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Design, Synthesis, and Xanthine Oxidase Inhibitory Activity of 4‐(5‐Aminosubstituted‐4‐cyanooxazol‐2‐yl)benzoic Acids.
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- ChemMedChem, 2024, v. 19, n. 21, p. 1, doi. 10.1002/cmdc.202400478
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- Article
A Comparative In Vitro Anticancer Evaluation and In Silico Study of New 1‐(1,3‐Oxazol‐5‐yl)piperidine‐4‐sulfonylamides.
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- ChemistrySelect, 2024, v. 9, n. 41, p. 1, doi. 10.1002/slct.202403531
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- Article
New Sulfanilamide Derivatives Incorporating Heterocyclic Carboxamide Moieties as Carbonic Anhydrase Inhibitors.
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- Pharmaceuticals (14248247), 2021, v. 14, n. 8, p. 828, doi. 10.3390/ph14080828
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- Article
Intrinsic drug potential of oxazolo[5,4‐d]pyrimidines and oxazolo[4,5‐d]pyrimidines.
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- Chemical Biology & Drug Design, 2021, v. 98, n. 4, p. 561, doi. 10.1111/cbdd.13911
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- Article
In silico and in vitro studies of a number PILs as new antibacterials against MDR clinical isolate Acinetobacter baumannii.
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- Chemical Biology & Drug Design, 2020, v. 95, n. 6, p. 624, doi. 10.1111/cbdd.13678
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- Article
Rational design of isonicotinic acid hydrazide derivatives with antitubercular activity: Machine learning, molecular docking, synthesis and biological testing.
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- Chemical Biology & Drug Design, 2018, v. 92, n. 1, p. 1272, doi. 10.1111/cbdd.13188
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- Article
Chromene-Containing Aromatic Sulfonamides with Carbonic Anhydrase Inhibitory Properties.
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- International Journal of Molecular Sciences, 2021, v. 22, n. 10, p. 5082, doi. 10.3390/ijms22105082
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- Article
Theoretical and Experimental Studies of Phosphonium Ionic Liquids as Potential Antibacterials of MDR Acinetobacter baumannii.
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- Antibiotics (2079-6382), 2022, v. 11, n. 4, p. N.PAG, doi. 10.3390/antibiotics11040491
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- Article
Stability of fullerene complexes with oxazoles as biologically active compounds.
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- Applied Nanoscience, 2020, v. 10, n. 4, p. 1345, doi. 10.1007/s13204-019-01225-9
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- Article
New 2‐Oxoimidazolidine Derivatives: Design, Synthesis and Evaluation of Anti‐BK Virus Activities in Vitro.
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- Chemistry & Biodiversity, 2019, v. 16, n. 10, p. 1, doi. 10.1002/cbdv.201900391
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- Article
Synthesis, Characterization, In Vitro Anticancer Evaluation, ADMET Properties, and Molecular Docking of Novel 5‐Sulfanyl Substituted (Thiazol‐4‐yl)‐Phosphonium Salts.
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- ChemMedChem, 2024, v. 19, n. 18, p. 1, doi. 10.1002/cmdc.202400205
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- Article
Synthesis, characterization of novel N‐(4‐cyano‐1,3‐oxazol‐5‐yl)sulfonamide derivatives and in vitro screening their activity against NCI‐60 cancer cell lines.
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- ChemMedChem, 2024, v. 19, n. 5, p. 1, doi. 10.1002/cmdc.202300527
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- Article
Synthesis, Characterization and in vitro Anticancer Evaluation of 5‐Sulfinyl(sulfonyl)‐4‐arylsulfonyl‐Substituted 1,3‐Oxazoles.
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- ChemMedChem, 2023, v. 18, n. 14, p. 1, doi. 10.1002/cmdc.202300161
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- Article
Evaluation of Anticancer Activity of 1,3‐Oxazol‐4‐ylphosphonium Salts in Vitro.
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- ChemMedChem, 2022, v. 17, n. 20, p. 1, doi. 10.1002/cmdc.202200319
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Dependence of the anticancer activity of 1,3‐oxazole derivatives on the donor/acceptor nature of his substitues.
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- Journal of Heterocyclic Chemistry, 2019, v. 56, n. 11, p. 3122, doi. 10.1002/jhet.3711
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Hydroxamic Acids as PARP‐1 Inhibitors: Molecular Design and Anticancer Activity of Novel Phenanthridinones.
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- Helvetica Chimica Acta, 2023, v. 106, n. 10, p. 1, doi. 10.1002/hlca.202300133
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- Article
Synthesis, in silico and in vitro Evaluation of Novel Oxazolopyrimidines as Promising Anticancer Agents.
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- Helvetica Chimica Acta, 2020, v. 103, n. 12, p. 1, doi. 10.1002/hlca.202000169
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- Article
Functionalized 5‐Amino‐4‐cyanoxazoles, their Hetero‐ and Macrocyclic Derivatives: Preparation and Synthetic Applications.
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- European Journal of Organic Chemistry, 2021, v. 2021, n. 47, p. 6511, doi. 10.1002/ejoc.202100412
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- Article
Carbonic Anhydrase Inhibition with Sulfonamides Incorporating Pyrazole- and Pyridazinecarboxamide Moieties Provides Examples of Isoform-Selective Inhibitors.
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- Molecules, 2021, v. 26, n. 22, p. 7023, doi. 10.3390/molecules26227023
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- Article
Design of new imidazole derivatives with anti-HCMV activity: QSAR modeling, synthesis and biological testing.
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- Journal of Computer-Aided Molecular Design, 2021, v. 35, n. 12, p. 1177, doi. 10.1007/s10822-021-00428-z
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- Article
Synthesis and in vitro anticancer evaluation of functionalized 5-(4-piperazin-1-yl)-2-aryloxazoles and 5-[(4-arylsulfonyl)piperazin-1-yl]-2-phenyloxazoles.
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- Chemistry of Heterocyclic Compounds, 2024, v. 60, n. 1/2, p. 68, doi. 10.1007/s10593-024-03295-2
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- Article
Synthesis and in vitro anticancer potential of new thiazole-containing derivatives of rhodanine.
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- Chemistry of Heterocyclic Compounds, 2023, v. 59, n. 6/7, p. 484, doi. 10.1007/s10593-023-03220-z
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New oxazole to oxazole recyclization.
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- Chemistry of Heterocyclic Compounds, 2023, v. 59, n. 6/7, p. 521, doi. 10.1007/s10593-023-03226-7
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Parent 5(7)-azachromones and their partially hydrogenated derivatives: synthesis and physicochemical properties.
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- Chemistry of Heterocyclic Compounds, 2023, v. 59, n. 6/7, p. 494, doi. 10.1007/s10593-023-03221-y
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- Article
Condensed azole-based organophosphorus heterocycles.
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- Chemistry of Heterocyclic Compounds, 2023, v. 59, n. 4/5, p. 217, doi. 10.1007/s10593-023-03184-0
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In silico Study of Conjugated Nitrogen Heterocycles Affinity in their Biological Complexes.
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- Chemistry of Heterocyclic Compounds, 2022, v. 58, n. 8/9, p. 412, doi. 10.1007/s10593-022-03107-5
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- Article
Synthesis of new antineoplastic agents based on imidazo[2,1-a]pyridine.
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- Chemistry of Heterocyclic Compounds, 2020, v. 56, n. 11, p. 1460, doi. 10.1007/s10593-020-02838-7
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- Article
Synthesis of imidazo[2,1-b][1,3]thiazoles – potential anticancer agents derived from γ-bromodipnones.
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- Chemistry of Heterocyclic Compounds, 2020, v. 56, n. 8, p. 1073, doi. 10.1007/s10593-020-02776-4
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- Article
3-Hetarylisocoumarins in the synthesis of 1-functionalized 3-hetarylisoquinolines.
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- Chemistry of Heterocyclic Compounds, 2020, v. 56, n. 8, p. 1021, doi. 10.1007/s10593-020-02769-3
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- Article
Strategy for the synthesis of 2,2-disubstituted 8-azachromanones via Horner–Wadsworth–Emmons olefination.
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- Chemistry of Heterocyclic Compounds, 2020, v. 56, n. 2, p. 213, doi. 10.1007/s10593-020-02646-z
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- Article
In vitro Activity of Novel 1,3-Oxazole Derivatives against Human Papillomavirus.
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- Ibnosina Journal of Medicine & Biomedical Sciences, 2017, v. 9, n. 4, p. 11, doi. 10.4103/ijmbs.ijmbs_9_17
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Interactions of 3‐Acylisocoumarins with Ethane‐1,2‐diamines: A Simple Route to 3,4‐Dihydro‐6H‐pyrazino[1,2‐b]isoquinolin‐6‐ones and Their Hydrogenated Derivatives.
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- ChemistrySelect, 2024, v. 9, n. 40, p. 1, doi. 10.1002/slct.202403740
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Distinctive Features of 3‐Acetyl‐ and 3‐Benzoyl‐Isocoumarins' Interaction with Active Primary Amines.
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- ChemistrySelect, 2023, v. 8, n. 37, p. 1, doi. 10.1002/slct.202301380
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- Article
Recyclization of 5‐Amino‐ oxazoles as a Route to new Functionalized Heterocycles (Developments of V.P. Kukhar Institute of Bioorganic Chemistry and Petrochemistry of the NAS of Ukraine).
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- Chemical Record, 2024, v. 24, n. 2, p. 1, doi. 10.1002/tcr.202300264
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- Article
Enhancing Sorghum Productivity with Methyur, Kamethur, and Ivin Plant Growth Regulators †.
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- Biology & Life Sciences Forum, 2023, v. 27, p. 36, doi. 10.3390/IECAG2023-15222
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In Silico Design and Experimental Validation of Novel Oxazole Derivatives Against Varicella zoster virus.
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- Molecular Biotechnology, 2024, v. 66, n. 4, p. 707, doi. 10.1007/s12033-023-00670-w
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- Article
Rapid synthetic approaches to libraries of diversified 1,2-dihydrochromeno[2,3-c]pyrrole-3,9-diones and 3-(2-hydroxyphenyl)-4,5-dihydropyrrolo[3,4-c]pyrazol-6(1H)-ones.
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- Molecular Diversity, 2022, v. 26, n. 2, p. 1115, doi. 10.1007/s11030-021-10234-2
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Synthesis of some oxazolo[4,5-d]pyrimidine derivatives and evaluation of their antiviral activity and cytotoxicity.
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- ARKIVOC: Online Journal of Organic Chemistry, 2022, v. 2022, p. 108, doi. 10.24820/ark.5550190.p011.693
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Concise and regioselective synthesis of 5H-imidazo[1,2-e][1,3,5]triazepines.
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- ARKIVOC: Online Journal of Organic Chemistry, 2022, v. 2022, p. 204, doi. 10.24820/ark.5550190.p011.689
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1H-isochromene-1-ones and isoquinoline-1(2H)-ones with carbonyl group in position 3: Features of synthetic approaches and transformation.
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- ARKIVOC: Online Journal of Organic Chemistry, 2022, v. 2022, p. 79, doi. 10.24820/ark.5550190.p011.861
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- Article