On the public citation graph
Coumarin derivatives from Ainsliaea fragrans and their anticoagulant activity
0 signed · 133 inferred · view as graph
Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.
Is this your work? Sign in with ORCID and put your name on the
claims that are yours.
Reference health. See whether every reference in this work resolves to a
known work and none has been retracted — and get a dated CiteStamped
badge you can embed.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/anie.201107204openalex-snapshot
Enantiomeric Natural Products: Occurrence and Biogenesis
inferredcites →https://doi.org/10.1002/mrc.2294openalex-snapshot
Complete 1H and 13C data assignments of two new guaianolides isolated from Ainsliaea fragrans
inferredcites →https://doi.org/10.1002/pca.999openalex-snapshot
Preparative isolation and purification of dicaffeoylquinic acids from the Ainsliaea fragrans champ by high‐speed counter‐current chromatography
inferredcites →https://doi.org/10.1016/0031-9422(82)83061-6openalex-snapshot
Guaianolides from Ainsliaea fragrans
inferredcites →https://doi.org/10.1016/j.bmc.2009.08.031openalex-snapshot
Cytosporones, coumarins, and an alkaloid from the endophytic fungus Pestalotiopsis sp. isolated from the Chinese mangrove plant Rhizophora mucronata
inferredcites →https://doi.org/10.1016/j.bmc.2011.09.012openalex-snapshot
Effect of different C3-aryl substituents on the antioxidant activity of 4-hydroxycoumarin derivatives
inferredcites →https://doi.org/10.1016/j.fitote.2014.09.011openalex-snapshot
Comparative pharmacokinetics and tissue distribution study of mono-, and di-caffeoylquinic acids isomers of Ainsliaea fragrans Champ by a fast UHPLC–MS/MS method
inferredcites →https://doi.org/10.1016/j.phytochem.2013.09.005openalex-snapshot
Extensive phytochemical investigation of the polar constituents of Diospyros bipindensis Gürke traditionally used by Baka pygmies
inferredcites →https://doi.org/10.1016/j.tet.2007.09.006openalex-snapshot
Bargellini condensation of coumarins. Expeditious route to o-carboxyvinylphenoxyisobutyric acids and application to the synthesis of sesquiterpenes helianane, heliannuol A and heliannuol C
inferredcites →https://doi.org/10.1016/j.tet.2013.05.018openalex-snapshot
Synthesis of benzopyranopyrrolidines via 1,3-dipolar cycloaddition of nonstabilized azomethine ylides with 3-substituted coumarins
inferredcites →https://doi.org/10.1016/j.tetlet.2012.02.056openalex-snapshot
Coumarin derivatives from Pedilanthus tithymaloides as inhibitors of conidial germination in Magnaporthe oryzae
inferredcites →https://doi.org/10.1016/j.tetlet.2012.09.051openalex-snapshot
A simple and expedient synthesis of functionalized pyrido[2,3-c] coumarin derivatives using molecular iodine catalyzed three-component reaction
inferredcites →https://doi.org/10.1016/j.tetlet.2013.08.054openalex-snapshot
Induced production of novel prenyldepside and coumarins in endophytic fungi Pestalotiopsis acaciae
inferredcites →https://doi.org/10.1016/j.tetlet.2014.04.041openalex-snapshot
Palladium-catalyzed C3-selective mono-arylation of 4-hydroxycoumarin
inferredcites →https://doi.org/10.1016/j.tetlet.2014.10.078openalex-snapshot
An efficient synthesis of 4-substituted coumarin derivatives via a palladium-catalyzed Suzuki cross-coupling reaction
inferredcites →https://doi.org/10.1016/j.thromres.2015.01.017openalex-snapshot
Assessing the anticoagulant effect of dabigatran in children: An in vitro study
inferredcites →https://doi.org/10.1016/s0031-9422(00)81759-8openalex-snapshot
Chromones and coumarins from Skimmia laureola
inferredcites →https://doi.org/10.1016/s0031-9422(00)85512-0openalex-snapshot
Further 5-methyl coumarins and other constituents from the subtribe mutisiinae
inferredcites →https://doi.org/10.1016/s0031-9422(00)94370-xopenalex-snapshot
Neue 5-alkylcumarine und chromone aus Bothriocline laxa
inferredcites →https://doi.org/10.1016/s0040-4020(01)92011-3openalex-snapshot
Studies on the chemical constituents of rutaceous plants—XLI
inferredcites →https://doi.org/10.1016/s0040-4020(98)00762-5openalex-snapshot
Silver(I)/celite promoted oxidative cycloaddition of 4-hydroxycoumarin to olefins. A facile synthesis of dihydrofurocoumarins and furocoumarins
inferredcites →https://doi.org/10.1016/s0040-4039(00)85210-7openalex-snapshot
Synthesis of brachycoumarin and cyclobrachycoumarin
inferredcites →https://doi.org/10.1021/jm1013117openalex-snapshot
Flavonoids with an Oligopolysulfated Moiety: A New Class of Anticoagulant Agents
inferredcites →https://doi.org/10.1038/sj.tpj.6500417openalex-snapshot
Pharmacogenetics of warfarin: current status and future challenges
inferredcites →https://doi.org/10.1055/s-0030-1250176openalex-snapshot
Coumarin Derivatives fromGerbera saxatilis
inferredcites →https://doi.org/10.1080/10286020903014944openalex-snapshot
Two novel sesquiterpenoids fromAinsliaea fragransChamp.
inferredcites →https://doi.org/10.1248/cpb.38.2498openalex-snapshot
Isolation of two new coumarin glycosides from Notopterygium forbesii and evaluation of a Chinese crude drug, qiang-huo, the underground parts of N. incisum and N. forbesii, by high-performance liquid chromatography.
inferredcites →https://doi.org/10.1248/cpb.57.597openalex-snapshot
Sesquiterpenes from Ainsliaea fragrans and Their Inhibitory Activities against Cyclooxygenases-1 and 2
inferredcites →https://doi.org/10.1378/chest.119.1_suppl.8sopenalex-snapshot
Oral Anticoagulants: Mechanism of Action, Clinical Effectiveness, and Optimal Therapeutic Range
inferredcites →https://doi.org/10.2307/4587549openalex-snapshot
Control of Norway Rats with Residual Rodenticide Warfarin
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4144032openalex-extracted
Bioactive Constituents from Gerbera Piloselloides with Anti-Inflammatory and Antiproliferative Activities
inferred← citeshttps://doi.org/10.2139/ssrn.4791345openalex-extracted
Lc-Ms Coupled with Diagnostic Ion Strategy Facilitated Discovery of 5-Methylcoumarin Meroterpenoids from Gerbera Piloselloides
inferred← citeshttps://doi.org/10.1002/bio.3791openalex-snapshot
Quantum chemical computations and photophysical spectral features studies of two coumarin compounds
inferred← citeshttps://doi.org/10.1002/cbdv.202200315openalex-snapshot
Evaluation of Anti‐Alzheimer Activity of Synthetic Coumarins by Combination of in Vitro and in Silico Approaches
inferred← citeshttps://doi.org/10.1002/cbdv.202500251openalex-snapshot
Ainslials A–C: Three Underscribed Sesquiterpenes From Ainsliaea fragrans
inferred← citeshttps://doi.org/10.1002/cbdv.202503421openalex-snapshot
Secondary Metabolites of Ainsliaea fragrans and Their Cytotoxic Activity
inferred← citeshttps://doi.org/10.1002/jbt.23231openalex-snapshot
Synthesis, molecular docking, ADME study, and antimicrobial potency of piperazine based cinnamic acid bearing coumarin moieties as a DNA gyrase inhibitor
inferred← citeshttps://doi.org/10.1002/jhet.4912openalex-snapshot
Benzenediazonium Tetrafluoroborate‐Catalyzed Formal [3 + 3] Cyclization of 4‐Hydroxycoumarins With Propargylicalcohols
inferred← citeshttps://doi.org/10.1002/slct.201700687openalex-snapshot
Facile and Chemically Sustainable Catalyst‐Free Synthesis of Diverse 2‐Aryl‐4‐Alkyl/Aryl‐Pyrano[3,2‐ c ]chromen‐5(4 H )‐Ones by One‐Pot Multicomponent Reactions at Room Temperature
inferred← citeshttps://doi.org/10.1007/978-3-319-53112-0_8openalex-snapshot
Transformation of Natural Products into Synthetic Copolymers
inferred← citeshttps://doi.org/10.1007/978-3-319-59542-9_3openalex-snapshot
Progress in the Chemistry of Naturally Occurring Coumarins
inferred← citeshttps://doi.org/10.1007/s10600-023-04148-8openalex-snapshot
Furocoumarins from Ferula lehmannii
inferred← citeshttps://doi.org/10.1007/s10719-025-10180-3openalex-snapshot
Plant glycosides and glycosidases: classification, sources, and therapeutic insights in current medicine
inferred← citeshttps://doi.org/10.1007/s10895-020-02492-4openalex-snapshot
Synthesis of New Flexible Coumarin Dimers for Sodium and Potassium Differentiation
inferred← citeshttps://doi.org/10.1007/s11101-022-09828-xopenalex-snapshot
Taxonomic significance of coumarins in species from the subfamily Mutisioideae, Asteraceae
inferred← citeshttps://doi.org/10.1007/s11164-017-3210-2openalex-snapshot
Synthesis, docking and ADME prediction of novel 1,2,3-triazole-tethered coumarin derivatives as potential neuroprotective agents
inferred← citeshttps://doi.org/10.1007/s11244-022-01571-zopenalex-snapshot
RETRACTED ARTICLE: Recent Advances in the One-Pot Synthesis of Coumarin Derivatives from Different Starting Materials Using Nanoparticles: A Review
inferred← citeshttps://doi.org/10.1007/s12640-022-00632-1openalex-snapshot
Impact of Plant-Derived Compounds on Amyotrophic Lateral Sclerosis
inferred← citeshttps://doi.org/10.1007/s13204-021-01872-xopenalex-snapshot
Synthesis, characterization, and biomedical assessment of novel bisimidazole–coumarin conjugates
inferred← citeshttps://doi.org/10.1007/s44371-026-00693-7openalex-snapshot
Virtual screening of coumarin-linked naphthoquinone-fused pyrroles for antineoplastic activity and its DFT analysis
inferred← citeshttps://doi.org/10.1016/b978-0-12-820254-8.00033-6openalex-snapshot
The use of power ultrasound for green organic synthesis: Sonochemical organic reactions in aqueous media
inferred← citeshttps://doi.org/10.1016/b978-0-12-821006-2.00016-9openalex-snapshot
Biomedical applications of 4-hydroxycoumarin as a fungal metabolite and its derivatives
inferred← citeshttps://doi.org/10.1016/b978-0-12-821217-2.00003-1openalex-snapshot
Chemistry of natural and synthetic 2H-1-benzopyran-2-ones (coumarins)
inferred← citeshttps://doi.org/10.1016/b978-0-443-15650-2.00001-5openalex-snapshot
Development as antiinflammatory and anticoagulant agents
inferred← citeshttps://doi.org/10.1016/b978-0-443-15650-2.00005-2openalex-snapshot
Naturally occurring coumarins in the development of commercial drugs
inferred← citeshttps://doi.org/10.1016/j.apsb.2024.03.035openalex-snapshot
(+)/(−)-Gerbeloid A, a pair of unprecedented coumarin-based polycyclic meroterpenoid enantiomers from Gerbera piloselloides: Structural elucidation, semi-synthesis, and lipid-lowering activity
inferred← citeshttps://doi.org/10.1016/j.bcab.2019.101408openalex-snapshot
Stimulation of 6-benzylaminopurine and meta-topolin-induced in vitro shoot organogenesis and production of flavonoids of Amburana cearensis (Allemão) A.C. Smith)
inferred← citeshttps://doi.org/10.1016/j.bioorg.2022.105826openalex-snapshot
Coumarin-monoterpenes from Gerbera anandria (Linn.) Sch.-Bip and their neuroprotective activity
inferred← citeshttps://doi.org/10.1016/j.bse.2024.104949openalex-snapshot
Chemical constituents of Ainsliaea fragrans and their chemotaxonomic significance
inferred← citeshttps://doi.org/10.1016/j.cdc.2022.100862openalex-snapshot
Design, synthesis, molecular docking and antimicrobial and antimycobacterial activities of novel hybrid of coumarin-cinnamic acids
inferred← citeshttps://doi.org/10.1016/j.ejmech.2023.115699openalex-snapshot
Current development of 1,2,3-triazole derived potential antimalarial scaffolds: Structure- activity relationship (SAR) and bioactive compounds
inferred← citeshttps://doi.org/10.1016/j.ejmech.2025.117322openalex-snapshot
Antiproliferative activity of selenium-enriched coumarin derivatives on the SK-N-SH neuroblastoma cell line: Mechanistic insights
inferred← citeshttps://doi.org/10.1016/j.ejmech.2025.117426openalex-snapshot
A thiocoumarin based self-reporting sulfide prodrug strategy with a favorable safety profile
inferred← citeshttps://doi.org/10.1016/j.fitote.2021.104947openalex-snapshot
The antithrombotic activity of natural and synthetic coumarins
inferred← citeshttps://doi.org/10.1016/j.fitote.2022.105258openalex-snapshot
Bioactive constituents from Gerbera piloselloides with anti-inflammatory and antiproliferative activities
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2017.02.051openalex-snapshot
Bufadienolides from Kalanchoe daigremontiana as thrombin inhibitors— In vitro and in silico study
inferred← citeshttps://doi.org/10.1016/j.inoche.2025.115513openalex-snapshot
Engineering Nb2O5 embedded quinoline-linked COF as a high-performance catalyst for synthesis of tetrahydropyridines and α-aminobenzyl-4-hydroxycoumarins
inferred← citeshttps://doi.org/10.1016/j.lfs.2021.120210openalex-snapshot
Enigmatic role of exosomes in breast cancer progression and therapy
inferred← citeshttps://doi.org/10.1016/j.molstruc.2022.134414openalex-snapshot
Synthesis, anticancer evaluation, thermal and X-ray crystallographic analysis of 2-oxo-2H-chromen-7-yl 4-chlorobenzoate using a conductively heated sealed-vessel reactor
inferred← citeshttps://doi.org/10.1016/j.molstruc.2023.135493openalex-snapshot
Design and synthesis of novel 1,2,3-triazole linked hybrids: Molecular docking, MD simulation, and their antidiabetic efficacy as α-Amylase inhibitors
inferred← citeshttps://doi.org/10.1016/j.molstruc.2024.137601openalex-snapshot
6,7-Coumarin-heterocyclic hybrids: A comprehensive review of their natural sources, synthetic approaches, and bioactivity
inferred← citeshttps://doi.org/10.1016/j.molstruc.2024.140091openalex-snapshot
Fe3O4 magnetic nanoparticles (MNPs) as an efficient catalyst for allylic oxidation of chromenes to coumarins with TBHP
inferred← citeshttps://doi.org/10.1016/j.phrs.2020.105193openalex-snapshot
A pharmacological review of dicoumarol: An old natural anticoagulant agent
inferred← citeshttps://doi.org/10.1016/j.phymed.2024.155972openalex-snapshot
Coumarins as versatile therapeutic phytomolecules: A systematic review
inferred← citeshttps://doi.org/10.1016/j.phyplu.2025.100832openalex-snapshot
Linear furanocoumarins: Bridging natural wisdom and synthetic ingenuity in drug discovery
inferred← citeshttps://doi.org/10.1016/j.phytochem.2022.113346openalex-snapshot
1H-NMR-guided isolation of enantiomeric coumarin-monoterpenes with anti-inflammatory activity from Gerbera piloselloides
inferred← citeshttps://doi.org/10.1016/j.phytochem.2024.114296openalex-snapshot
LC–MS coupled with diagnostic ion strategy facilitated the discovery of 5-methylcoumarin meroterpenoids from Gerbera piloselloides
inferred← citeshttps://doi.org/10.1016/j.phytochem.2025.114415openalex-snapshot
Bonenncarpas A–K: Coumarin derivatives with anti-inflammatory activity from Boenninghausenia sessilicarpa
inferred← citeshttps://doi.org/10.1016/j.rechem.2025.102181openalex-snapshot
An overview of the synthesis of coumarins via Knoevenagel condensation and their biological properties
inferred← citeshttps://doi.org/10.1016/j.tet.2021.132001openalex-snapshot
Lactones: Classification, synthesis, biological activities, and industrial applications
inferred← citeshttps://doi.org/10.1021/acs.jpcb.5c06255openalex-snapshot
New Fluorescent Probes, Their Spectroscopic Properties, and an Iterative Analysis of Their Complexation with Cyclodextrins
inferred← citeshttps://doi.org/10.1039/9781788012782-00011openalex-snapshot
Catalyst-free Organic Reactions under Room Temperature Conditions
inferred← citeshttps://doi.org/10.1039/c6ra24332kopenalex-snapshot
Microbial transformation of methyl cyperenoate by Cunninghamella elegans AS 3.2028 and the antithrombotic activities of its metabolites
inferred← citeshttps://doi.org/10.1039/d2ob01206eopenalex-snapshot
Organocatalytic formal [3 + 3] cyclization of α-(6-indolyl) propargylic alcohols
inferred← citeshttps://doi.org/10.1039/d2ra03166copenalex-snapshot
Gerberdriasins A–F, six undescribed coumarin derivatives from Gerbera anandria (Linn) Sch-Bip and their protective effects on scopolamine-induced injury in PC12 cells
inferred← citeshttps://doi.org/10.1039/d4cc01953aopenalex-snapshot
An organocatalytic domino annulation approach via C(sp 2 )–OMe cleavage to unlock the synthesis of pyranochromenones enabled by HFIP
inferred← citeshttps://doi.org/10.1039/d4ob00509kopenalex-snapshot
l -Proline-catalysed synthesis of chromeno[2,3- b ]chromene from 4-hydroxy-2 H -chromene-2-thione and an anti-proliferative study
inferred← citeshttps://doi.org/10.1080/02678292.2017.1324644openalex-snapshot
Liquid-crystalline coumarin derivatives: contribution to the tailoring of metal-free sensitizers for solar cells
inferred← citeshttps://doi.org/10.1080/07328303.2019.1609018openalex-snapshot
Improved synthesis, X-ray structure, and antifungal activity of a sugar-psoralen conjugate: 4,4′-Dimethylxanthotoxol 2,3,4,6-tetra-O-Acetyl-β-D-glucoside
inferred← citeshttps://doi.org/10.1080/10406638.2021.1916543openalex-snapshot
Reactions and Antibacterial Activity of 6-Bromo-3-(2-Bromoacetyl)-2H-Chromen-2-One
inferred← citeshttps://doi.org/10.1080/10406638.2021.1998152openalex-snapshot
Synthesis of Coumarin Analogues Clubbed 1,3,4-Thiadiazine or Thiazole and Their Anticancer Activity
inferred← citeshttps://doi.org/10.1080/10826068.2022.2119573openalex-snapshot
The influence of UV light on the course of fluorescent enzyme assays
inferred← citeshttps://doi.org/10.1080/14786419.2019.1607336openalex-snapshot
Polyphenolics from Gymnocarpos decandrus Forssk roots and their biological activities
inferred← citeshttps://doi.org/10.1080/14786419.2025.2493190openalex-snapshot
A new coumarin from Tridax procumbens L. as potential anticancer, antibacterial, antioxidant agent and its molecular docking study
inferred← citeshttps://doi.org/10.1080/87559129.2026.2719721openalex-snapshot
Polyphenols as Therapeutic Candidates in the 21 st Century: From Chemical Discovery to Clinical Translation
inferred← citeshttps://doi.org/10.1111/1541-4337.12629openalex-snapshot
Evaluation of the status quo of polyphenols analysis: Part I—phytochemistry, bioactivity, interactions, and industrial uses
inferred← citeshttps://doi.org/10.1111/jth.15209openalex-snapshot
A novel vitamin K derived anticoagulant tolerant to genetic variations of vitamin K epoxide reductase
inferred← citeshttps://doi.org/10.1111/pbi.13742openalex-snapshot
Genome and systems biology of Melilotus albus provides insights into coumarins biosynthesis
inferred← citeshttps://doi.org/10.1149/1945-7111/abcf52openalex-snapshot
Electrochemistry and Reactivity Against Superoxide Anion Radicals of Hydroxycoumarins and Its Derivatives
inferred← citeshttps://doi.org/10.1155/2024/7377627openalex-snapshot
A Joint Analysis of Metabolomics, Network Pharmacology, and Molecular Docking Reveals the Efficacy Patterns in Various Medicinal Segments of Angelica sinensis (Oliv.) Diels Root
inferred← citeshttps://doi.org/10.1515/chem-2020-0128openalex-snapshot
Natural products isolated from Casimiroa
inferred← citeshttps://doi.org/10.18520/cs/v117/i11/1828-1841openalex-snapshot
Rice Husk SiO2 (NPs) Supported-BO3H3:A Highly Active, Solvent-Free and Recyclable Catalyst to Dihydropyrimidin-2(1H)ones- (Thiones) and Coumarin-3-Carboxylic Acid Synthesis
inferred← citeshttps://doi.org/10.21608/ejchem.2021.73699.3641openalex-snapshot
Synthesis, characterization, and anticoagulant activity of new functionalized biscoumarins
inferred← citeshttps://doi.org/10.2174/0109298673268452231108061008openalex-snapshot
Natural Phenolic Compounds with Antithrombotic and Antiplatelet Effects: A Drug-likeness Approach
inferred← citeshttps://doi.org/10.2174/0113852728371498250604114748openalex-snapshot
Triazole Hybrids and their Parasitic Inhibition Activities: A Mini Review
inferred← citeshttps://doi.org/10.2174/0118756298371734250611092234openalex-snapshot
Advances in the Determination of Chemical Composition and Pharmacological Properties of Ainsliaea spp.
inferred← citeshttps://doi.org/10.2174/1381612826666200515132218openalex-snapshot
Role of the Phytochemical Compounds like Modulators in Gut Microbiota and Oxidative Stress
inferred← citeshttps://doi.org/10.2174/1385272827666230206162235openalex-snapshot
One-Step, Low-Cost, Operator-Friendly, and Scalable Procedure to Synthetize Novel Tetrazolopyrimidinylbenzopyran-2-ones by Benign Protocol
inferred← citeshttps://doi.org/10.2174/1389557519666190925162536openalex-snapshot
Coumarin-based Scaffold as α-glucosidase Inhibitory Activity: Implication for the Development of Potent Antidiabetic Agents
inferred← citeshttps://doi.org/10.2174/1570179420666230427110019openalex-snapshot
Recent Advancement in Multicomponent Synthesis of Fused Coumarin Derivatives
inferred← citeshttps://doi.org/10.22146/ijc.65663openalex-snapshot
Novel Benzo[f]coumarin Derivatives as Probable Acetylcholinesterase Inhibitors: Synthesis, In Vitro, and In Silico Studies for Evaluation of Their Anti-AChE Activity
inferred← citeshttps://doi.org/10.22533/at.ed.813242230066openalex-snapshot
PHYTOCHEMICAL STUDY AND EVALUATION OF THE ANTIAGGREGATING EFFECT OF AQUEOUS AND ETHANOL EXTRACTS OF THE FUNGUS Amanita muscaria
inferred← citeshttps://doi.org/10.25077/jsfk.7.2.115-125.2020openalex-snapshot
Uji Aktivitas Antiplatelet, Antikoagulan, dan Trombolitik Alkaloid Total Daun Pepaya (Carica papaya L.) secara in Vitro
inferred← citeshttps://doi.org/10.3109/14756366.2015.1113173openalex-snapshot
Synthesis and carbonic anhydrase inhibitory properties of amino acid – coumarin/quinolinone conjugates incorporating glycine, alanine and phenylalanine moieties
inferred← citeshttps://doi.org/10.33102/mjosht.v7i1.145openalex-snapshot
Synthesis, Characterization, and Applications of Coumarin Derivatives: A Short Review
inferred← citeshttps://doi.org/10.3389/fchem.2018.00045openalex-snapshot
Natural Products Research in China From 2015 to 2016
inferred← citeshttps://doi.org/10.3390/ijerph20032046openalex-snapshot
Degradation Mechanisms of 4,7-Dihydroxycoumarin Derivatives in Advanced Oxidation Processes: Experimental and Kinetic DFT Study
inferred← citeshttps://doi.org/10.3390/ijms21134618openalex-snapshot
An Overview of Coumarin as a Versatile and Readily Accessible Scaffold with Broad-Ranging Biological Activities
inferred← citeshttps://doi.org/10.3390/molecules23010122openalex-snapshot
Novel 4-Methylumbelliferone Amide Derivatives: Synthesis, Characterization and Pesticidal Activities
inferred← citeshttps://doi.org/10.3390/molecules23030600openalex-snapshot
Novel Trifluoromethylcoumarinyl Urea Derivatives: Synthesis, Characterization, Fluorescence, and Bioactivity
inferred← citeshttps://doi.org/10.3390/molecules25061465openalex-snapshot
Antagonists of Vitamin K—Popular Coumarin Drugs and New Synthetic and Natural Coumarin Derivatives
inferred← citeshttps://doi.org/10.3390/molecules29235678openalex-snapshot
Cyclobrachycoumarin from Gerbera piloselloides Inhibits Colorectal Cancer In Vitro and In Vivo
inferred← citeshttps://doi.org/10.3390/polym13010056openalex-snapshot
Recent Advances in Functional Polymers Containing Coumarin Chromophores
inferred← citeshttps://doi.org/10.3390/w15061152openalex-snapshot
Natural Bioactive Phytocompounds to Reduce Toxicity in Common Carp Cyprinus carpio: A Challenge to Environmental Risk Assessment of Nanomaterials
inferred← citeshttps://doi.org/10.4155/fmc-2018-0375openalex-snapshot
Translational Role of Natural Coumarins and Their Derivatives As Anticancer Agents
inferred← citeshttps://doi.org/10.4274/tjps.galenos.2021.14603openalex-snapshot
In Vitro Activity of Some Medicinal Plants on Blood Coagulation
inferred← citeshttps://doi.org/10.47583/ijpsrr.2021.v68i01.001openalex-snapshot
Synthesis and Antibacterial Activities of Coumarins with an Acyl Amino Side Chain
inferred← citeshttps://doi.org/10.70675/7eb7646dz4f8dz44d2z9145z23e3e5812c98openalex-snapshot
Développement d’outils moléculaires et cellulaires pour générer des variétés de Pomelo « Star Ruby » ne produisant pas de Furocoumarines
Editorial review for independent work. ICSAC — the Institute for Complexity
Science and Advanced Computing — runs a structured editorial panel for researchers
publishing outside journals, and publishes on CiteStamp rails. Submission is free
and goes through ORCID: icsacinstitute.org/submit.