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Tyrosinase Inhibitory Activity of the Olive Oil Flavor Compounds

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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/jsfa.2740250306openalex-snapshot
Inhibition by carboxylic acids of an o‐diphenol oxidase from Prunus avium fruits
inferredcites →https://doi.org/10.1007/bf01948015openalex-snapshot
Potentiation of antifungal activity of sesquiterpene dialdehydes againstCandida albicans and two other fungi
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The Hydrophobic Effect: Formation of Micelles and Biological Membranes
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Naturally occurring carbonyl compounds are mutagens Salmonella tester strain TA104
inferredcites →https://doi.org/10.1016/0167-4838(94)00204-topenalex-snapshot
Tyrosinase: a comprehensive review of its mechanism
inferredcites →https://doi.org/10.1016/0968-0896(95)00081-qopenalex-snapshot
Structural functions of antimicrobial long-chain alcohols and phenols
inferredcites →https://doi.org/10.1021/bi00185a010openalex-snapshot
Inhibitor Binding to the Binuclear Active Site of Tyrosinase: Temperature, pH, and Solvent Deuterium Isotope Effects
inferredcites →https://doi.org/10.1021/bk-1997-0658openalex-snapshot
Phytochemicals for Pest Control
inferredcites →https://doi.org/10.1021/ja00299a043openalex-snapshot
Substrate analog binding to the coupled binuclear copper active site in tyrosinase
inferredcites →https://doi.org/10.1021/jf00043a033openalex-snapshot
Structure-Antifungal Activity Relationships among Volatile C6 and C9 Aliphatic Aldehydes, Ketones, and Alcohols
inferredcites →https://doi.org/10.1021/jf60190a030openalex-snapshot
Aroma components of olive oil
inferredcites →https://doi.org/10.1021/jf60190a031openalex-snapshot
Thin-layer chromatographic investigation of color developer involved in pinking of white onion purees
inferredcites →https://doi.org/10.1055/s-1999-13955openalex-snapshot
2-Hydroxy-4-methoxybenzaldehyde: A Potent Tyrosinase Inhibitor from African Medicinal Plants
inferredcites →https://doi.org/10.1055/s-2008-1074986openalex-snapshot
Inhibitory Effect of Chinese Crude Drugs on Tyrosinase
inferredcites →https://doi.org/10.1111/j.1365-2133.1981.tb00752.xopenalex-snapshot
Molecular basis of substrate and inhibitory specificity of tyrosinase: phenolic compounds
inferredcites →https://doi.org/10.4269/ajtmh.1983.32.6.tm0320061468aopenalex-snapshot
Update: Dermatology in General Medicine
inferredcites →https://doi.org/10.5860/choice.33-5091openalex-snapshot
Food enzymes: structure and mechanism

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.4760920openalex-extracted
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inferred← citeshttps://doi.org/10.1002/aoc.7510openalex-snapshot
High anticancer activity in short response time exhibited by a new azobenzene derivative and its copper complex
inferred← citeshttps://doi.org/10.1002/cbdv.201300066openalex-snapshot
Chemical Composition and Antimicrobial Activity of the Essential Oil from the Edible Aromatic Plant Aristolochia delavayi
inferred← citeshttps://doi.org/10.1002/cbdv.201900167openalex-snapshot
Phosphonic and Phosphinic Acid Derivatives as Novel Tyrosinase Inhibitors: Kinetic Studies and Molecular Docking
inferred← citeshttps://doi.org/10.1002/jsfa.5605openalex-snapshot
Effect of cinnamaldehyde on melanosis and spoilage of Pacific white shrimp (Litopenaeus vannamei) during storage
inferred← citeshttps://doi.org/10.1002/ptr.1428openalex-snapshot
In vitro anti‐tyrosinase activity of 5‐(hydroxymethyl)‐2‐furfural isolated from Dictyophora indusiata
inferred← citeshttps://doi.org/10.1002/qua.22968openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/vjch.70152openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-1-4020-5670-3_24openalex-snapshot
Antimicrobial browning-inhibitory effect of flavor compounds in seaweeds
inferred← citeshttps://doi.org/10.1007/s00018-005-5054-yopenalex-snapshot
Tyrosinase inhibitors from natural and synthetic sources: structure, inhibition mechanism and perspective for the future
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inferred← citeshttps://doi.org/10.1007/s10811-006-9046-6openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s11426-025-2692-xopenalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s11483-025-10004-9openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s12010-007-8007-0openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s12562-019-01376-2openalex-snapshot
Selenoneine suppresses melanin synthesis by inhibiting tyrosinase in murine B16 melanoma cells and 3D-cultured human melanocytes
inferred← citeshttps://doi.org/10.1016/j.bbapap.2011.12.012openalex-snapshot
Extracellular tyrosinase from the fungus Trichoderma reesei shows product inhibition and different inhibition mechanism from the intracellular tyrosinase from Agaricus bisporus
inferred← citeshttps://doi.org/10.1016/j.bcab.2020.101819openalex-snapshot
Phenolic contents and in vitro investigation of the antioxidant, enzyme inhibitory, photoprotective, and antimicrobial effects of the organic extracts of Pelargonium graveolens growing in Morocco
inferred← citeshttps://doi.org/10.1016/j.bioorg.2024.107722openalex-snapshot
Kinetic studies, molecular docking, and antioxidant activity of novel 1,3-diphenyl pyrazole-thiosemicarbazone with anti-tyrosinase and anti-melanogenesis properties
inferred← citeshttps://doi.org/10.1016/j.bmc.2003.11.014openalex-snapshot
QSAR and kinetics of the inhibition of benzaldehyde derivatives against Sacrophaga neobelliaria phenoloxidase
inferred← citeshttps://doi.org/10.1016/j.bmc.2007.01.035openalex-snapshot
Identification of tyrosinase inhibitors from Marrubium velutinum and Marrubium cylleneum
inferred← citeshttps://doi.org/10.1016/j.bmc.2012.12.053openalex-snapshot
Synthesis of new heterocyclic hybrids based on pyrazole and thiazolidinone scaffolds as potent inhibitors of tyrosinase
inferred← citeshttps://doi.org/10.1016/j.bmc.2014.04.060openalex-snapshot
Design, synthesis and biological evaluation of hydroxy- or methoxy-substituted 5-benzylidene(thio) barbiturates as novel tyrosinase inhibitors
inferred← citeshttps://doi.org/10.1016/j.bmc.2015.01.024openalex-snapshot
Rational design, synthesis and structure–activity relationships of 4-alkoxy- and 4-acyloxy-phenylethylenethiosemicarbazone analogues as novel tyrosinase inhibitors
inferred← citeshttps://doi.org/10.1016/j.bmc.2015.06.068openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.bmc.2018.07.014openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.bmcl.2003.11.033openalex-snapshot
2-Hydroxy-4-isopropylbenzaldehyde, a potent partial tyrosinase inhibitor
inferred← citeshttps://doi.org/10.1016/j.bmcl.2010.08.018openalex-snapshot
Synthesis and biological evaluation of a novel series of bis-salicylaldehydes as mushroom tyrosinase inhibitors
inferred← citeshttps://doi.org/10.1016/j.bmcl.2012.10.107openalex-snapshot
Synthesis and dual biological effects of hydroxycinnamoyl phenylalanyl/prolyl hydroxamic acid derivatives as tyrosinase inhibitor and antioxidant
inferred← citeshttps://doi.org/10.1016/j.cbi.2025.111888openalex-snapshot
Structural diversity of aldehydes determines covalent versus non-covalent inhibition mechanisms against steroid 5α-reductase type 1: Species-specific differences and preliminary structure-activity relationships
inferred← citeshttps://doi.org/10.1016/j.ejmech.2009.11.007openalex-snapshot
Synthesis and biological evaluation of novel 4-hydroxybenzaldehyde derivatives as tyrosinase inhibitors
inferred← citeshttps://doi.org/10.1016/j.ejmech.2013.05.040openalex-snapshot
A novel one-pot synthesis and preliminary biological activity evaluation of cis-restricted polyhydroxy stilbenes incorporating protocatechuic acid and cinnamic acid fragments
inferred← citeshttps://doi.org/10.1016/j.ejmech.2015.02.013openalex-snapshot
Structure-based modification of 3-/4-aminoacetophenones giving a profound change of activity on tyrosinase: From potent activators to highly efficient inhibitors
inferred← citeshttps://doi.org/10.1016/j.ejmech.2017.08.033openalex-snapshot
Study on the design, synthesis and structure-activity relationships of new thiosemicarbazone compounds as tyrosinase inhibitors
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.ica.2018.03.032openalex-snapshot
Coordination susceptibilities of cinnamaldehyde and cuminaldehyde derived Schiff bases towards the fac-[Re(CO)3]+ core: Formation, computational and DNA interaction studies
inferred← citeshttps://doi.org/10.1016/j.ica.2018.12.031openalex-snapshot
DNA interaction and anticancer evaluation of new zinc(II), ruthenium(II), rhodium(III), palladium(II), silver(I) and platinum(II) complexes based on kojic acid; X-ray crystal structure of [Ag(ka)(PPh3)]·H2O
inferred← citeshttps://doi.org/10.1016/j.ifset.2014.11.001openalex-snapshot
Citrus hydrosols as useful by-products for tyrosinase inhibition
inferred← citeshttps://doi.org/10.1016/j.indcrop.2013.10.053openalex-snapshot
Evaluating tyrosinase (monophenolase) inhibitory activity from fragrant roots of Hemidesmus indicus for potent use in herbal products
inferred← citeshttps://doi.org/10.1016/j.indcrop.2020.112654openalex-snapshot
Evaluation of the incorporation of essential oils in microemulsions as a promising formulation in the inhibition of tyrosinase
inferred← citeshttps://doi.org/10.1016/j.jchromb.2006.08.046openalex-snapshot
Gel electrophoresis of polyphenol oxidase with instant identification by in situ blotting
inferred← citeshttps://doi.org/10.1016/j.molstruc.2021.131933openalex-snapshot
Flavone-based hydrazones as new tyrosinase inhibitors: Synthetic imines with emerging biological potential, SAR, molecular docking and drug-likeness studies
inferred← citeshttps://doi.org/10.1016/j.poly.2017.12.013openalex-snapshot
A gap is filled: First structures of enantiopure iron(III) complexes with Schiff base ligands derived from ortho-vanillin and -glutamine or l-glutamic acid
inferred← citeshttps://doi.org/10.1016/j.procbio.2011.06.005openalex-snapshot
Physiological properties of tuna cooking drip hydrolysate prepared with gamma irradiation
inferred← citeshttps://doi.org/10.1016/j.procbio.2016.09.019openalex-snapshot
Inhibitory mechanism of cardanols on tyrosinase
inferred← citeshttps://doi.org/10.1016/s0378-1097(01)00089-1openalex-snapshot
In vitro antibacterial activity of some aliphatic aldehydes from Olea europaea L.
inferred← citeshttps://doi.org/10.1016/s0968-0896(01)00084-0openalex-snapshot
Hydroxy- or Methoxy-Substituted Benzaldoximes and Benzaldehyde-O-alkyloximes as Tyrosinase Inhibitors
inferred← citeshttps://doi.org/10.1016/s1357-2725(03)00006-2openalex-snapshot
Inhibitory effects of cupferron on the monophenolase and diphenolase activity of mushroom tyrosinase
inferred← citeshttps://doi.org/10.1021/jf072893lopenalex-snapshot
Identification of Geranic Acid, a Tyrosinase Inhibitor in Lemongrass (Cymbopogon citratus)
inferred← citeshttps://doi.org/10.1021/jf1033625openalex-snapshot
Inhibition Kinetics of Chlorobenzaldehyde Thiosemicarbazones on Mushroom Tyrosinase
inferred← citeshttps://doi.org/10.1021/jf505469kopenalex-snapshot
Alpha-Substituted Derivatives of Cinnamaldehyde as Tyrosinase Inhibitors: Inhibitory Mechanism and Molecular Analysis
inferred← citeshttps://doi.org/10.1039/c9md00005dopenalex-snapshot
Thiosemicarbazones with tyrosinase inhibitory activity
inferred← citeshttps://doi.org/10.1080/00268976.2017.1335896openalex-snapshot
Electronic structure and acid–base properties of Kojic acid and its dimers. A DFT and quantum topology study
inferred← citeshttps://doi.org/10.1080/01496395.2018.1444052openalex-snapshot
Simultaneous recovery of glycyrrhizic acid and liquiritin from Chinese licorice root ( Glycyrrhiza uralensis Fisch) by aqueous two-phase system and evaluation biological activities of extracts
inferred← citeshttps://doi.org/10.1080/10408398.2021.1871724openalex-snapshot
A systematic review of synthetic tyrosinase inhibitors and their structure-activity relationship
inferred← citeshttps://doi.org/10.1080/10937400600882871openalex-snapshot
Inhibitory Effects of Plant Extracts on Tyrosinase, l -DOPA Oxidation, and Melanin Synthesis
inferred← citeshttps://doi.org/10.1080/14756360409162449openalex-snapshot
Mushroom Tyrosinase Inhibition by Two Potent Uncompetitive Inhibitors
inferred← citeshttps://doi.org/10.1080/14756360903179351openalex-snapshot
Potent inhibitory effects of benzyl andp-xylidine-bis dithiocarbamate sodium salts on activities of mushroom tyrosinase
inferred← citeshttps://doi.org/10.1080/14756366.2016.1256882openalex-snapshot
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inferred← citeshttps://doi.org/10.1080/14756366.2022.2061966openalex-snapshot
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inferred← citeshttps://doi.org/10.1080/14786419.2016.1253076openalex-snapshot
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inferred← citeshttps://doi.org/10.1093/jn/133.8.2532openalex-snapshot
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inferred← citeshttps://doi.org/10.1111/cbdd.13352openalex-snapshot
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inferred← citeshttps://doi.org/10.1111/j.1745-4514.2010.00434.xopenalex-snapshot
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inferred← citeshttps://doi.org/10.1111/jfpp.17058openalex-snapshot
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inferred← citeshttps://doi.org/10.11301/jsfe.10.149openalex-snapshot
Inhibitory Effects of Sechium edule Extract on Melannin Synthesis in a Human Skin Model
inferred← citeshttps://doi.org/10.1155/2015/541591openalex-snapshot
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inferred← citeshttps://doi.org/10.1155/2022/4806889openalex-snapshot
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inferred← citeshttps://doi.org/10.1186/1999-3110-54-10openalex-snapshot
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inferred← citeshttps://doi.org/10.1201/9781420059946.ch9openalex-snapshot
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inferred← citeshttps://doi.org/10.1248/cpb.c19-00949openalex-snapshot
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inferred← citeshttps://doi.org/10.13005/bpj/2229openalex-snapshot
Microbial Tyrosinase: Biochemical, Molecular Properties and Pharmaceutical Applications
inferred← citeshttps://doi.org/10.1351/pac200779122277openalex-snapshot
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inferred← citeshttps://doi.org/10.18174/38558openalex-snapshot
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inferred← citeshttps://doi.org/10.21608/jpp.2014.53642openalex-snapshot
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inferred← citeshttps://doi.org/10.3109/14756360903179351openalex-snapshot
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inferred← citeshttps://doi.org/10.3109/14756360903476398openalex-snapshot
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inferred← citeshttps://doi.org/10.3184/146867813x13590434110159openalex-snapshot
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inferred← citeshttps://doi.org/10.32439/ps.v5i2.36-44openalex-snapshot
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inferred← citeshttps://doi.org/10.3389/fpls.2023.1284931openalex-snapshot
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inferred← citeshttps://doi.org/10.3389/fsufs.2022.1001362openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/ijms10062440openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/ijms12010506openalex-snapshot
The Biochemical and Cellular Basis for Nutraceutical Strategies to Attenuate Neurodegeneration in Parkinson’s Disease
inferred← citeshttps://doi.org/10.3390/plants10050969openalex-snapshot
Citral-Containing Essential Oils as Potential Tyrosinase Inhibitors: A Bio-Guided Fractionation Approach
inferred← citeshttps://doi.org/10.3839/jabc.2015.047openalex-snapshot
Tyrosinase Inhibitory Activities of Safrole fromMyristica fragransHoutt.
inferred← citeshttps://doi.org/10.3906/kim-2005-51openalex-snapshot
Chemical composition, antimicrobial, and lipase enzyme activity of essential oil and solvent extracts from Serapiasorientalis subsp. orientalis
inferred← citeshttps://doi.org/10.4236/ijoc.2012.24054openalex-snapshot
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inferred← citeshttps://doi.org/10.4315/0362-028x.jfp-13-323openalex-snapshot
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inferred← citeshttps://doi.org/10.5021/ad.2016.28.5.555openalex-snapshot
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inferred← citeshttps://doi.org/10.7841/ksbbj.2012.27.3.195openalex-snapshot
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