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Targeting Biometals in Alzheimer's Disease with Metal Chelating Agents Including Coumarin Derivatives.
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- CNS Drugs, 2024, v. 38, n. 7, p. 507, doi. 10.1007/s40263-024-01093-0
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Evaluation of Cytotoxicity and Apoptosis Induced by Coumarin Hydrazide-Hydrazone Derivatives in Human Hepatocellular Carcinoma Cell Line.
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- Trends in Sciences, 2024, v. 21, n. 7, p. 1, doi. 10.48048/tis.2024.7628
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Synthesis of 2,3‐Diarylindanones and 2‐Arylindenes from Trisubstituted α,β‐Unsaturated Esters Derived from Highly Strained 2,3‐Diarylcyclopropenones by Ring Opening with Coumarin Derivatives.
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- European Journal of Organic Chemistry, 2024, v. 27, n. 24, p. 1, doi. 10.1002/ejoc.202400036
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Editorial: Chemistry, toxicity, synthesis, biological and pharmacological activities of coumarins and their derivatives: recent advances and future perspectives.
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- Frontiers in Pharmacology, 2024, p. 1, doi. 10.3389/fphar.2024.1430985
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Fishing antioxidant 4-hydroxycoumarin derivatives: synthesis, characterization, and in vitro assessments.
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- Canadian Journal of Physiology & Pharmacology, 2024, v. 102, n. 6, p. 361, doi. 10.1139/cjpp-2023-0455
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Coumarin‐Based Light‐Responsive Composite Nanochannel Membranes for Precise Controlled Release of Pesticides.
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- Advanced Functional Materials, 2024, v. 34, n. 21, p. 1, doi. 10.1002/adfm.202314642
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MULTICOMPONENT REACTIONS OF CYANOACETANILIDE DERIVATIVES: SYNTHESIS OF COUMARIN AND QUINOLINE DERIVATIVE AND EVALUATIONS OF THEIR CYTOTOXICITY.
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- Bulletin of the Chemical Society of Ethiopia, 2024, v. 38, n. 3, p. 739, doi. 10.4314/bcse.v38i3.15
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Insights on Stability Constants and Structures of Complexes between Coumarin Derivatives and Pb(II) in Aqueous Media.
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- Molecules, 2024, v. 29, n. 9, p. 1911, doi. 10.3390/molecules29091911
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- Article
Synthesis, biofilm formation inhibitory, and inflammation inhibitory activities of new coumarin derivatives.
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- Scientific Reports, 2024, v. 14, n. 1, p. 1, doi. 10.1038/s41598-024-59072-w
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- Article
Synthesis, Characterization, and Photophysical Properties of 2-Quinolone-Based Compounds.
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- Duzce University Journal of Science & Technology, 2024, v. 12, n. 2, p. 642, doi. 10.29130/dubited.1377215
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- Article
Synergistic Biomedical Potential and Molecular Docking Analyses of Coumarin–Triazole Hybrids as Tyrosinase Inhibitors: Design, Synthesis, In Vitro Profiling, and In Silico Studies.
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- Pharmaceuticals (14248247), 2024, v. 17, n. 4, p. 532, doi. 10.3390/ph17040532
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Design, Synthesis, and Biological Evaluation of Novel Coumarin Analogs Targeted against SARS-CoV-2.
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- Molecules, 2024, v. 29, n. 6, p. 1406, doi. 10.3390/molecules29061406
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- Article
Synthesis and evaluation of coumarin derivatives on antioxidative, tyrosinase inhibitory activities, melanogenesis, and in silico investigations.
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- Scientific Reports, 2024, v. 14, n. 1, p. 1, doi. 10.1038/s41598-024-54665-x
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Synthesis, characterization, antimicrobial activity and molecular docking study of transition metal complexes based on azo coumarin and thiosemicarbazone derivative.
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- Journal of the Iranian Chemical Society, 2024, v. 21, n. 3, p. 719, doi. 10.1007/s13738-023-02953-0
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- Article
Coumarin Derivatives: The Influence of Cycloalkyl Groups at the C-3 Position on Intermolecular Interactions—Synthesis, Structure and Spectroscopy.
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- Crystals (2073-4352), 2024, v. 14, n. 2, p. 196, doi. 10.3390/cryst14020196
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New Pd(II) complexes containing hydrazinyl oxazolyl coumarin derivatives: synthesis, spectral characterization and anti-cancer studies.
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- Zeitschrift für Physikalische Chemie, 2024, v. 238, n. 2, p. 261, doi. 10.1515/zpch-2023-0380
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- Article
Iridoid Glycosides and Coumarin Glycoside Derivatives from the Roots of Nymphoides peltata and Their In Vitro Wound Healing Properties.
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- International Journal of Molecular Sciences, 2024, v. 25, n. 2, p. 1268, doi. 10.3390/ijms25021268
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Theoretical study of the stability and reactivity of nitro-coumarins and amino-coumarins by DFT method.
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- Theoretical Chemistry Accounts: Theory, Computation, & Modeling, 2024, v. 143, n. 1, p. 1, doi. 10.1007/s00214-023-03079-5
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- Article
Transcriptional insights of citrus defense response against Diaporthe citri.
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- BMC Plant Biology, 2023, v. 23, n. 1, p. 1, doi. 10.1186/s12870-023-04624-x
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- Article
Transcriptional insights of citrus defense response against Diaporthe citri.
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- BMC Plant Biology, 2023, v. 23, n. 1, p. 1, doi. 10.1186/s12870-023-04624-x
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- Article
Transcriptional insights of citrus defense response against Diaporthe citri.
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- BMC Plant Biology, 2023, v. 23, n. 1, p. 1, doi. 10.1186/s12870-023-04624-x
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- Article
Design, Synthesis, and Anticancer of Some New Amide Derivatives from Coumarin-3-Carboxylic Acid Combined with Carbohydrate.
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- Egyptian Academic Journal of Biological Sciences, C Physiology & Molecular Biology, 2023, v. 15, n. 2, p. 37, doi. 10.21608/EAJBSC.2023.308857
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- Article
Photocatalytic Synthesis of Coumarin Derivatives Using Visible-Light-Responsive Strawberry Dye-Sensitized Titanium Dioxide Nanoparticles.
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- Nanomaterials (2079-4991), 2023, v. 13, n. 23, p. 3001, doi. 10.3390/nano13233001
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Coumarin: A Renowned Moiety for Gram-Negative Escherichia coli – a Review.
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- Pharmaceutical Chemistry Journal, 2023, v. 57, n. 8, p. 1230, doi. 10.1007/s11094-024-03033-0
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- Article
Novel Coumarin Derivatives as Potential Urease Inhibitors for Kidney Stone Prevention and Antiulcer Therapy: From Synthesis to In Vivo Evaluation.
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- Pharmaceuticals (14248247), 2023, v. 16, n. 11, p. 1552, doi. 10.3390/ph16111552
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- Article
Synthesis of New of 4-Thiazolidinone and Thiazole Derivatives Containing Coumarin Moiety with Antimicrobial Activity.
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- Acta Chimica Slovenica, 2023, v. 70, n. 4, p. 500, doi. 10.17344/acsi.2023.8281
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- Article
Coumarin N -Acylhydrazone Derivatives: Green Synthesis and Antioxidant Potential—Experimental and Theoretical Study.
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- Antioxidants, 2023, v. 12, n. 10, p. 1858, doi. 10.3390/antiox12101858
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- Article
DESIGN, SYNTHESIS, AND CYTOTOXIC ACTIVITY OF SOME NOVEL N-(SUBSTITUTED) BENZAMIDE DERIVATIVES BEARING COUMARIN AND 1-AZOCOUMARIN COMPOUNDS.
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- Bulletin of the Chemical Society of Ethiopia, 2023, v. 37, n. 4, p. 1003, doi. 10.4314/bcse.v37i4.16
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Determining the 3-substituted Coumarins inhibitory potential against the HslV protease of E. coli.
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- European Review for Medical & Pharmacological Sciences, 2023, v. 27, n. 19, p. 9169
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- Article
Synthesis and Study of Copolymers Bearing Two Coumarin Side Groups in Monomer Unit: Toward Photoalignment of Liquid Crystals.
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- Macromolecular Chemistry & Physics, 2023, v. 224, n. 19, p. 1, doi. 10.1002/macp.202300191
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Coumarins from Jinhua Finger Citron: Separation by Liquid–Liquid Chromatography and Potential Antitumor Activity.
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- Molecules, 2023, v. 28, n. 19, p. 6917, doi. 10.3390/molecules28196917
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Review on the protective activity of osthole against the pathogenesis of osteoporosis.
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- Frontiers in Pharmacology, 2023, p. 1, doi. 10.3389/fphar.2023.1236893
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- Article
Apoptosis Induction by New Coumarin Derivatives in a Mice Model of Breast Cancer.
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- Archives of Razi Institute, 2023, v. 78, n. 5, p. 1430, doi. 10.32592/ari.2023.78.5.1430
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Synthesis and anti‐parasites efficacy of coumarin derivatives against Dactylogyrus intermedius.
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- Journal of Fish Diseases, 2023, v. 46, n. 9, p. 967, doi. 10.1111/jfd.13817
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- Article
Synthesis and Biological Evaluation of Substituted Fused Dipyranoquinolinones.
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- Organics, 2023, v. 4, n. 3, p. 364, doi. 10.3390/org4030027
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- Article
Evaluation of Anti-Inflammatory and Anti-Tubercular Activity of 4-Methyl-7-Substituted Coumarin Hybrids and Their Structure Activity Relationships.
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- Pharmaceuticals (14248247), 2023, v. 16, n. 9, p. 1326, doi. 10.3390/ph16091326
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- Article
Detection of Coumarin Derivatives of Viola odorata Cultivated in Iraq.
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- Journal of Pharmacy & Bioallied Sciences, 2023, v. 15, p. S948, doi. 10.4103/jpbs.jpbs_270_23
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- Article
Synthesis of New Coumarin Scaffold Bearing 2-Iminochromene Moiety.
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- Acta Chimica Slovenica, 2023, v. 70, n. 3, p. 380, doi. 10.17344/acsi.2023.8016
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- Article
Visible‐Light‐Active Coumarin‐ and Quinolinone‐Based Photocatalysts and Their Applications in Chemical Transformations.
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- Chemical Record, 2023, v. 23, n. 7, p. 1, doi. 10.1002/tcr.202200267
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- Article
Novel 3-Substituted 8-Methoxycoumarin Derivatives as Anti-Breast Cancer Drugs.
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- Crystals (2073-4352), 2023, v. 13, n. 7, p. 1037, doi. 10.3390/cryst13071037
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- Article
Effect of further substitutions at 5-, 6-, 7-, or 8-position of 3-[3-(4-methoxyphenyl)-1-hydroxyprop-2-yl]coumarin on phytotoxicity.
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- Journal of Pesticide Science, 2023, v. 48, n. 3, p. 93, doi. 10.1584/jpestics.D23-016
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- Article
Biogenic CuO NPs for synthesis of coumarin derivatives in hydrotropic aqueous medium.
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- Research on Chemical Intermediates, 2023, v. 49, n. 7, p. 2989, doi. 10.1007/s11164-023-05034-2
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- Article
Levandule lékařská - představení léčivé a aromatické rostliny.
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- Výživa a Potraviny, 2023, n. 4, p. 2
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- Article
Synthesis and Biological Properties of Pyranocoumarin Derivatives as Potent Anti-Inflammatory Agents.
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- International Journal of Molecular Sciences, 2023, v. 24, n. 12, p. 10026, doi. 10.3390/ijms241210026
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- Article
4-Methylumbelliferone enhances the effects of chemotherapy on both temozolomide-sensitive and resistant glioblastoma cells.
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- Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-35045-3
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- Article
6-Methylcoumarin Promotes Melanogenesis through the PKA/CREB, MAPK, AKT/PI3K, and GSK3β/β-Catenin Signaling Pathways.
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- Molecules, 2023, v. 28, n. 11, p. 4551, doi. 10.3390/molecules28114551
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- Article
Pharmacological Potential of Coumarin-Based Derivatives: (A Comprehensive Brief Review).
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- Oriental Journal of Chemistry, 2023, v. 39, n. 3, p. 568, doi. 10.13005/ojc/390304
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- Article
Two New Coumarins with Immunomodulatory and Anticancer Activities from Sterculia colorata.
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- Chemistry of Natural Compounds, 2023, v. 59, n. 3, p. 436, doi. 10.1007/s10600-023-04018-3
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- Article
Coumarin derivatives with potential anticancer and antibacterial activity: Design, synthesis, VEGFR‐2 and DNA gyrase inhibition, and in silico studies.
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- Drug Development Research, 2023, v. 84, n. 3, p. 433, doi. 10.1002/ddr.22037
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Pharmacological Advances of Coumarin and Its Derivatives.
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- Indian Journal of Pharmaceutical Sciences, 2023, v. 85, n. 3, p. 565, doi. 10.36468/pharmaceutical-sciences.1124
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- Article