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Structure−Activity Relationship of New Anti-Hepatitis C Virus Agents: Heterobicycle−Coumarin Conjugates

https://doi.org/10.1021/jm801240d
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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/hep.1840360704openalex-snapshot
Course and outcome of hepatitis C
inferredcites →https://doi.org/10.1002/hep.21102openalex-snapshot
The non‐immunosuppressive cyclosporin DEBIO‐025 is a potent inhibitor of hepatitis C virus replication in vitro†
inferredcites →https://doi.org/10.1016/0960-894x(95)00001-aopenalex-snapshot
Acyl CoA:cholesterol acyltransferase (ACAT) inhibitors: ureas bearing heterocyclic groups bioisosteric for an imidazole
inferredcites →https://doi.org/10.1016/j.antiviral.2007.09.003openalex-snapshot
Synthesis of new benzimidazole–coumarin conjugates as anti-hepatitis C virus agents
inferredcites →https://doi.org/10.1016/j.bmc.2005.02.055openalex-snapshot
Syntheses of novel heterocycles as anticancer agents
inferredcites →https://doi.org/10.1016/j.bmc.2007.06.017openalex-snapshot
Synthesis and antitrichinellosis activity of some bis(benzimidazol-2-yl)amines
inferredcites →https://doi.org/10.1016/j.bmcl.2003.12.032openalex-snapshot
Non-nucleoside inhibitors of the hepatitis C virus NS5B polymerase: discovery of benzimidazole 5-carboxylic amide derivatives with low-nanomolar potency
inferredcites →https://doi.org/10.1016/j.bmcl.2004.06.069openalex-snapshot
Synthesis of C8-linked pyrrolo[2,1-c][1,4]benzodiazepine–benzimidazole conjugates with remarkable DNA-binding affinity
inferredcites →https://doi.org/10.1016/j.bmcl.2004.09.067openalex-snapshot
Antiviral compounds from traditional Chinese medicines Galla Chinese as inhibitors of HCV NS3 protease
inferredcites →https://doi.org/10.1016/j.bmcl.2006.01.032openalex-snapshot
Benzimidazole inhibitors of hepatitis C virus NS5B polymerase: Identification of 2-[(4-diarylmethoxy)phenyl]-benzimidazole
inferredcites →https://doi.org/10.1016/j.jhep.2004.11.025openalex-snapshot
Etanercept as an adjuvant to interferon and ribavirin in treatment-naive patients with chronic hepatitis C virus infection: a phase 2 randomized, double-blind, placebo-controlled study
inferredcites →https://doi.org/10.1016/s0001-706x(02)00217-6openalex-snapshot
Benzimidazole treatment of cystic echinococcosis
inferredcites →https://doi.org/10.1016/s0140-6736(01)06102-5openalex-snapshot
Peginterferon alfa-2b plus ribavirin compared with interferon alfa-2b plus ribavirin for initial treatment of chronic hepatitis C: a randomised trial
inferredcites →https://doi.org/10.1016/s0223-5234(01)01241-7openalex-snapshot
Synthesis and antitumour activity of trimethylsilylpropyl substituted benzimidazoles
inferredcites →https://doi.org/10.1016/s0223-5234(01)01313-7openalex-snapshot
Synthesis and anticancer and anti-HIV testing of some pyrazino[1,2-a]benzimidazole derivatives
inferredcites →https://doi.org/10.1016/s0223-5234(02)01421-6openalex-snapshot
Synthesis, antiprotozoal and anticancer activity of substituted 2-trifluoromethyl- and 2-pentafluoroethylbenzimidazoles
inferredcites →https://doi.org/10.1016/s0223-5234(03)00058-8openalex-snapshot
Synthesis, cytotoxic activity on MCF-7 cell line and mutagenic activity of platinum(II) complexes with 2-substituted benzimidazole ligands
inferredcites →https://doi.org/10.1016/s0960-894x(00)00429-7openalex-snapshot
Synthesis and antiproliferative activity of some benzimidazole-4,7-dione derivatives
inferredcites →https://doi.org/10.1021/jm00389a015openalex-snapshot
Synthesis, structure, and biological activity of certain 2-deoxy-.beta.-D-ribo-hexopyranosyl nucleosides and nucleotides
inferredcites →https://doi.org/10.1021/jm040134dopenalex-snapshot
Non-Nucleoside Benzimidazole-Based Allosteric Inhibitors of the Hepatitis C Virus NS5B Polymerase: Inhibition of Subgenomic Hepatitis C Virus RNA Replicons in Huh-7 Cells
inferredcites →https://doi.org/10.1021/jm040202wopenalex-snapshot
Novel C-17-Heteroaryl Steroidal CYP17 Inhibitors/Antiandrogens: Synthesis, in Vitro Biological Activity, Pharmacokinetics, and Antitumor Activity in the LAPC4 Human Prostate Cancer Xenograft Model
inferredcites →https://doi.org/10.1021/jm060269eopenalex-snapshot
Benzimidazole Derivatives Bearing Substituted Biphenyls as Hepatitis C Virus NS5B RNA-Dependent RNA Polymerase Inhibitors: Structure−Activity Relationship Studies and Identification of a Potent and Highly Selective Inhibitor JTK-109
inferredcites →https://doi.org/10.1021/ol035705vopenalex-snapshot
Efficient Route to 2-Deoxy β-O-Aryl- d -Glycosides via Direct Displacement of Glycosyl Iodides
inferredcites →https://doi.org/10.1039/b212303gopenalex-snapshot
Deoxygenation of carbohydrates by thiol-catalysed radical-chain redox rearrangement of the derived benzylidene acetals
inferredcites →https://doi.org/10.1055/s-2003-37655openalex-snapshot
Efficient and Chemoselective Access to 3-(Chloromethyl)coumarins via Direct Cyclisation of Unprotected Baylis-Hillman Adducts
inferredcites →https://doi.org/10.1056/nejm200107053450107openalex-snapshot
Hepatitis C Virus Infection
inferredcites →https://doi.org/10.1081/ncn-120023123openalex-snapshot
Resistance of Human Cytomegalovirus to D - and L -Ribosyl Benzimidazoles as a Tool to Identify Potential Targets for Antiviral Drugs
inferredcites →https://doi.org/10.1081/scc-120003150openalex-snapshot
SYNTHESIS OF 3′-AZIDO-2′,3′- DIDEOXY-4′-KETOHEXOPYRANOID ANALOGUES AS POSSIBLE ANTIVIRAL NUCLEOSIDES
inferredcites →https://doi.org/10.1093/nar/gkh160openalex-snapshot
Specific inhibitors of HCV polymerase identified using an NS5B with lower affinity for template/primer substrate
inferredcites →https://doi.org/10.1126/science.285.5424.110openalex-snapshot
Replication of Subgenomic Hepatitis C Virus RNAs in a Hepatoma Cell Line
inferredcites →https://doi.org/10.1128/jcm.40.12.4407-4412.2002openalex-snapshot
Laboratory Assays for Diagnosis and Management of Hepatitis C Virus Infection
inferredcites →https://doi.org/10.1177/095632020501600504openalex-snapshot
Synthesis and Biological Activity of 1H-benzotriazole and 1H-benzimidazole Analogues — Inhibitors of the NTPase/Helicase of HCV and of Some Related Flaviviridae
inferredcites →https://doi.org/10.2174/1389557053544047openalex-snapshot
Imidazole and Benzimidazole Derivatives as Chemotherapeutic Agents

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.4858080openalex-extracted
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inferred← citeshttps://doi.org/10.1002/adsc.200900287openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/adsc.201300990openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/adsc.201701140openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ajoc.201500235openalex-snapshot
Recent Advances in the Development of Pharmacologically Active Compounds that Contain a Benzoxazole Scaffold
inferred← citeshttps://doi.org/10.1002/ange.200903957openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.200903957openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/cbdv.201900462openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/cbdv.202200261openalex-snapshot
Daphnetin, a Coumarin in Genus Stellera Chamaejasme Linn: Chemistry, Bioactivity and Therapeutic Potential
inferred← citeshttps://doi.org/10.1002/chem.201100910openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ejoc.201600838openalex-snapshot
N‐Heterocyclic Carbene/Potassium Ion Cooperatively Catalyzed Phenylation Reactions of α,β‐Unsaturated Acylazoliums
inferred← citeshttps://doi.org/10.1002/ejoc.201701669openalex-snapshot
Solid Supported Nano Structured Cu‐Catalyst for Solvent/Ligand Free C 2 Amination of Azoles
inferred← citeshttps://doi.org/10.1002/ejoc.201900569openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ejoc.202001397openalex-snapshot
Unexpected Ring Opening During the Imination of Camphor‐Type Bicyclic Ketones
inferred← citeshttps://doi.org/10.1002/jccs.201700363openalex-snapshot
Recent Advances in the Synthesis of Biscoumarin Derivatives
inferred← citeshttps://doi.org/10.1002/jccs.201800444openalex-snapshot
Green synthesis of bis‐coumarin derivatives using Fe(SD)3as a catalyst and investigation of their biological activities
inferred← citeshttps://doi.org/10.1002/jccs.202000087openalex-snapshot
Heterogeneous SO3H @ Fe3O4 magnetic nanocatalyst as an efficient and reusable medium for the synthesis of 3,3′‐(arylmethylene)‐bis‐(4‐hydroxycoumarin), bis‐(indolyl)‐methane, and 1,8‐dioxo‐octahydroxanthene derivatives
inferred← citeshttps://doi.org/10.1002/jhet.2052openalex-snapshot
Copper‐catalyzed Cyclization of 3‐Acylcoumarin Hydrazone using Air as the Oxidant: Efficient Synthesis of Pyrazole‐Fused Coumarin Derivatives
inferred← citeshttps://doi.org/10.1002/jhet.2104openalex-snapshot
Improved and Efficient Synthesis of Chromeno[4,3‐d]pyrazolo [3,4‐b]pyridin‐6(3H)‐ones and Their Fluorescence Properties
inferred← citeshttps://doi.org/10.1002/jhet.2255openalex-snapshot
An Efficient Synthesis of Chromeno[4,3-d]isoxazolo[5,4-b]pyridin-6-one Derivatives
inferred← citeshttps://doi.org/10.1002/jhet.298openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/jhet.4634openalex-snapshot
Catalyst‐free access to substituted pyrano[4,3‐ b ]pyrrol‐4( 1 H )‐one derivatives through domino reaction in water
inferred← citeshttps://doi.org/10.1002/open.202400319openalex-snapshot
A Facile Synthesis of 3‐Substituted Coumarins and Investigation of Their 3CLpro Inhibition Activity Against SARS‐CoV‐2
inferred← citeshttps://doi.org/10.1002/slct.201903632openalex-snapshot
An Insight View on Synthetic Protocol, Mechanistic and Biological Aspects of Biscoumarin Derivatives
inferred← citeshttps://doi.org/10.1002/slct.202100928openalex-snapshot
Synthesis and Molecular Docking Studies of Potent Urease Inhibitors Based on Benzoxazole Scaffold
inferred← citeshttps://doi.org/10.1002/slct.202101853openalex-snapshot
Design and Synthesis of Bioinspired Benzocoumarin‐Chalcones Chimeras as Potential Anti‐Breast Cancer Agents
inferred← citeshttps://doi.org/10.1002/slct.202300126openalex-snapshot
I 2 /DMSO mediated Cascade cyclization reaction of amino coumarins with aryl methyl ketones: Access to Dicoumarino‐fused [1,5]‐diazocine and pyrrolo‐coumarin scaffolds
inferred← citeshttps://doi.org/10.1002/slct.202302786openalex-snapshot
SO 3 H‐Functionalized Carbon Materials: A Versatile and sustainable heterogeneous Catalyst for Diverse Organic Transformations
inferred← citeshttps://doi.org/10.1002/slct.202403778openalex-snapshot
Computational Insights into the Electronic Structure of 3‐Phenyl Coumarins
inferred← citeshttps://doi.org/10.1007/s10870-010-9917-1openalex-snapshot
Crystal Structure Studies of Two Regioisomers of Bromo-4-Aryloxymethylcoumarins
inferred← citeshttps://doi.org/10.1007/s10895-023-03345-6openalex-snapshot
Synthesis and Fluorescence Properties of Imidazopyridine-Linked Coumarins via Tandem C(sp2)–H Functionalization/Decarboxylation Reaction
inferred← citeshttps://doi.org/10.1007/s11030-022-10393-wopenalex-snapshot
Synthesis of novel pyrano[2,3-f]chromene-dione derivatives using phosphoric acid-functionalized silica-coated Fe3O4 nanoparticles as a new reusable solid acid nanocatalyst
inferred← citeshttps://doi.org/10.1007/s11164-011-0423-7openalex-snapshot
Synthesis, characterization, and biological evaluation of new N-glycosides derived from O-pivaloylated β-d-glucopyranosylamine
inferred← citeshttps://doi.org/10.1007/s11164-018-3490-1openalex-snapshot
Synthesis and biological evaluation of novel triazole-biscoumarin conjugates as potential antitubercular and anti-oxidant agents
inferred← citeshttps://doi.org/10.1007/s11164-019-03913-1openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s11164-025-05827-7openalex-snapshot
General and efficient one-pot synthesis of chromeno[4,3-b] chromenes and tetrahydrodipyrazolopyridines using reproducible deep eutectic solvent: a green protocol at mild temperature
inferred← citeshttps://doi.org/10.1007/s11224-019-01473-zopenalex-snapshot
Kamonolol acetate from Ferula pseudalliacea as AChE inhibitor: in vitro and in silico studies
inferred← citeshttps://doi.org/10.1007/s11696-024-03498-zopenalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s11696-026-04690-zopenalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s12039-019-1647-0openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s12633-023-02799-4openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s40242-013-3107-6openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s40242-017-6472-8openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-12-803797-3.00017-5openalex-snapshot
References
inferred← citeshttps://doi.org/10.1016/b978-0-323-85386-6.00004-4openalex-snapshot
Benzoxazole
inferred← citeshttps://doi.org/10.1016/b978-0-443-15650-2.00009-xopenalex-snapshot
Role of coumarins in different infectious diseases
inferred← citeshttps://doi.org/10.1016/b978-0-443-15650-2.00011-8openalex-snapshot
Multitargeted scaffold in medicinal chemistry: Potential anticancer agents
inferred← citeshttps://doi.org/10.1016/j.antiviral.2011.03.143openalex-snapshot
Coumarins Hybridized with Heterocycles or Ribonucleosides for Eradication of Hepatitis C Virus
inferred← citeshttps://doi.org/10.1016/j.antiviral.2015.03.013openalex-snapshot
Benzouracil–coumarin–arene conjugates as inhibiting agents for chikungunya virus
inferred← citeshttps://doi.org/10.1016/j.antiviral.2021.105192openalex-snapshot
Potential application of antiviral coumarin in aquaculture against IHNV infection by reducing viral adhesion to the epithelial cell surface
inferred← citeshttps://doi.org/10.1016/j.apsusc.2023.158224openalex-snapshot
Aminocoumarin derivatives grafted on graphene oxide - new antimicrobial agents to combat the resistance of Mycobacterium tuberculosis and ESKAPE pathogens
inferred← citeshttps://doi.org/10.1016/j.aquaculture.2020.735412openalex-snapshot
Rhabdoviral clearance effect of a phenylpropanoid medicine against spring viremia of carp virus infection in vitro and in vivo
inferred← citeshttps://doi.org/10.1016/j.aquaculture.2021.736999openalex-snapshot
Synthesis and application of a potential therapeutic coumarin derivative against IHNV in aquaculture
inferred← citeshttps://doi.org/10.1016/j.arabjc.2014.07.006openalex-snapshot
Overview on the recently developed coumarinyl heterocycles as useful therapeutic agents
inferred← citeshttps://doi.org/10.1016/j.bioorg.2025.108845openalex-snapshot
Synthesis and antiviral activity of new 4-substituted Oxycoumarins against SARS and HSV-2 viruses: Mechanistic and molecular modeling study
inferred← citeshttps://doi.org/10.1016/j.biopha.2025.118252openalex-snapshot
Targeting SARS-CoV-2 RNA-dependent RNA polymerase with the coumarin derivative BPR2-D2: Evidence from cell-based and enzymatic studies
inferred← citeshttps://doi.org/10.1016/j.bmc.2010.03.024openalex-snapshot
Allosteric inhibitors of hepatitis C virus NS5B polymerase thumb domain site II: Structure-based design and synthesis of new templates
inferred← citeshttps://doi.org/10.1016/j.bmc.2013.02.017openalex-snapshot
A comprehensive review on synthesis and designing aspects of coumarin derivatives as monoamine oxidase inhibitors for depression and Alzheimer’s disease
inferred← citeshttps://doi.org/10.1016/j.bmc.2013.04.015openalex-snapshot
Remarkable antioxidant properties of a series of hydroxy-3-arylcoumarins
inferred← citeshttps://doi.org/10.1016/j.bmc.2014.05.032openalex-snapshot
Coumarin hybrids as novel therapeutic agents
inferred← citeshttps://doi.org/10.1016/j.bmc.2014.10.008openalex-snapshot
Structural modifications of coumarin derivatives: Determination of antioxidant and lipoxygenase (LOX) inhibitory activity
inferred← citeshttps://doi.org/10.1016/j.bmcl.2011.05.074openalex-snapshot
MAO inhibitory activity modulation: 3-Phenylcoumarins versus 3-benzoylcoumarins
inferred← citeshttps://doi.org/10.1016/j.bmcl.2011.11.020openalex-snapshot
Hydroxycoumarins as selective MAO-B inhibitors
inferred← citeshttps://doi.org/10.1016/j.bmcl.2012.12.071openalex-snapshot
Synthesis of new conjugated coumarin–benzimidazole hybrids and their anticancer activity
inferred← citeshttps://doi.org/10.1016/j.bmcl.2013.12.095openalex-snapshot
Synthesis and biological evaluation of 4-(1,2,3-triazol-1-yl)coumarin derivatives as potential antitumor agents
inferred← citeshttps://doi.org/10.1016/j.bmcl.2014.08.037openalex-snapshot
Synthesis and evaluation of new 3-phenylcoumarin derivatives as potential antidepressant agents
inferred← citeshttps://doi.org/10.1016/j.bmcl.2019.05.019openalex-snapshot
Synthesis and antiviral activity of coumarin derivatives against infectious hematopoietic necrosis virus
inferred← citeshttps://doi.org/10.1016/j.bmcl.2025.130444openalex-snapshot
Coumarin–benzimidazole hybrids: Design, synthesis and identification of potential anticancer agents
inferred← citeshttps://doi.org/10.1016/j.carres.2023.108857openalex-snapshot
Recent advances in synthesis of sugar and nucleoside coumarin conjugates and their biological impact
inferred← citeshttps://doi.org/10.1016/j.cbi.2016.05.001openalex-snapshot
Coumarins as cholinesterase inhibitors: A review
inferred← citeshttps://doi.org/10.1016/j.ejmech.2013.02.008openalex-snapshot
Coumarins hinged directly on benzimidazoles and their ribofuranosides to inhibit hepatitis C virus
inferred← citeshttps://doi.org/10.1016/j.ejmech.2014.03.018openalex-snapshot
Rational approaches, design strategies, structure activity relationship and mechanistic insights for anticancer hybrids
inferred← citeshttps://doi.org/10.1016/j.ejmech.2015.06.017openalex-snapshot
Recent progress in the drug development of coumarin derivatives as potent antituberculosis agents
inferred← citeshttps://doi.org/10.1016/j.ejmech.2016.07.056openalex-snapshot
Therapeutic potential of coumarins as antiviral agents
inferred← citeshttps://doi.org/10.1016/j.ejmech.2016.09.021openalex-snapshot
Synthesis, characterization and molecular docking studies of substituted 4-coumarinylpyrano[2,3-c]pyrazole derivatives as potent antibacterial and anti-inflammatory agents
inferred← citeshttps://doi.org/10.1016/j.ejmech.2017.11.100openalex-snapshot
Synthesis and biological evaluation of coumarin derivatives containing imidazole skeleton as potential antibacterial agents
inferred← citeshttps://doi.org/10.1016/j.ejmech.2019.01.037openalex-snapshot
Chikungunya virus inhibition by synthetic coumarin–guanosine conjugates
inferred← citeshttps://doi.org/10.1016/j.ejmech.2019.01.070openalex-snapshot
Excellent antitumor and antimetastatic activities based on novel coumarin/pyrazole oxime hybrids
inferred← citeshttps://doi.org/10.1016/j.ejmech.2019.02.048openalex-snapshot
New 4-phenylcoumarin derivatives as potent 3C protease inhibitors: Design, synthesis, anti-HAV effect and molecular modeling
inferred← citeshttps://doi.org/10.1016/j.ejmech.2021.113739openalex-snapshot
Synthesis and biological evaluation of novel coumarin derivatives in rhabdoviral clearance
inferred← citeshttps://doi.org/10.1016/j.ejmech.2021.113921openalex-snapshot
Coumarin–benzimidazole hybrids: A review of developments in medicinal chemistry
inferred← citeshttps://doi.org/10.1016/j.ejmech.2022.114164openalex-snapshot
Synthesis and antiviral activities of quinazolinamine–coumarin conjugates toward chikungunya and hepatitis C viruses
inferred← citeshttps://doi.org/10.1016/j.ejmech.2024.116487openalex-snapshot
Design, synthesis and bioactivity evaluation of 4-hydroxycoumarin derivatives as potential anti-inflammatory agents against acute lung injury and colitis
inferred← citeshttps://doi.org/10.1016/j.fitote.2014.10.011openalex-snapshot
Inhibition of hepatitis C virus replication by chalepin and pseudane IX isolated from Ruta angustifolia leaves
inferred← citeshttps://doi.org/10.1016/j.foodchem.2012.07.055openalex-snapshot
Biological evaluation of coumarin derivatives as mushroom tyrosinase inhibitors
inferred← citeshttps://doi.org/10.1016/j.fsi.2025.110633openalex-snapshot
Emodin enhances host antiviral immunity against Micropterus salmoides rhabdovirus by activating RLR signaling in largemouth bass
inferred← citeshttps://doi.org/10.1016/j.gendis.2021.03.007openalex-snapshot
Pharmacological perspectives and molecular mechanisms of coumarin derivatives against virus disease
inferred← citeshttps://doi.org/10.1016/j.heliyon.2020.e03217openalex-snapshot
Coumarin: An emerging antiviral agent
inferred← citeshttps://doi.org/10.1016/j.jfluchem.2016.01.002openalex-snapshot
Simultaneous exploration of TBAF·3H 2 O as a base as well as a solvating agent for the palladium catalyzed Suzuki cross-coupling of 4-methyl-7-nonafluorobutylsulfonyloxy coumarins under microwave irradiation
inferred← citeshttps://doi.org/10.1016/j.jinorgbio.2015.10.007openalex-snapshot
Spectroscopic studies, DFT calculations, and cytotoxic activity of novel silver(I) complexes of hydroxy ortho-substituted-nitro-2H-chromen-2-one ligands and a phenanthroline adduct
inferred← citeshttps://doi.org/10.1016/j.jphotochem.2024.115494openalex-snapshot
A new dual nickel/ferrocenyl-chalcone as photoredox catalyst along with DFT studies for the three-component domino performance
inferred← citeshttps://doi.org/10.1016/j.mencom.2020.11.024openalex-snapshot
Synthesis and antibacterial evaluation of novel mono- and bis(2H-chromen-2-imine) hybrids linked to heteroarene units
inferred← citeshttps://doi.org/10.1016/j.molstruc.2019.127047openalex-snapshot
Synthesis, in vitro cytotoxicity activity against the human cervix carcinoma cell line and in silico computational predictions of new 4-arylamino-3-nitrocoumarin analogues
inferred← citeshttps://doi.org/10.1016/j.molstruc.2019.127577openalex-snapshot
Synthesis, structure, cytotoxic and antioxidant properties of 6-ethoxy-4-methylcoumarin
inferred← citeshttps://doi.org/10.1016/j.molstruc.2021.131476openalex-snapshot
Potential bacterial biofilm, MRSA, and DHFR inhibitors based on new morpholine-linked chromene-thiazole hybrids: One-pot synthesis and in silico study
inferred← citeshttps://doi.org/10.1016/j.molstruc.2022.132840openalex-snapshot
N-Tosylindole-coumarin with high fluorescence quantum yield and their potential applications
inferred← citeshttps://doi.org/10.1016/j.molstruc.2023.136229openalex-snapshot
Synthesis and biological evaluation of coumarin appended thiazole hybrid heterocycles: Antibacterial and antifungal study
inferred← citeshttps://doi.org/10.1016/j.molstruc.2023.137197openalex-snapshot
Coumarin–1,2,4-triazole hybrids: Recent advances in synthesis and medicinal applications
inferred← citeshttps://doi.org/10.1016/j.molstruc.2024.140111openalex-snapshot
Synthesis and evaluation of the anti-TB activity of novel 7-(2-(4-substituted-phenyl)-4,5-diphenyl-1H-imidazol-1-yl)-4-methyl-2H-chromen-2-one derivatives and their DFT studies for NLO application
inferred← citeshttps://doi.org/10.1016/j.molstruc.2025.144911openalex-snapshot
Recent advances of phenylsulfonylfuroxan derivatives and their structure-activity relationships
inferred← citeshttps://doi.org/10.1016/j.phytol.2024.01.010openalex-snapshot
Coumarin hybrids for targeted therapies: A promising approach for potential drug candidates
inferred← citeshttps://doi.org/10.1016/j.rechem.2025.102679openalex-snapshot
Synthesis, characterization, comparative study, DFT analysis, ADMET prediction and molecular docking study of Thiophen-2-yl and 4-pyridinyl derivatives of bis (4-hydroxy-2H-chromen-2-one)
inferred← citeshttps://doi.org/10.1016/j.rechem.2026.103287openalex-snapshot
Green synthesis of bis-coumarins using magnetically separable catalysts: In-silico, MTT assay, apoptosis and cell cycle studies against breast Cancer
inferred← citeshttps://doi.org/10.1016/j.tet.2016.01.023openalex-snapshot
Synthesis of novel imidazo[1,2-a]pyridine-4-hydroxy-2H-coumarins by Groebke–Blackburn–Bienaymé multicomponent reaction as potential NS5B inhibitors
inferred← citeshttps://doi.org/10.1016/j.tet.2024.134025openalex-snapshot
PEG-mediated synthesis of naphthoquinone/coumarin fused dihydropyridine derivatives
inferred← citeshttps://doi.org/10.1016/j.tetlet.2009.12.089openalex-snapshot
Synthesis of biologically potent new 3-(heteroaryl)aminocoumarin derivatives via Buchwald–Hartwig C–N coupling
inferred← citeshttps://doi.org/10.1016/j.tetlet.2010.11.028openalex-snapshot
4-Chloro-3-(trifluoroacetyl)coumarin as a novel building block for the synthesis of 7-(trifluoromethyl)-6H-chromeno[4,3-b]quinolin-6-ones
inferred← citeshttps://doi.org/10.1016/j.tetlet.2012.02.077openalex-snapshot
An efficient green protocol for the synthesis of coumarin fused highly decorated indenodihydropyridyl and dihydropyridyl derivatives
inferred← citeshttps://doi.org/10.1016/j.tetlet.2012.10.096openalex-snapshot
Design and synthesis of condensed thienocoumarins by Suzuki–Miyaura reaction/lactonization tandem protocol
inferred← citeshttps://doi.org/10.1016/j.tetlet.2012.12.079openalex-snapshot
Dual role of the polymer supported catalyst PEG-OSO3H in aqueous reaction medium: synthesis of highly substituted structurally diversified coumarin and uracil fused spirooxindoles
inferred← citeshttps://doi.org/10.1016/j.tetlet.2013.04.001openalex-snapshot
Fe(DS)3, an efficient Lewis acid-surfactant-combined catalyst (LASC) for the one pot synthesis of chromeno[4,3-b]chromene derivatives by assembling the basic building blocks
inferred← citeshttps://doi.org/10.1016/j.tetlet.2013.08.030openalex-snapshot
A convenient approach to the design and synthesis of indolo[3,2-c]coumarins via the microwave-assisted Cadogan reaction
inferred← citeshttps://doi.org/10.1016/j.tetlet.2014.02.094openalex-snapshot
A rapid approach for the copper, amine, and ligand-free Sonogashira coupling of 4-methyl-7-nonafluorobutylsulfonyloxy coumarins under microwave irradiation
inferred← citeshttps://doi.org/10.1016/j.tetlet.2015.09.111openalex-snapshot
New approach to synthesis of 4-arylcoumarin derivatives
inferred← citeshttps://doi.org/10.1016/j.tetlet.2016.06.061openalex-snapshot
Regioselective transition metal-free acylation of coumarins via cross-dehydrogenative coupling reaction of coumarins and aldehydes
inferred← citeshttps://doi.org/10.1016/j.tetlet.2017.01.062openalex-snapshot
New method for the synthesis of chromeno[4,3-b]chromene derivatives via multicomponent reaction promoted by niobium pentachloride
inferred← citeshttps://doi.org/10.1016/j.tetlet.2021.152904openalex-snapshot
Synthesis of novel tetracyclic coumarin-fused furo-pyridone scaffolds via sequential N-arylation and intramolecular amidation reactions
inferred← citeshttps://doi.org/10.1016/j.virusres.2021.198387openalex-snapshot
A novel antiviral coumarin derivative as a potential agent against WSSV infection in shrimp seedling culture
inferred← citeshttps://doi.org/10.1016/s1872-2067(14)60061-9openalex-snapshot
Poly(4-vinylpyridinium) perchlorate as an efficient and recyclable catalyst for the synthesis of biscoumarins and bisindoles
inferred← citeshttps://doi.org/10.1021/acs.jchemed.0c01308openalex-snapshot
Bis-4-hydroxycoumarin Synthesis: A Simple Laboratory Experiment for Undergraduate Students
inferred← citeshttps://doi.org/10.1021/acs.joc.2c00958openalex-snapshot
Access to π-Extended Heterocycles Containing Pyrrolo-Coumarin Cores Involving −COCH3 as a Traceless Directing Group and Materializing Two Successive sp2C–H/sp3N–H and sp2C–H/sp2N–H Activations
inferred← citeshttps://doi.org/10.1021/acs.joc.3c01742openalex-snapshot
Synthesis, Structural, and Optical Properties of Azuleno[1,2-c]pyran-1-ones: Bronsted Acid-Mediated Cyclization of 2-Azulenylalkynes
inferred← citeshttps://doi.org/10.1021/acs.orglett.3c01189openalex-snapshot
Asymmetric Organocatalysis in the Remote (3 + 2)-Cycloaddition to 4-(Alk-1-en-1-yl)-3-cyanocoumarins
inferred← citeshttps://doi.org/10.1021/acsomega.8b01993openalex-snapshot
Metal-Free Construction of Fused Pyrimidines via Consecutive C–C and C–N Bond Formation in Water
inferred← citeshttps://doi.org/10.1021/acssuschemeng.7b04048openalex-snapshot
Ionic Liquid-Coated Carbon Nanotubes as Efficient Metal-Free Catalysts for the Synthesis of Chromene Derivatives
inferred← citeshttps://doi.org/10.1021/acssuschemeng.9b05682openalex-snapshot
Catalyst-Free One-Pot Three-Component Synthesis of 4-Hydroxy-3-pyrazolylcoumarins in Ethanol at Room Temperature: Enolisable Aroylhydrazones as Efficient Ambident Nucleophile
inferred← citeshttps://doi.org/10.1021/jacs.7b01983openalex-snapshot
AgPd Nanoparticles Deposited on WO2.72 Nanorods as an Efficient Catalyst for One-Pot Conversion of Nitrophenol/Nitroacetophenone into Benzoxazole/Quinazoline
inferred← citeshttps://doi.org/10.1021/jm101337vopenalex-snapshot
Coumarin−Purine Ribofuranoside Conjugates as New Agents against Hepatitis C Virus
inferred← citeshttps://doi.org/10.1021/jm200716yopenalex-snapshot
Synthesis and Study of a Series of 3-Arylcoumarins as Potent and Selective Monoamine Oxidase B Inhibitors
inferred← citeshttps://doi.org/10.1038/nprot.2010.132openalex-snapshot
A rapid and efficient route to benzazole heterocycles
inferred← citeshttps://doi.org/10.1038/srep36225openalex-snapshot
Na@SiO2-Mediated Addition of Organohalides to Carbonyl Compounds for the Formation of Alcohols and Epoxides
inferred← citeshttps://doi.org/10.1039/b925424bopenalex-snapshot
Aminocatalytic asymmetric inverse-electron-demand aza-Diels–Alder reaction of N-Ts-1-aza-1,3-butadienes based on coumarin cores
inferred← citeshttps://doi.org/10.1039/c2cy20117hopenalex-snapshot
A new application of polymer supported, homogeneous and reusable catalyst PEG–SO3H in the synthesis of coumarin and uracil fused pyrrole derivatives
inferred← citeshttps://doi.org/10.1039/c2ob25962aopenalex-snapshot
Palladium-catalyzed, pyrrolidine-mediated arylmethylation of ketones and aldehydes with coumarinyl(methyl) acetates
inferred← citeshttps://doi.org/10.1039/c2ob26860dopenalex-snapshot
Novel anilinocoumarin derivatives as agents against hepatitis C virus by the induction of IFN-mediated antiviral responses
inferred← citeshttps://doi.org/10.1039/c2sc20248dopenalex-snapshot
A concise, efficient synthesis of sugar-based benzothiazoles through chemoselective intramolecular C–S coupling
inferred← citeshttps://doi.org/10.1039/c3ra23254aopenalex-snapshot
Facile synthesis of pyridopyrimidine and coumarin fused pyridine libraries over a Lewis base-surfactant-combined catalyst TEOA in aqueous medium
inferred← citeshttps://doi.org/10.1039/c3ra40571kopenalex-snapshot
Three-component synthesis of a polysubstituted pyrrole core containing heterocyclic scaffolds over magnetically separable nanocrystalline copper ferrite
inferred← citeshttps://doi.org/10.1039/c3ra44053bopenalex-snapshot
Sulfonated rice husk ash (RHA-SO3H) as a highly efficient and reusable catalyst for the synthesis of some bis-heterocyclic compounds
inferred← citeshttps://doi.org/10.1039/c3ra46428hopenalex-snapshot
Regioselective synthesis of 9,10-dihydro-6H-chromeno[4,3-d]imidazo-[1,2-a]pyridin-6-one derivatives
inferred← citeshttps://doi.org/10.1039/c4ob00618fopenalex-snapshot
Synthesis of functionalized chromones through sequential reactions in aqueous media
inferred← citeshttps://doi.org/10.1039/c4ra01720jopenalex-snapshot
A rapid and modified approach for C-7 amination and amidation of 4-methyl-7-nonafluorobutylsulfonyloxy coumarins under microwave irradiation
inferred← citeshttps://doi.org/10.1039/c4ra12618aopenalex-snapshot
Synthesis of indeno and acenaphtho cores containing dihydroxy indolone, pyrrole, coumarin and uracil fused heterocyclic motifs under sustainable conditions exploring the catalytic role of the SnO 2 quantum dot
inferred← citeshttps://doi.org/10.1039/c5ra06532aopenalex-snapshot
Sulfonated polyethylene glycol (PEG-OSO 3 H) as a polymer supported biodegradable and recyclable catalyst in green organic synthesis: recent advances
inferred← citeshttps://doi.org/10.1039/c6nj03763aopenalex-snapshot
Zwitterionic liquid (ZIL) coated CuO as an efficient catalyst for the green synthesis of bis-coumarin derivatives via one-pot multi-component reactions using mechanochemistry
inferred← citeshttps://doi.org/10.1039/c6ra04893eopenalex-snapshot
A clean synthesis of bis(indolyl)methane and biscoumarin derivatives using P 4 VPy–CuO nanoparticles as a new, efficient and heterogeneous polymeric catalyst
inferred← citeshttps://doi.org/10.1039/c6ra06979gopenalex-snapshot
Facile and eco-friendly synthesis of chromeno[4,3-b]pyrrol-4(1H)-one derivatives applying magnetically recoverable nano crystalline CuFe 2 O 4 involving a domino three-component reaction in aqueous media
inferred← citeshttps://doi.org/10.1039/c6ra08111hopenalex-snapshot
Eco-friendly grinding synthesis of a double-layered nanomaterial and the correlation between its basicity, calcination and catalytic activity in the green synthesis of novel fused pyrimidines
inferred← citeshttps://doi.org/10.1039/c6ra17814fopenalex-snapshot
Two-step three-component process for one-pot synthesis of 8-alkylmercaptocaffeine derivatives
inferred← citeshttps://doi.org/10.1039/c8ra07517dopenalex-snapshot
An efficient, mild and metal free l -proline catalyzed construction of fused pyrimidines under microwave conditions in water
inferred← citeshttps://doi.org/10.1039/d1me00113bopenalex-snapshot
Design, synthesis, structural analysis and quantum chemical insight into the molecular structure of coumarin derivatives
inferred← citeshttps://doi.org/10.1039/d1qo01602dopenalex-snapshot
Visible light photocatalysis in the synthesis of pharmaceutically relevant heterocyclic scaffolds
inferred← citeshttps://doi.org/10.1039/d1ra08763kopenalex-snapshot
Diverse and efficient catalytic applications of new cockscomb flower-like Fe 3 O 4 @SiO 2 @KCC-1@MPTMS@Cu II mesoporous nanocomposite in the environmentally benign reduction and reductive acetylation of nitroarenes and one-pot synthesis of some coumarin compounds
inferred← citeshttps://doi.org/10.1039/d2ra07134gopenalex-snapshot
Synthesis, spectroscopic, SC-XRD/DFT and non-linear optical (NLO) properties of chromene derivatives
inferred← citeshttps://doi.org/10.1039/d3ob00828bopenalex-snapshot
Ru( ii ) catalyzed chelation assisted C(sp 2 )–H bond functionalization along with concomitant (4 + 2) annulation
inferred← citeshttps://doi.org/10.1039/d4md00721bopenalex-snapshot
Design and synthesis of coumarin-based amphoteric antimicrobials with biofilm interference and immunoregulation effects
inferred← citeshttps://doi.org/10.1055/s-0037-1609909openalex-snapshot
Triethylamine — A Versatile Organocatalyst in Organic Transformations: A Decade Update
inferred← citeshttps://doi.org/10.1055/s-0043-1775454openalex-snapshot
Coumarin-Fused Nitrogenous Heterocycles: An Exploration of Annulation Strategies
inferred← citeshttps://doi.org/10.1080/00397911.2017.1336557openalex-snapshot
Green approach for the synthesis of 4-coumarin-4H-pyrans from 4-formylcoumarins and their antibacterial study
inferred← citeshttps://doi.org/10.1080/00397911.2020.1846058openalex-snapshot
Acetic acid promoted an efficient and eco-friendly one-pot synthesis of functionalized novel isoxazolyl amino chromenopyrrole derivatives in aqueous medium
inferred← citeshttps://doi.org/10.1080/00397911.2020.1846748openalex-snapshot
Efficient synthesis and characterization of novel bis(chromenes) and bis(benzo[f]chromenes) linked to thiazole units
inferred← citeshttps://doi.org/10.1080/00397911.2026.2659734openalex-snapshot
Synthesis and biological evaluation of coumarin-integrated heterocycles as potent antitumor agents
inferred← citeshttps://doi.org/10.1080/07328303.2014.941995openalex-snapshot
FeCl3·6H2O/C: An Efficient and Recyclable Catalyst for the Synthesis of 2,3-UnsaturatedO-andS-Glycosides
inferred← citeshttps://doi.org/10.1080/07328303.2020.1788575openalex-snapshot
FeCl3/C as an efficient catalyst for Ferrier rearrangement of 3,4,6-tri-O-Benzyl-D-glucal
inferred← citeshttps://doi.org/10.1080/10406638.2019.1576748openalex-snapshot
Poly(4-Vinylpyridine) (P4VPy): A Basic Catalyst for Facile Synthesis of Biscoumarin and Dihydropyrano[3,2-c]Chromene Derivatives in Aqueous Media
inferred← citeshttps://doi.org/10.1080/10406638.2021.2019801openalex-snapshot
Silica Chemisorbed Bis(Hydrogensulphato)Benzene (SiO 2 -BHSB) as a New, Environmentally Benign and Recyclable Catalyst for an Efficient Synthesis of Biscoumarin Scaffolds in Water Based Solvent
inferred← citeshttps://doi.org/10.1080/10426507.2010.520284openalex-snapshot
Development of New Sulfur-Containing Conjugated Compounds as Anti-HCV Agents
inferred← citeshttps://doi.org/10.1080/10426507.2014.952000openalex-snapshot
A Novel and Facile Methodology for Synthesis of Coumarin Coupled Benzimidazole-2-Thione Compounds
inferred← citeshttps://doi.org/10.1080/10426507.2021.1986503openalex-snapshot
Silica chemisorbed bis(hydrogensulphato)benzene (SiO 2 -BHSB) as a new, efficient, and recyclable catalyst for the synthesis of 5-oxopyrono[3,2- c ]chromene scaffolds in water-based solvent
inferred← citeshttps://doi.org/10.1080/14786419.2018.1519825openalex-snapshot
Evaluating the inhibitory effect of eight compounds from Daphne papyracea against the NS3/4A protease of hepatitis C virus
inferred← citeshttps://doi.org/10.1080/15376516.2021.1902030openalex-snapshot
A novel anticancer chromeno-pyrimidine analogue inhibits epithelial-mesenchymal transition in lung adenocarcinoma cells
inferred← citeshttps://doi.org/10.1080/15421406.2015.1011453openalex-snapshot
Synthesis, Characterization, and Antibacterial Activity of 7-Fluoro-2-oxo-2H-chromene-3-carboxylic Acid Ethyl Ester
inferred← citeshttps://doi.org/10.1080/15421406.2015.1038032openalex-snapshot
Synthesis, characterization, and antibacterial activity of 6-Chloro-8-methyl-2-oxo-2H-chromene-3-carboxylic acid ethyl ester
inferred← citeshttps://doi.org/10.1080/17518253.2018.1556743openalex-snapshot
Synthesis and cytotoxic activity of some novel benzocoumarin derivatives under solvent free conditions
inferred← citeshttps://doi.org/10.1107/s1600536810042005openalex-snapshot
4-Bromomethyl-6-methoxy-2H-chromen-2-one
inferred← citeshttps://doi.org/10.1107/s2056989016017217openalex-snapshot
Crystal structure of 7-hydroxy-8-[(4-methylpiperazin-1-yl)methyl]-2H-chromen-2-one
inferred← citeshttps://doi.org/10.1111/j.1747-0285.2012.01344.xopenalex-snapshot
Synthesis and Preliminary Biologic Evaluation of 5‐Substituted‐2‐(4‐substituted phenyl)‐1,3‐Benzoxazoles as A Novel Class of Influenza Virus A Inhibitors
inferred← citeshttps://doi.org/10.1111/j.2042-7158.2012.01571.xopenalex-snapshot
Targeting adenosine receptors with coumarins: synthesis and binding activities of amide and carbamate derivatives
inferred← citeshttps://doi.org/10.1111/jphp.12135openalex-snapshot
Synthesis and adenosine receptors binding affinities of a series of 3-arylcoumarins
inferred← citeshttps://doi.org/10.1111/jphp.13331openalex-snapshot
Benzothiazoles as potential antiviral agents
inferred← citeshttps://doi.org/10.1134/s1070428022060021openalex-snapshot
Allylation of Ketones with Methyl 3-(Bromomethyl)but-3-enoate. Synthesis of Bioactive Unsaturated Lactones Based on Benzo[f]coumarin and Its Derivatives
inferred← citeshttps://doi.org/10.1134/s1070428024060034openalex-snapshot
Synthesis of New Indole-Containing Benzo[f]coumarin Derivatives and Their Effect on the Proliferation and Redox State of Rat C6 Glioma Cells
inferred← citeshttps://doi.org/10.1155/2019/8693614openalex-snapshot
Development of New Multicomponent Reactions in Eco-Friendly Media-Greener Reaction and Expeditious Synthesis of Novel Bioactive Benzylpyranocoumarins
inferred← citeshttps://doi.org/10.1155/2021/6492346openalex-snapshot
Natural Coumarins: Exploring the Pharmacological Complexity and Underlying Molecular Mechanisms
inferred← citeshttps://doi.org/10.11606/d.17.2012.tde-16052012-203921openalex-snapshot
Estudo da atividade antioxidante de derivados 3-fenilcumarínicos no metabolismo oxidativo de neutrófilos humanos estimulados por complexos imunes
inferred← citeshttps://doi.org/10.1248/cpb.c12-00531openalex-snapshot
Design, Synthesis and Biological Evaluation of Novel 7-Mercaptocoumarin Derivatives as α1-Adrenoceptor Antagonists
inferred← citeshttps://doi.org/10.14233/ajchem.2020.22849openalex-snapshot
Zirconium(IV) Oxychloride: A Simple and Efficient Catalyst for the Synthesis of Chromen-2-one Derivatives
inferred← citeshttps://doi.org/10.1515/gps-2013-0114openalex-snapshot
A solvent free approach for Knoevenagel condensation: facile synthesis of 3-cyano and 3-carbethoxycoumarins
inferred← citeshttps://doi.org/10.1515/zkri-2016-2015openalex-snapshot
Syntheses of benzo[c]coumarin carboxylic acids and fluorescence properties in the solid state
inferred← citeshttps://doi.org/10.17660/actahortic.2016.1125.1openalex-snapshot
Metabolomic profiling of antiviralScaevola spinescensextracts by high resolution tandem mass spectrometry
inferred← citeshttps://doi.org/10.18520/cs/v118/i6/931-945openalex-snapshot
Averrhoa bilimbi in Organic Transformation:A Highly Efficient and Green Biosurfactant for the Synthesis of Multi-Functional Chromenes and Xanthenes
inferred← citeshttps://doi.org/10.2174/1381612811319210013openalex-snapshot
Current Developments of Coumarin Compounds in Medicinal Chemistry
inferred← citeshttps://doi.org/10.2174/1389557521666210927124511openalex-snapshot
A Review on Coumarin Derivatives as Potent Anti-tuberculosis Agents
inferred← citeshttps://doi.org/10.2174/156802612805220002openalex-snapshot
Focusing on New Monoamine Oxidase Inhibitors: Differently Substituted Coumarins As An Interesting Scaffold
inferred← citeshttps://doi.org/10.2174/1570178618666210202152452openalex-snapshot
Synthesis and Biological Properties of Coumarin Analogue: A Brief Review
inferred← citeshttps://doi.org/10.24272/j.issn.2095-8137.2020.037openalex-snapshot
Hydroxycoumarin efficiently inhibits spring viraemia of carp virus infection in vitro and in vivo
inferred← citeshttps://doi.org/10.3109/14756366.2014.979346openalex-snapshot
Design, synthesis and bioevaluation of novel umbelliferone analogues as potential mushroom tyrosinase inhibitors
inferred← citeshttps://doi.org/10.33224/rrch.2020.65.5.07openalex-snapshot
Efficient synthesis of bis-(4-hydroxycoumarin) using sulfanilic acid as recyclable catalyst in water
inferred← citeshttps://doi.org/10.3390/ecsoc-16-01041openalex-snapshot
Multi-target Design, Synthesis and Study of a Selected Series of Carbamates and Esters with Coumarin Scaffold
inferred← citeshttps://doi.org/10.3390/ecsoc-18-b023openalex-snapshot
Structural Modifications on Natural-based Products: Synthetic Strategies and Biological Applications
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