Works about COUMARINS
Results: 3213
Zebrafish as a Suitable Model for Utilizing the Bioactivity of Coumarins and Coumarin-Based Compounds.
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- International Journal of Molecular Sciences, 2025, v. 26, n. 4, p. 1444, doi. 10.3390/ijms26041444
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Playing Around the Coumarin Core in the Discovery of Multimodal Compounds Directed at Alzheimer's-Related Targets: A Recent Literature Overview.
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- Molecules, 2025, v. 30, n. 4, p. 891, doi. 10.3390/molecules30040891
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Identification and Quantification of Total Coumarins from Urtica dentata Hand and Its Roles in Promoting Immune Tolerance via TLR4-Mediated Dendritic Cell Immaturation.
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- Bioscience, Biotechnology & Biochemistry, 2013, v. 77, n. 6, p. 1200, doi. 10.1271/bbb.120958
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Characterization of Coumarin-Specific Prenyltransferase Activities in Citrus limon Peel.
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- Bioscience, Biotechnology & Biochemistry, 2012, v. 76, n. 7, p. 1389, doi. 10.1271/bbb.120192
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Biosynthesis of Coumarin Glycosides by Transgenic Hairy Roots of Polygonum multiflorum.
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- Bioscience, Biotechnology & Biochemistry, 2012, v. 76, n. 5, p. 1008, doi. 10.1271/bbb.110347
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Coumarins from Clausena anisum-olens Merr.
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- Bioscience, Biotechnology & Biochemistry, 2010, v. 74, n. 7, p. 1483, doi. 10.1271/bbb.100143
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Effects of Osthole on Migration and Invasion in Breast Cancer Cells.
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- Bioscience, Biotechnology & Biochemistry, 2010, v. 74, n. 7, p. 1430, doi. 10.1271/bbb.100110
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Kinetic Characterization of the Oxidation of Esculetin by Polyphenol Oxidase and Peroxidase.
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- Bioscience, Biotechnology & Biochemistry, 2007, v. 71, n. 2, p. 390, doi. 10.1271/bbb.60431
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Glucosylation of Phenolic Compounds by Pharbitis nil Hairy Roots: I. Glucosylation of Coumarin and Flavone Derivatives.
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- Bioscience, Biotechnology & Biochemistry, 2004, v. 68, n. 10, p. 2032, doi. 10.1271/bbb.68.2032
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Catalytic Reaction of Basiodiomycete Lentinula edodes Cytochrome P450, Le.CYP1 Enzyme Produced in Yeast.
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- Bioscience, Biotechnology & Biochemistry, 2004, v. 68, n. 1, p. 79, doi. 10.1271/bbb.68.79
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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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Coumarin Grafted Polyethylene Matrix as Colorimetric and Fluorescent Chemosensor for Metal Ions.
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- Macromolecular Chemistry & Physics, 2020, v. 221, n. 21, p. 1, doi. 10.1002/macp.202000242
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Macromol. Chem. Phys. 3/2018.
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- Macromolecular Chemistry & Physics, 2018, v. 219, n. 3, p. 1, doi. 10.1002/macp.201870007
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Rotational Dynamics of a Probe in Rubbery Polymers Characterized by Time‐Resolved Fluorescence Anisotropy Measurement.
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- Macromolecular Chemistry & Physics, 2018, v. 219, n. 3, p. 1, doi. 10.1002/macp.201700329
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Design, Synthesis, and Photophysical Characterization of Biocompatible Thermally Activated Delayed Fluorescent Carbazole‐Coumarins for Sensing Applications.
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- Chemistry - A European Journal, 2024, v. 30, n. 55, p. 1, doi. 10.1002/chem.202401263
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A Photoredox Thiol‐yne Reaction for the Synthesis of Vinyl Sulfide‐Based Coumarins and its Effect on Fluorescence Properties.
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- Chemistry - A European Journal, 2024, v. 30, n. 44, p. 1, doi. 10.1002/chem.202401396
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Rational Design of Coumarin‐Based Hybridized Local and Charge‐Transfer Blue Emitters for Solution‐Processed Organic Light‐Emitting Diodes.
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- Chemistry - A European Journal, 2024, v. 30, n. 39, p. 1, doi. 10.1002/chem.202401078
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N‐Aryl‐DABCO Salts as an Unprecedented Sensing Platform for the Detection of Thiols and Selenols.
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- Chemistry - A European Journal, 2024, v. 30, n. 24, p. 1, doi. 10.1002/chem.202400229
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- Article
Development of Fluorescent Isocoumarin‐Fused Oxacyclononyne – 1,2,3‐Triazole Pairs.
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- Chemistry - A European Journal, 2023, v. 29, n. 47, p. 1, doi. 10.1002/chem.202300540
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Cover Feature: Phase‐Dependent Long Persistent Phosphorescence in Coumarin‐Phosphine‐Based Coinage Metal Complexes (Chem. Eur. J. 31/2023).
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- Chemistry - A European Journal, 2023, v. 29, n. 31, p. 1, doi. 10.1002/chem.202301396
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Coumarin C−H Functionalization by Mn(I) Carbonyls: Mechanistic Insight by Ultra‐Fast IR Spectroscopic Analysis.
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- Chemistry - A European Journal, 2023, v. 29, n. 25, p. 1, doi. 10.1002/chem.202203038
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Conjugating Coumarin with Tetraphenylethylene to Achieve Dual‐State Emission for Reversible Mechanofluorochromism and Live Cell Imaging.
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- Chemistry - A European Journal, 2023, v. 29, n. 24, p. 1, doi. 10.1002/chem.202203628
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Tuning Directed Photooxidation‐Induced Conversion of Pyrrole‐Based Styryl Coumarin Dual‐Color Photoconverters.
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- Chemistry - A European Journal, 2023, v. 29, n. 20, p. 1, doi. 10.1002/chem.202203933
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Front Cover: Tuning Directed Photooxidation‐Induced Conversion of Pyrrole‐Based Styryl Coumarin Dual‐Color Photoconverters (Chem. Eur. J. 20/2023).
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- Chemistry - A European Journal, 2023, v. 29, n. 20, p. 1, doi. 10.1002/chem.202300684
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Tuning Directed Photooxidation‐Induced Conversion of Pyrrole‐Based Styryl Coumarin Dual‐Color Photoconverters.
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- Chemistry - A European Journal, 2023, v. 29, n. 20, p. 1, doi. 10.1002/chem.202203933
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Metalloenzyme‐Mediated Thiol‐Yne Addition Towards Photoisomerizable Fluorescent Dyes.
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- Chemistry - A European Journal, 2022, v. 28, n. 62, p. 1, doi. 10.1002/chem.202202180
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Green‐Light Activatable BODIPY and Coumarin 5'‐Caps for Oligonucleotide Photocaging.
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- Chemistry - A European Journal, 2022, v. 28, n. 36, p. 1, doi. 10.1002/chem.202200477
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Strong Antibiotic Activity of the Myxocoumarin Scaffold in vitro and in vivo.
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- Chemistry - A European Journal, 2022, v. 28, n. 32, p. 1, doi. 10.1002/chem.202200394
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A Fluorogenic Inhibitor of the Mitochondrial Calcium Uniporter.
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- Angewandte Chemie, 2023, v. 135, n. 6, p. 1, doi. 10.1002/ange.202214920
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A Universal Photoactivatable Tag Attached to Fluorophores Enables Their Use for Single‐Molecule Imaging.
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- Angewandte Chemie, 2022, v. 134, n. 46, p. 1, doi. 10.1002/ange.202211767
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An Activity‐Based Ratiometric Fluorescent Probe for In Vivo Real‐Time Imaging of Hydrogen Molecules.
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- Angewandte Chemie, 2022, v. 134, n. 9, p. 1, doi. 10.1002/ange.202114594
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Bioorthogonal Ligation‐Activated Fluorogenic FRET Dyads.
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- Angewandte Chemie, 2022, v. 134, n. 6, p. 1, doi. 10.1002/ange.202111855
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- Article
Red‐Light‐Mediated Photoredox Catalysis Enables Self‐Reporting Nitric Oxide Release for Efficient Antibacterial Treatment.
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- Angewandte Chemie, 2021, v. 133, n. 37, p. 20615, doi. 10.1002/ange.202107155
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Coumarins by Direct Annulation: β‐Borylacrylates as Ambiphilic C<sub>3</sub>‐Synthons.
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- Angewandte Chemie, 2021, v. 133, n. 2, p. 695, doi. 10.1002/ange.202012099
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S‐Adenosyl Methionine Cofactor Modifications Enhance the Biocatalytic Repertoire of Small Molecule C‐Alkylation.
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- Angewandte Chemie, 2019, v. 131, n. 49, p. 17747, doi. 10.1002/ange.201908681
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Kinetic Resolution and Dynamic Kinetic Resolution of Chromene by Rhodium‐Catalyzed Asymmetric Hydroarylation.
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- Angewandte Chemie, 2019, v. 131, n. 16, p. 5397, doi. 10.1002/ange.201900721
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Porous silica as host for PEG-supported coumarin molecules.
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- Journal of Materials Science, 2013, v. 48, n. 19, p. 6797, doi. 10.1007/s10853-013-7484-5
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Synthesis of novel coumarin-terminated poly (p-phenylene vinylene)s for application in LEDs.
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- Journal of Materials Science, 2005, v. 40, n. 3, p. 601, doi. 10.1007/s10853-005-6295-8
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Phenotyping chlorogenic acids and coumarins in sweet potato [Ipomoea batatas (L.) Lam.] breeding lines for enhanced tolerance to periderm pathogens.
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- Euphytica, 2021, v. 217, n. 4, p. 1, doi. 10.1007/s10681-021-02808-w
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Fungitoxic effect of scopolin and related coumarins on Sclerotinia sclerotiorum. A way to overcome sunflower head rot.
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- Euphytica, 2006, v. 147, n. 3, p. 451, doi. 10.1007/s10681-005-9045-8
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Subdiffraction-limited chemical imaging of patterned phthalocyanine films using tip-enhanced near-field optical microscopy.
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- Journal of Raman Spectroscopy, 2016, v. 47, n. 11, p. 1287, doi. 10.1002/jrs.4968
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Bleeding incidence after oral surgery with continued oral anticoagulation.
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- Clinical Oral Investigations, 2012, v. 16, n. 5, p. 1371, doi. 10.1007/s00784-011-0649-1
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Extraction of C-PC from Arthrospira platensis: use of ultrasounds, organic solvents and deep eutectic solvents.
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- European Food Research & Technology, 2024, v. 250, n. 4, p. 1149, doi. 10.1007/s00217-023-04452-1
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Photo-protective effects of furocoumarins on terpenes in lime, lemon and bergamot essential oils upon UV light irradiation.
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- European Food Research & Technology, 2022, v. 248, n. 4, p. 1049, doi. 10.1007/s00217-021-03945-1
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A rapid UPLC-QqQ-MS/MS method for targeted screening and quantitative analysis of secondary metabolites in satsuma mandarin.
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- European Food Research & Technology, 2021, v. 247, n. 7, p. 1725, doi. 10.1007/s00217-021-03742-w
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Synthesis and Cytotoxicity Against Human Breast Carcinoma Cell Evaluation of Some New 3,4-Disubstituted Coumarin Derivatives.
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- Pharmaceutical Chemistry Journal, 2022, v. 55, n. 10, p. 1040, doi. 10.1007/s11094-021-02535-5
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Synthesis of Coumarins Coupled with Benzamides as Potent Antimicrobial Agents.
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- Pharmaceutical Chemistry Journal, 2020, v. 54, n. 6, p. 604, doi. 10.1007/s11094-020-02245-4
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Synthesis and Investigation of Antidiabetic Response of New Coumarin Derivatives Against Streptozotocin Induced Diabetes in Experimental Rats.
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- Pharmaceutical Chemistry Journal, 2020, v. 53, n. 12, p. 1122, doi. 10.1007/s11094-020-02134-w
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Synthesis and In Vivo Evaluation of New Coumarin Conjugates as Potential Indirect-Action Anticoagulants.
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- Pharmaceutical Chemistry Journal, 2019, v. 53, n. 5, p. 419, doi. 10.1007/s11094-019-02013-z
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Synthesis and Anticonvulsant Activity of N-Substituted 4-Amino-3-Nitrocoumarins.
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- Pharmaceutical Chemistry Journal, 2019, v. 53, n. 2, p. 118, doi. 10.1007/s11094-019-01964-7
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