii, Oleg B.

“…A convenient method for the synthesis of methyl 8-oxo-3 H ,8 H -2a,5a,7-triazaacenaphthylene-2-carboxylate by iodination of 7-allyl-4-methoxypyrrolo[2,3- d…”
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Enzyme-Catalyzed Kinetic Resolution of 2,2,2-Trifluoro-1-(heteroaryl)ethanols: Experimental and Docking Studies by Kucher, Olexandr V., Kolodiazhnaya, Anastasiya O., Smolii, Oleg B., Prisuazhnyk, Dmytro V., Tolmacheva, Katerina A., Zaporozhets, Olga A., Moroz, Yurii S., Mykhailiuk, Pavel K., Tolmachev, Andrey A.

“…A convenient approach towards enantiopure (R) and (S) isomers of 2,2,2‐trifluoro‐1‐(heteroaryl)ethanols was developed. The enzyme‐catalyzed kinetic resolution…”
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Synthesis of new 4-amino-substituted 7-iminopyrido[2,3-d]pyrimidines by Zinchenko, Anna N., Muzychka, Lyubov V., Biletskii, Igor I., Smolii, Oleg B.

“…The reaction of 4,6-dichloropyrimidine-5-carbaldehyde with cyanomethyltriphenylphosphonium chloride gave (2 Е )-3-(4,6-dichloropyrimidin-5-yl)acrylonitrile,…”
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Marine biomaterials: Biomimetic and pharmacological potential of cultivated Aplysina aerophoba marine demosponge by Binnewerg, Björn, Schubert, Mario, Voronkina, Alona, Muzychka, Liubov, Wysokowski, Marcin, Petrenko, Iaroslav, Djurović, Mirko, Kovalchuk, Valentine, Tsurkan, Mikhail, Martinovic, Rajko, Bechmann, Nicole, Fursov, Andriy, Ivanenko, Viatcheslav N., Tabachnick, Konstantin R., Smolii, Oleg B., Joseph, Yvonne, Giovine, Marco, Bornstein, Stefan R., Stelling, Allison L., Tunger, Antje, Schmitz, Marc, Taniya, Olga S., Kovalev, Igor S., Zyryanov, Grigory V., Guan, Kaomei, Ehrlich, Hermann

“…Marine demosponges of the Verongiida order are considered a gold-mine for bioinspired materials science and marine pharmacology. The aim of this work was to…”
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Crystal structure of ( S )-1-(1,3-benzothiazol-2-yl)-2,2,2-trifluoroethanol by Shishkina, Svitlana V., Kucher, Olexandr V., Kolodiazhnaya, Anastasiya O., Smolii, Oleg B., Tolmachev, Andrey A.

“…In the title compound, C 9 H 6 F 3 NOS, the 1,3-benzothiazole ring system is essentially planar, with an r.m.s. deviation of 0.006 Å. In the crystal, molecules…”
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Synthesis and enzymatic resolution of novel analogs of alicyclic and heterocyclic mandelic acid derivatives by Sosunovych, Bohdan S., Timokhin, Oleksii S., Kucher, Olexandr V., Demianyk, Nadiia Y., Hys, Denys V., Zvarych, Yelyzaveta A., Smolii, Oleg B., Vashchenko, Bohdan V., Grygorenko, Oleksandr O.

“…Synthesis and enzymatic resolution of a new class of alicyclic and heterocyclic mandelic acid derivatives was described. The method relied on the preparation…”
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Synthesis of novel 1,2-dihydropyrrolo[1,2-a]pyrazin-1(2H)-one derivatives by Yaremchuk, Iryna O., Muzychka, Lyubov V., Smolii, Oleg B., Kucher, Olexandr V., Shishkina, Svitlana V.

“…[Display omitted] •Wide range of novel 1,2-dihydropyrrolo[1,2-a]pyrazin-1(2H)-ones was synthesized.•The mechanism of oxazine to pyrazine transformation was…”
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Lipase kinetic enantiomeric resolution of 1-heteroarylethanols by Kucher, Olexandr V., Kolodyazhnaya, Anastasiya O., Smolii, Oleg B., Nazarenko, Nadiya K., Kubyshkin, Vladimir, Mykhailiuk, Pavel K., Tolmachev, Andrey A.

“…[Display omitted] The use of lipases offers a simple and straightforward method toward various chiral secondary alcohols. Here we examined the lipase…”
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Crystal structure of (S)-1-(1,3-benzo-thia-zol-2-yl)-2,2,2-tri-fluoro-ethanol by Shishkina, Svitlana V, Kucher, Olexandr V, Kolodiazhnaya, Anastasiya O, Smolii, Oleg B, Tolmachev, Andrey A

“…In the title compound, C9H6F3NOS, the 1,3-benzo-thia-zole ring system is essentially planar, with an r.m.s. deviation of 0.006 Å. In the crystal, mol-ecules…”
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Enzymatic resolution of chroman-4-ol and its core analogues with Burkholderia cepacia lipase by Kucher, Olexandr V., Kolodyazhnaya, Anastasiya O., Smolii, Oleg B., Boiko, Alexandr I., Kubyshkin, Vladimir S., Mykhailiuk, Pavel K., Tolmachev, Andrey A.

“…A convenient protocol for lipase resolution of chroman-4-ol and its analogues (six- and seven-membered rings with O, S, SO2) has been elaborated. The structure…”
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