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Oral Bioavailability and Pharmacokinetics of Nonanimal Chondroitin Sulfate and Its Constituents in Healthy Male Volunteers.
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- Clinical Pharmacology in Drug Development, 2019, v. 8, n. 3, p. 336, doi. 10.1002/cpdd.587
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- Article
Methylphenidate Analogues as a New Class of Potential Disease-Modifying Agents for Parkinson's Disease: Evidence from Cell Models and Alpha-Synuclein Transgenic Mice.
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- Pharmaceutics, 2022, v. 14, n. 8, p. 1595, doi. 10.3390/pharmaceutics14081595
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- Article
Benzodioxane–Benzamides as FtsZ Inhibitors: Effects of Linker's Functionalization on Gram-Positive Antimicrobial Activity.
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- Antibiotics (2079-6382), 2023, v. 12, n. 12, p. 1712, doi. 10.3390/antibiotics12121712
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Computational Design and Development of Benzodioxane-Benzamides as Potent Inhibitors of FtsZ by Exploring the Hydrophobic Subpocket.
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- Antibiotics (2079-6382), 2021, v. 10, n. 4, p. 442, doi. 10.3390/antibiotics10040442
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- Article
Staphylococcus aureus RnpA Inhibitors: Computational-Guided Design, Synthesis and Initial Biological Evaluation.
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- Antibiotics (2079-6382), 2021, v. 10, n. 4, p. 438, doi. 10.3390/antibiotics10040438
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- Article
Benzamide Derivatives Targeting the Cell Division Protein FtsZ: Modifications of the Linker and the Benzodioxane Scaffold and Their Effects on Antimicrobial Activity.
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- Antibiotics (2079-6382), 2020, v. 9, n. 4, p. 160, doi. 10.3390/antibiotics9040160
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- Article
Targeting Bacterial Cell Division: A Binding Site-Centered Approach to the Most Promising Inhibitors of the Essential Protein FtsZ.
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- Antibiotics (2079-6382), 2020, v. 9, n. 2, p. 69, doi. 10.3390/antibiotics9020069
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- Article
Corrigendum: Design and Synthesis of Fluorescent Methylphenidate Analogues for a FRET‐Based Assay of Synapsin III Binding.
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- ChemMedChem, 2022, v. 17, n. 13, p. 1, doi. 10.1002/cmdc.202200243
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- Article
Design and Synthesis of Fluorescent Methylphenidate Analogues for a FRET‐Based Assay of Synapsin III Binding.
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- ChemMedChem, 2020, v. 15, n. 14, p. 1330, doi. 10.1002/cmdc.202000128
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- Article
Benzodioxane‐Benzamides as Antibacterial Agents: Computational and SAR Studies to Evaluate the Influence of the 7‐Substitution in FtsZ Interaction.
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- ChemMedChem, 2020, v. 15, n. 2, p. 195, doi. 10.1002/cmdc.201900537
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- Article
2-(1-Methoxycarbonyl-2-phenyleth-1-yl)-1-benzylpyridin-1-ium Bromide.
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- Molbank, 2023, v. 2023, n. 4, p. M1738, doi. 10.3390/M1738
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- Article
Obtainment of Threo and Erythro Isomers of the 6-Fluoro-3-(2,3,6,7,8,9-hexahydronaphtho[2,3- b ][1,4]dioxin-2-yl)-2,3-dihydrobenzo[ b ][1,4]dioxine-5-carboxamide.
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- Molbank, 2023, v. 2023, n. 1, p. M1559, doi. 10.3390/M1559
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- Article
(3-Methylene-2,3-dihydronaphtho[2,3- b ][1,4]dioxin-2-yl)methanol.
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- Molbank, 2022, v. 2022, n. 4, p. M1521, doi. 10.3390/M1521
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- Article
Physical Properties of Sulpiride and Its (S)-Enantiomer Physikalische Eigenschaften von Sulpirid und seinem (S)-Enantiomer.
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- Archiv der Pharmazie, 1987, v. 320, n. 9, p. 859, doi. 10.1002/ardp.19873200916
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- Article
Resolution via diastereomeric amides of enantiopure 1,4‐benzoxathian‐2‐ and 3‐carboxylic acids and determination of their configuration.
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- Chirality, 2022, v. 34, n. 8, p. 1053, doi. 10.1002/chir.23474
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- Article
How do reaction conditions affect the enantiopure synthesis of 2‐substituted‐1,4‐benzodioxane derivatives?
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- Chirality, 2018, v. 30, n. 7, p. 943, doi. 10.1002/chir.22968
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- Article
Predicting the physicochemical profile of diastereoisomeric histidine-containing dipeptides by property space analysis.
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- Chirality, 2012, v. 24, n. 7, p. 566, doi. 10.1002/chir.22056
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- Article
2,6-Difluorobenzamide Inhibitors of Bacterial Cell Division Protein FtsZ: Design, Synthesis, and Structure-Activity Relationships.
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- ChemMedChem, 2017, v. 12, n. 16, p. 1303, doi. 10.1002/cmdc.201700201
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- Article
Inside Cover: 2,6-Difluorobenzamide Inhibitors of Bacterial Cell Division Protein FtsZ: Design, Synthesis, and Structure-Activity Relationships (ChemMedChem 16/2017).
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- ChemMedChem, 2017, v. 12, n. 16, p. 1225, doi. 10.1002/cmdc.201700471
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- Article
Asymmetric Aldol Condensation of 1-Naphtol and Pyruvates in the Presence of Lewis Acids Preliminary Communication.
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- Helvetica Chimica Acta, 1984, v. 67, n. 3, p. 739, doi. 10.1002/hlca.19840670313
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- Article