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Design, synthesis and molecular simulation studies of dihydrostilbene derivatives as potent tyrosinase inhibitors
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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Naturally occurring tyrosinase inhibitors: mechanism and applications in skin health, cosmetics and agriculture industries
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Dopamine- or L-DOPA-induced neurotoxicity: The role of dopamine quinone formation and tyrosinase in a model of Parkinson’s disease
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Tyrosinase inhibitors from natural and synthetic sources: structure, inhibition mechanism and perspective for the future
inferredcites →https://doi.org/10.1016/j.bbapap.2008.07.002openalex-snapshot
Oxidative metabolism of dopamine: A colour reaction from human midbrain analysed by mass spectrometry
inferredcites →https://doi.org/10.1016/j.bmc.2005.09.010openalex-snapshot
Tyrosinase inhibitory cycloartane type triterpenoids from the methanol extract of the whole plant of Amberboa ramosa Jafri and their structure–activity relationship
inferredcites →https://doi.org/10.1016/j.bmc.2006.05.014openalex-snapshot
Oxazolones: New tyrosinase inhibitors; synthesis and their structure–activity relationships
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Identification of tyrosinase inhibitors from Marrubium velutinum and Marrubium cylleneum
inferredcites →https://doi.org/10.1016/j.bmcl.2006.01.022openalex-snapshot
Analogues of N-hydroxycinnamoylphenalkylamides as inhibitors of human melanocyte-tyrosinase
inferredcites →https://doi.org/10.1016/j.bmcl.2006.02.018openalex-snapshot
N-Benzylbenzamides: A new class of potent tyrosinase inhibitors
inferredcites →https://doi.org/10.1016/j.bmcl.2006.08.018openalex-snapshot
Chemical transformations of oxyresveratrol (trans-2,4,3′,5′-tetrahydroxystilbene) into a potent tyrosinase inhibitor and a strong cytotoxic agent
inferredcites →https://doi.org/10.1016/j.bmcl.2006.10.025openalex-snapshot
Syntheses of hydroxy substituted 2-phenyl-naphthalenes as inhibitors of tyrosinase
inferredcites →https://doi.org/10.1016/j.bmcl.2008.08.053openalex-snapshot
Molecular design of potent tyrosinase inhibitors having the bibenzyl skeleton
inferredcites →https://doi.org/10.1016/j.bmcl.2011.09.130openalex-snapshot
Evaluation of new chalcone derivatives as polyphenol oxidase inhibitors
inferredcites →https://doi.org/10.1016/j.chembiol.2004.02.014openalex-snapshot
A New Class of Phytoestrogens
inferredcites →https://doi.org/10.1016/j.jmb.2010.10.048openalex-snapshot
First Structures of an Active Bacterial Tyrosinase Reveal Copper Plasticity
inferredcites →https://doi.org/10.1016/s0308-8146(02)00418-1openalex-snapshot
Molecular design of antibrowning agents: antioxidative tyrosinase inhibitors
inferredcites →https://doi.org/10.1021/bi200395topenalex-snapshot
Crystal Structure of Agaricus bisporus Mushroom Tyrosinase: Identity of the Tetramer Subunits and Interaction with Tropolone
inferredcites →https://doi.org/10.1021/jf072893lopenalex-snapshot
Identification of Geranic Acid, a Tyrosinase Inhibitor in Lemongrass (Cymbopogon citratus)
inferredcites →https://doi.org/10.1034/j.1600-0749.2003.00084.xopenalex-snapshot
Down‐Regulation of Melanin Synthesis by a Biphenyl Derivative and Its Mechanism
inferredcites →https://doi.org/10.1248/bpb.28.323openalex-snapshot
4,4′-Dihydroxybiphenyl as a New Potent Tyrosinase Inhibitor
inferredcites →https://doi.org/10.1248/cpb.51.318openalex-snapshot
A New Stilbene with Tyrosinase Inhibitory Activity from Chlorophora excelsa.
inferredcites →https://doi.org/10.3390/ijms10062440openalex-snapshot
An Updated Review of Tyrosinase Inhibitors
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Kinetic Studies, Molecular Docking, and Antioxidant Activity of Novel 1,3-Diphenyl Pyrazole Derivatives Coupled with Thiosemicarbazide with Anti-Tyrosinase and Anti-Melanogenesis Properties
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Enantioselective Synthesis of Isoflavanones and Pterocarpans through a RuII‐Catalyzed ATH‐DKR of Isoflavones
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Cover Feature: Enantioselective Synthesis of Isoflavanones and Pterocarpans through a RuII‐Catalyzed ATH‐DKR of Isoflavones (ChemCatChem 24/2021)
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Tyrosinase Inhibition and Antimelanogenic Effects of Resorcinol‐Containing Compounds
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Withania somnifera Extract/Withaferin A as a Prospective Anti-pigmenting Agent
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Withaferin A abolishes the stem cell factor-stimulated pigmentation of human epidermal equivalents by interrupting the auto-phosphorylation of c-KIT in human melanocytes
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Novel 1,2,4-triazole analogues as mushroom tyrosinase inhibitors: synthesis, kinetic mechanism, cytotoxicity and computational studies
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Synthesis, structural elucidation and bioevaluation of 4-amino-1,2,4-triazole-3-thione’s Schiff base derivatives
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In silico ADMET, molecular docking and molecular simulation-based study of glabridin’s natural and semisynthetic derivatives as potential tyrosinase inhibitors
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Isobenzofuran-1(3H)-ones as new tyrosinase inhibitors: Biological activity and interaction studies by molecular docking and NMR
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Molecular modeling and phenoloxidase inhibitory activity of arbutin and arbutin undecylenic acid ester
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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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Synthesis, in vitro, and in silico study of novel pyridine based 1,3-diphenylurea derivatives as tyrosinase inhibitors
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Antioxidant, anti-tyrosinase and anti-melanogenic effects of (E)-2,3-diphenylacrylic acid derivatives
inferred← citeshttps://doi.org/10.1016/j.bmcl.2019.07.055openalex-snapshot
Synthesis of N-arylindazole-3-carboxamide and N-benzoylindazole derivatives and their evaluation against α-MSH-stimulated melanogenesis
inferred← citeshttps://doi.org/10.1016/j.cellsig.2017.09.004openalex-snapshot
Recent development of signaling pathways inhibitors of melanogenesis
inferred← citeshttps://doi.org/10.1016/j.cyto.2015.02.006openalex-snapshot
Astaxanthin and withaferin A block paracrine cytokine interactions between UVB-exposed human keratinocytes and human melanocytes via the attenuation of endothelin-1 secretion and its downstream intracellular signaling
inferred← citeshttps://doi.org/10.1016/j.drudis.2016.09.016openalex-snapshot
Downregulation of melanogenesis: drug discovery and therapeutic options
inferred← citeshttps://doi.org/10.1016/j.ejmech.2020.112275openalex-snapshot
A medicinal chemistry perspective of drug repositioning: Recent advances and challenges in drug discovery
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2016.01.070openalex-snapshot
4-Hydroxy cinnamic acid as mushroom preservation: Anti-tyrosinase activity kinetics and application
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Facile synthesis of new quinazolinone benzamides as potent tyrosinase inhibitors: Comparative spectroscopic and molecular docking studies
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Design, synthesis, biological evaluation, and molecular docking study of thioxo-2,3-dihydroquinazolinone derivative as tyrosinase inhibitors
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Ensemble-Based Virtual Screening Led to the Discovery of New Classes of Potent Tyrosinase Inhibitors
inferred← citeshttps://doi.org/10.1021/acs.jmedchem.7b00967openalex-snapshot
Inhibitors of Melanogenesis: An Updated Review
inferred← citeshttps://doi.org/10.1021/acs.orglett.6b00643openalex-snapshot
Exploiting Aryl Mesylates and Tosylates in Catalytic Mono-α-arylation of Aryl- and Heteroarylketones
inferred← citeshttps://doi.org/10.1039/d5ra05084gopenalex-snapshot
7-Methoxybenzofuran-triazole tethered N -phenylacetamides as a promising class of tyrosinase inhibitors: synthesis, biological evaluation and computational analyses against fungal and human tyrosinases
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/10.1080/1062936x.2020.1862297openalex-snapshot
SAR and QSAR research on tyrosinase inhibitors using machine learning methods
inferred← citeshttps://doi.org/10.1080/14756366.2016.1256882openalex-snapshot
Skin whitening agents: medicinal chemistry perspective of tyrosinase inhibitors
inferred← citeshttps://doi.org/10.1155/2015/262364openalex-snapshot
Estimation of Inhibitory Effect against Tyrosinase Activity through Homology Modeling and Molecular Docking
inferred← citeshttps://doi.org/10.1517/17460441.2014.907789openalex-snapshot
Design and discovery of mushroom tyrosinase inhibitors and their therapeutic applications
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Development of Stilbenoid and Chalconoid Analogues as Potent Tyrosinase Modulators and Antioxidant Agents
inferred← citeshttps://doi.org/10.3390/antiox13101248openalex-snapshot
Design, Synthesis, and Anti-Melanogenic Activity of 2-Mercaptomethylbenzo[d]imidazole Derivatives Serving as Tyrosinase Inhibitors: An In Silico, In Vitro, and In Vivo Exploration
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Jeju Magma-Seawater Inhibits α-MSH-Induced Melanogenesis via CaMKKβ-AMPK Signaling Pathways in B16F10 Melanoma Cells
inferred← citeshttps://doi.org/10.3390/molecules21091230openalex-snapshot
Combinatorial Synthesis of Structurally Diverse Triazole-Bridged Flavonoid Dimers and Trimers
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Anti-Melanogenic Properties of Greek Plants. A Novel Depigmenting Agent from Morus alba Wood
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Anti-Melanogenic Potential of Natural and Synthetic Substances: Application in Zebrafish Model
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Identification by shape-based virtual screening and evaluation of new tyrosinase inhibitors
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