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Oxazolones: New tyrosinase inhibitors; synthesis and their structure–activity relationships

https://doi.org/10.1016/j.bmc.2006.05.014
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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/cbdv.200590027openalex-snapshot
Synthesis of Methyl Ether Analogues of Sildenafil (Viagra®) Possessing Tyrosinase Inhibitory Potential
inferredcites →https://doi.org/10.1002/jhet.5570200320openalex-snapshot
Reaction of 4‐methylene‐5(4H)‐oxazolones with diazomethane
inferredcites →https://doi.org/10.1002/jhet.5570310406openalex-snapshot
Studies on isocyanides and related compounds. An unusual synthesis of imidazolyloxazolones
inferredcites →https://doi.org/10.1007/bf02979054openalex-snapshot
Relationship between tyrosinase inhibitory action and oxidation-reduction potential of cosmetic whitening ingredients and phenol derivatives
inferredcites →https://doi.org/10.1007/s11030-005-1299-5openalex-snapshot
A facile and improved synthesis of sildenafil (Viagra�) analogs through solid support microwave irradiation possessing tyrosinase inhibitory potential, their conformational analysis and molecular dynamics simulation studies
inferredcites →https://doi.org/10.1016/0040-4020(66)80098-4openalex-snapshot
Syntheses from pyridine aldehydes—I
inferredcites →https://doi.org/10.1016/0040-4020(95)00501-xopenalex-snapshot
Z -2-Phenyl-4-[(S)- 2,2-dimethyl-1,3-dioxolan-4-ylmethylen]-5(4H)-oxazolone as the Dienophile in Asymmetric Diels-Alder Reactions
inferredcites →https://doi.org/10.1016/0040-4020(96)00522-4openalex-snapshot
Conformationally constrained tryptophan analogs. Synthesis of (±)-(Z)- and (±)-(E)-2-amino-2,3-methano-3-(indol-3-yl)-propanoic acids
inferredcites →https://doi.org/10.1016/0957-4166(96)00295-9openalex-snapshot
Diels-Alder reactions of (E)-2-phenyl-4-[(S)-2,2-dimethyl-1,3-dioxolan-4-ylmethylen]-5(4H)-oxazolone with heterogeneous catalysts
inferredcites →https://doi.org/10.1016/j.bmc.2004.02.034openalex-snapshot
Synthesis and immunomodulatory properties of selected oxazolone derivatives
inferredcites →https://doi.org/10.1016/j.bmc.2005.03.012openalex-snapshot
Structure–activity relationships of tyrosinase inhibitory combinatorial library of 2,5-disubstituted-1,3,4-oxadiazole analogues
inferredcites →https://doi.org/10.1016/j.bmc.2005.08.029openalex-snapshot
Tetraketones: A new class of tyrosinase inhibitors
inferredcites →https://doi.org/10.1016/s0040-4020(01)92303-8openalex-snapshot
A novel preparation of pseudoxazolones
inferredcites →https://doi.org/10.1016/s0040-4020(01)98494-7openalex-snapshot
Some 2-fluoroethylamines derived from hydrocinnamic acid, phenylpyruvic acid and DL-phenylalanine
inferredcites →https://doi.org/10.1016/s0040-4020(96)01101-5openalex-snapshot
5(4H)-Oxazolones. Part X. Acid and base effects on the translactonization reaction of 4-(2-Oxa-alkylidene)-5(4H)-oxazolones: New synthesis of 5-alkylidene-3-benzoylamino-2(5H)-furanones
inferredcites →https://doi.org/10.1016/s0040-4020(97)00120-8openalex-snapshot
1,3-Dipolar cycloaddition of diazomethane to chiral azlactones. Experimental and theoretical studies
inferredcites →https://doi.org/10.1016/s0040-4020(97)00456-0openalex-snapshot
Resolution of racemic carboxylic acid derivatives by Ti-TADDOLate mediated esterification reactions—A general method for the preparation of enantiopure compounds
inferredcites →https://doi.org/10.1016/s0040-4020(98)01064-3openalex-snapshot
Ring opening with kinetic resolution of azlactones by Ti-TADDOLates
inferredcites →https://doi.org/10.1016/s0040-4039(98)01031-4openalex-snapshot
Fluorescent properties of model chromophores of tyrosine-66 substituted mutants of Aequorea green fluorescent protein (GEP)
inferredcites →https://doi.org/10.1016/s0957-4166(97)00016-5openalex-snapshot
Asymmetric synthesis of l-thienylalanines
inferredcites →https://doi.org/10.1021/ja01611a042openalex-snapshot
Synthesis of 2,2'-Bis-[5(4H)-oxazolones]
inferredcites →https://doi.org/10.1021/jf011230fopenalex-snapshot
Tyrosinase Inhibitors of Pulsatilla cernua Root-Derived Materials
inferredcites →https://doi.org/10.1021/jo00866a037openalex-snapshot
Reactions in polyphosphoric acid. I. New stereospecific synthesis of the E isomers of 2-phenyl-4-arylmethylene-2-oxazolin-5-ones
inferredcites →https://doi.org/10.1021/jo951213nopenalex-snapshot
A New Synthesis of Functionalized 2-Alkylidenetetrahydro-5-furanones by Tandem Alkylation and Translactonization Reactions of 5(4H)-Oxazolones
inferredcites →https://doi.org/10.1021/np50106a021openalex-snapshot
Tyrosinase Inhibitors from Anacardium occidentale Fruits
inferredcites →https://doi.org/10.1039/c39880000790openalex-snapshot
The fluorescence of the chromophore of the green fluorescent protein of Aequorea and Renilla
inferredcites →https://doi.org/10.1039/p19940002499openalex-snapshot
Reaction of 2, 4- diphenyl-4, 5-dihydro-1, 3-oxazol-5-one with 4-phenyl-N-tosyl-1azabuta-1, 3-diene; CC versus CN double bond addition
inferredcites →https://doi.org/10.1080/14756360500179333openalex-snapshot
Tyrosinase inhibition: Conformational analysis based studies on molecular dynamics calculations of bipiperidine based inhibitors
inferredcites →https://doi.org/10.1111/j.1600-0749.1999.tb00756.xopenalex-snapshot
Effects of 4‐Tertiary Butylphenol on the Tyrosinase Activity in Human Melanocytes
inferredcites →https://doi.org/10.1271/bbb.67.631openalex-snapshot
Mushroom Tyrosinase Inhibitory Activity of Esculetin Isolated from Seeds of Euphorbia lathyris L.
inferredcites →https://doi.org/10.2174/1570180054771554openalex-snapshot
Immunomodulatory Properties of Synthetic Imidazolone Derivatives

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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5(4H)‐Oxazolones as Novel Antitubercular Agents: Synthesis, Characterisation and Structure Activity Study
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Synthesis of Novel Heterocycles Derived from 4‐Arylmethylene‐2‐phenyl‐1,3‐oxazole‐5(4H)‐ones
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Action of Some Nitrogen and Carbon Nucleophils on 4‐Arylidene‐1,3‐oxazolones
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Dependence of the anticancer activity of 1,3‐oxazole derivatives on the donor/acceptor nature of his substitues
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Efficient synthesis and characterization of novel bis‐heterocyclic derivatives and benzo‐fused macrocycles containing oxazolone or imidazolone subunits
inferred← citeshttps://doi.org/10.1002/jhet.499openalex-snapshot
Synthesis of novel carbazolyl‐oxazolone derivatives and their spectroscopic properties
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A facile synthesis of 2‐alkyl‐3‐α‐carboxy‐α‐styryl/heterylvinyl quinazolin‐4(3H)‐ones and 3‐arylidene/heterylmethylidene‐4‐aroyl‐1H‐[1,4]benzodiazepine‐2,5(3H,4H)‐diones and their transformation into novel heterocyclyl and heterocyclo analogues
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Design and Synthesis of New Quinoxaline‐Oxazole‐Morpholino Conjugates; Evaluation of Anticancer Activity and In Silico Molecular Docking and ADMET Studies
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Method validation of 15 phytochemicals in Hypericum lysimachioides var. spathulatum by LC–MS/MS, and fatty acid, essential oil, and aroma profiles with biological activities
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Synthesis of 6-deoxymollugins and their inhibitory activities on tyrosinase
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An efficient synthesis of some novel oxazolone derivatives showing cytotoxic activity
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Oxazolone
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Organic–inorganic hybrid polyoxometalates: Efficient, heterogeneous and reusable catalysts for solvent-free synthesis of azlactones
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Synthesis, characterization, antioxidant power and acute toxicity of some new azo-benzamide and azo-imidazolone derivatives with in vivo and in vitro antimicrobial evaluation
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Highly potent anti-melanogenic effect of 2-thiobenzothiazole derivatives through nanomolar tyrosinase activity inhibition
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Kinetic studies, molecular docking, and antioxidant activity of novel 1,3-diphenyl pyrazole-thiosemicarbazone with anti-tyrosinase and anti-melanogenesis properties
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Effects of Acmella oleracea methanolic extract and fractions on the tyrosinase enzyme
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Identification of tyrosinase inhibitors from Marrubium velutinum and Marrubium cylleneum
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Design and synthesis of biphenyl derivatives as mushroom tyrosinase inhibitors
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Design and synthesis of 3,5-diaryl-4,5-dihydro-1H-pyrazoles as new tyrosinase inhibitors
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Synthesis of novel azo compounds containing 5(4H)-oxazolone ring as potent tyrosinase inhibitors
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Design and synthesis of thiourea derivatives with sulfur-containing heterocyclic scaffolds as potential tyrosinase inhibitors
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Ketonethiosemicarbazones: Structure–activity relationships for their melanogenesis inhibition
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Structure–activity relationship of naphthaldehydethiosemicarbazones in melanogenesis inhibition
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Design, synthesis and molecular simulation studies of dihydrostilbene derivatives as potent tyrosinase inhibitors
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Microwave-assisted efficient synthesis of azlactone derivatives using 2-aminopyridine-functionalized sphere SiO2 nanoparticles as a reusable heterogeneous catalyst
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One-pot Vilsmeier reagent-mediated multicomponent reaction: A direct synthesis of oxazolones and Erlenmeyer azlactones from carboxylic acids
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The synthesis, structure and spectroscopic properties of novel oxazolone-, pyrazolone- and pyrazoline-containing heterocycle chromophores
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Synthesis, characterization and evaluation of the photophysical and nonlinear optical behaviour of novel 4-substituted arylidene-2-[5-(2,6-dichlorophenyl)-3-methyl-1,2-oxazol-4-yl]-1,3-oxazol-5-ones
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Green fluorescent protein chromophore derivatives as a new class of aldose reductase inhibitors
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Design, synthesis, kinetic mechanism and molecular docking studies of novel 1-pentanoyl-3-arylthioureas as inhibitors of mushroom tyrosinase and free radical scavengers
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Selective in vitro and in silico enzymes inhibitory activities of phenolic acids and flavonoids of food plants: Relations with oxidative stress
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A detailed study on chemical and biological profile of nine Euphorbia species from Turkey with chemometric approach: Remarkable cytotoxicity of E. fistulasa and promising tannic acid content of E. eriophora
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Determination of antioxidant, cytotoxic, anticholinesterase, antiurease, antityrosinase, and antielastase activities and aroma, essential oil, fatty acid, phenolic, and terpenoid-phytosterol contents of Salvia poculata
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5-Methoxy-2-mercaptobenzimidazole as an efficient inhibitor on tyrosinase: Inhibitory activity and mechanism
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Photophysical and optical properties of 4-(4'-(diphenylamino)benzylidene)-2-phenyloxazol-5(4H)-ones induced by the peripheral substituent
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A comprehensive LC–MS/MS method validation for the quantitative investigation of 37 fingerprint phytochemicals in Achillea species: A detailed examination of A. coarctata and A. monocephala
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Application of the pyrazolone derivatives as effective modulators in the opto-electronic networks
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New spiropyrrolothiazole derivatives bearing an oxazolone moiety as potential antidiabetic agent: Design, synthesis, crystal structure, Hirshfeld surface analysis, ADME and molecular docking studies
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Antimetastatic activity evaluation of diamides inspired by SRPK inhibitor N-[2-(piperidin-1-yl)-5-(trifluoromethyl) phenyl] isonicotinamide (SRPIN340)
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Experimental and theoretical studies of the influence of solvent polarity on the spectral properties of two push-pull oxazol-5-(4 H )-one compounds
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Synthesis of new steroidal derivatives by the reaction of steroid–amino acid conjugates with N,N′-dicyclohexyl-carbodiimide. Unusual formation of steroidal imide derivatives
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Synthesis of new 2-substituted pyrazolo[5,1- b ][1,3]oxazoles via Sonogashira coupling reactions in water
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Synthesis of multi-functionalized 1-azabicycles through MAOS acid catalyzed formal aza-[3+3] cycloaddition of heterocyclic enaminones with oxazolones
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Synthesis of Green Fluorescent Protein Chromophore Analogues for Interdisciplinary Learning for High School Students
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Multifunctional Oxazolone Derivative as an Optical Amplifier, Generator, and Modulator
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Synthesis of a Biologically Active Oxazol-5-(4H)-one via an Erlenmeyer–Plöchl Reaction
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4.2.3.7. Synthesis of a Biologically Active Oxazol-5(4H)-One via Erlenmeyer–Plöchl Reaction
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Alkynylation of heterocyclic compounds using hypervalent iodine reagent
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[Et 3 NH][HSO 4 ]-mediated functionalization of hippuric acid: an unprecedented approach to 4-arylidene-2-phenyl-5(4H)-oxazolones
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Synthesis, photophysical and biological properties of a new oxazolone fluorescent probe for bioimaging: an experimental and theoretical study
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An ionic liquid gel: a heterogeneous catalyst for Erlenmeyer–Plochl and Henry reactions
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Greener approach: Ionic liquid [Et3NH][HSO4]-catalyzed multicomponent synthesis of 4-arylidene-2-phenyl-5(4H)oxazolones under solvent-free condition
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SAR and QSAR research on tyrosinase inhibitors using machine learning methods
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Biological activity of the azlactone derivative EPA-35 against Trypanosoma cruzi
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2,6-Dimethoxy-4-(5-oxo-2-phenyl-4,5-dihydro-1,3-oxazol-4-ylidenemethyl)phenyl acetate
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2-Phenyl-4-(3,4,5-trimethoxybenzylidene)-1,3-oxazol-5(4H)-one
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1-(2-Hydroxy-2-phenylethyl)-3-(4-methoxyphenyl)urea
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(4Z)-4-Benzylidene-2-phenyl-1,3-oxazol-5(4H)-one
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Selective in-vitro Enzymes' Inhibitory Activities of Fingerprints Compounds of Salvia Species and Molecular Docking Simulations.
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An eco-compatible access to diversified bisoxazolone and bisimidazole derivatives
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Synthesis and leishmanicidal activity of 2,3,4-substituted-5-imidazolones
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Natural, semisynthetic and synthetic tyrosinase inhibitors
inferred← citeshttps://doi.org/10.33263/briac125.64606486openalex-snapshot
Synthetic Approaches and Biological Significance of Oxazolone Moieties: A Review
inferred← citeshttps://doi.org/10.3390/covid6060099openalex-snapshot
Synthesis and Structural Characterization of Substituted 4-Alkynyloxazolones: In Silico Insights on the Interaction with SARS-CoV-2 Spike Glycoprotein
inferred← citeshttps://doi.org/10.3390/ijms10062440openalex-snapshot
An Updated Review of Tyrosinase Inhibitors
inferred← citeshttps://doi.org/10.3390/molecules13123246openalex-snapshot
Dodecatungstophosphoric Acid (H3PW12O40), Samarium and Ruthenium (ІІІ) Chloride Catalyzed Synthesis of Unsaturated 2-Phenyl-5(4H)-oxazolone Derivatives under Solvent-free Conditions
inferred← citeshttps://doi.org/10.3390/molecules17056100openalex-snapshot
Synthesis and Evaluation of New β-Carboline-3-(4-benzylidene)-4H-oxazol-5-one Derivatives as Antitumor Agents
inferred← citeshttps://doi.org/10.3390/molecules23071545openalex-snapshot
Synthesis, Immunosuppressive Properties, and Mechanism of Action of a New Isoxazole Derivative
inferred← citeshttps://doi.org/10.3390/molecules25143173openalex-snapshot
5-(4H)-Oxazolones and Their Benzamides as Potential Bioactive Small Molecules
inferred← citeshttps://doi.org/10.3390/molecules27030671openalex-snapshot
Synthesis, Antimicrobial, Anti-Virulence and Anticancer Evaluation of New 5(4H)-Oxazolone-Based Sulfonamides
inferred← citeshttps://doi.org/10.3987/com-17-13711openalex-snapshot
Synthesis of Erlenmeyer-Plöchl Azlactones Promoted by 5-Sulfosalicylic Acid
inferred← citeshttps://doi.org/10.3987/com-17-13847openalex-snapshot
Sulfanilic Acid-Catalyzed Green Synthesis of 4-Arylidene-2-phenyl-5(4H)-oxazolones
inferred← citeshttps://doi.org/10.4314/bcse.v38i5.15openalex-snapshot
Design, synthesis and molecular docking study of novel bis-oxazolone derivatives as potent antioxidant and antibacterial agents
inferred← citeshttps://doi.org/10.4314/ijs.v20i1.1openalex-snapshot
Synthesis, antimicrobial activities and computational studies of some oxazolone derivatives
inferred← citeshttps://doi.org/10.47328/ufvbbt.2022.428openalex-snapshot
Efeito do inibidor de serine arginine protein kinases (SRPKS) SRPIN340 e derivados em células murinas de câncer de mama metastático
inferred← citeshttps://doi.org/10.51847/pjewevbopenalex-snapshot
10.51847/PjEwEvb
inferred← citeshttps://doi.org/10.52711/2231-5691.2023.00028openalex-snapshot
Design, Synthesis, Characterization and Non-steroidal Anti-Inflammatory Activity of Novel Oxazolone Derivatives
inferred← citeshttps://doi.org/10.55730/1300-008x.2723openalex-snapshot
Chemical fingerprints and bioactivities of 12 Anatolian Achillea species by LC-MS/MS with chemometric approach: Novel phytonutrients, natural food preservatives and chlorogenic acid sources
inferred← citeshttps://doi.org/10.5772/46230openalex-snapshot
Non-Traditional Pesticidally Active Compounds
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