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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

https://doi.org/10.2139/ssrn.4760920
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inferredcites →https://doi.org/10.1007/s00204-020-02689-3openalex-extracted
Antioxidants and antioxidant methods: an updated overview
inferredcites →https://doi.org/10.1007/s10311-021-01232-9openalex-extracted
Green synthesis of biologically active heterocycles of medicinal importance: a review
inferredcites →https://doi.org/10.1016/0378-4274(91)90074-gopenalex-extracted
Mutagenicity studies of kojic acid
inferredcites →https://doi.org/10.1016/j.bbrc.2011.08.094openalex-extracted
Role of metabolism by the human intestinal microflora in arbutin-induced cytotoxicity in HepG2 cell cultures
inferredcites →https://doi.org/10.1016/j.bioorg.2018.04.026openalex-extracted
Synthesis of aryl pyrazole via Suzuki coupling reaction, in vitro mushroom tyrosinase enzyme inhibition assay and in silico comparative molecular docking analysis with Kojic acid
inferredcites →https://doi.org/10.1016/j.bioorg.2018.09.003openalex-extracted
Inhibitory properties of aromatic thiosemicarbazones on mushroom tyrosinase: Synthesis, kinetic studies, molecular docking and effectiveness in melanogenesis inhibition
inferredcites →https://doi.org/10.1016/j.bioorg.2018.10.026openalex-extracted
Carbazole and hydrazone derivatives as new competitive inhibitors of tyrosinase: Experimental clues to binuclear copper active site binding
inferredcites →https://doi.org/10.1016/j.bioorg.2020.104108openalex-extracted
Coumaric acid derivatives as tyrosinase inhibitors: Efficacy studies through in silico, in vitro and ex vivo approaches
inferredcites →https://doi.org/10.1016/j.bioorg.2021.104979openalex-extracted
Anti-melanogenesis and anti-tyrosinase properties of aryl-substituted acetamides of phenoxy methyl triazole conjugated with thiosemicarbazide: Design, synthesis and biological evaluations
inferredcites →https://doi.org/10.1016/j.bmc.2005.03.012openalex-extracted
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.2006.05.014openalex-extracted
Oxazolones: New tyrosinase inhibitors; synthesis and their structure–activity relationships
inferredcites →https://doi.org/10.1016/j.bmc.2007.10.102openalex-extracted
1-(1-Arylethylidene)thiosemicarbazide derivatives: A new class of tyrosinase inhibitors
inferredcites →https://doi.org/10.1016/j.bmc.2010.06.046openalex-extracted
Synthesis of novel 3,5-diaryl pyrazole derivatives using combinatorial chemistry as inhibitors of tyrosinase as well as potent anticancer, anti-inflammatory agents
inferredcites →https://doi.org/10.1016/j.bmc.2012.07.001openalex-extracted
Synthesis, biological evaluation, and molecular docking of N-{3-[3-(9-methyl-9H-carbazol-3-yl)-acryloyl]-phenyl}-benzamide/amide derivatives as xanthine oxidase and tyrosinase inhibitors
inferredcites →https://doi.org/10.1016/j.bmc.2012.12.053openalex-extracted
Synthesis of new heterocyclic hybrids based on pyrazole and thiazolidinone scaffolds as potent inhibitors of tyrosinase
inferredcites →https://doi.org/10.1016/j.bmc.2012.12.054openalex-extracted
Design and synthesis of 3,5-diaryl-4,5-dihydro-1H-pyrazoles as new tyrosinase inhibitors
inferredcites →https://doi.org/10.1016/j.bmc.2014.04.060openalex-extracted
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inferredcites →https://doi.org/10.1016/j.bmc.2015.01.024openalex-extracted
Rational design, synthesis and structure–activity relationships of 4-alkoxy- and 4-acyloxy-phenylethylenethiosemicarbazone analogues as novel tyrosinase inhibitors
inferredcites →https://doi.org/10.1016/j.bmc.2019.04.020openalex-extracted
Antioxidant, anti-tyrosinase and anti-melanogenic effects of (E)-2,3-diphenylacrylic acid derivatives
inferredcites →https://doi.org/10.1016/j.bmc.2021.116044openalex-extracted
The natural-based optimization of kojic acid conjugated to different thio-quinazolinones as potential anti-melanogenesis agents with tyrosinase inhibitory activity
inferredcites →https://doi.org/10.1016/j.bmcl.2007.10.014openalex-extracted
Discovery of small-molecule inhibitors of tyrosinase
inferredcites →https://doi.org/10.1016/j.bmcl.2012.07.029openalex-extracted
Design, synthesis and molecular simulation studies of dihydrostilbene derivatives as potent tyrosinase inhibitors
inferredcites →https://doi.org/10.1016/j.bmcl.2017.05.057openalex-extracted
Thiosemicarbazones as inhibitors of tyrosinase enzyme
inferredcites →https://doi.org/10.1016/j.drudis.2016.09.016openalex-extracted
Downregulation of melanogenesis: drug discovery and therapeutic options
inferredcites →https://doi.org/10.1016/j.ejmech.2015.02.013openalex-extracted
Structure-based modification of 3-/4-aminoacetophenones giving a profound change of activity on tyrosinase: From potent activators to highly efficient inhibitors
inferredcites →https://doi.org/10.1016/j.ejmech.2016.04.077openalex-extracted
The therapeutic voyage of pyrazole and its analogs: A review
inferredcites →https://doi.org/10.1016/j.ejmech.2017.08.033openalex-extracted
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inferredcites →https://doi.org/10.1016/j.ejmech.2020.112480openalex-extracted
Kojic acid–natural product conjugates as mushroom tyrosinase inhibitors
inferredcites →https://doi.org/10.1016/j.ejmech.2021.113744openalex-extracted
Recent advances in the design and discovery of synthetic tyrosinase inhibitors
inferredcites →https://doi.org/10.1016/j.foodchem.2015.05.124openalex-extracted
Inhibitory effect of synthetic aromatic heterocycle thiosemicarbazone derivatives on mushroom tyrosinase: Insights from fluorescence, 1 H NMR titration and molecular docking studies
inferredcites →https://doi.org/10.1016/j.foodchem.2020.128232openalex-extracted
Effect directed synthesis of a new tyrosinase inhibitor with anti-browning activity
inferredcites →https://doi.org/10.1016/j.ijbiomac.2013.09.056openalex-extracted
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inferredcites →https://doi.org/10.1016/j.jmb.2010.10.048openalex-extracted
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Crystal Structure of Agaricus bisporus Mushroom Tyrosinase: Identity of the Tetramer Subunits and Interaction with Tropolone
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Natural and synthetic flavonoid derivatives as new potential tyrosinase inhibitors: a systematic review
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Crystallographic Evidence That the Dinuclear Copper Center of Tyrosinase Is Flexible during Catalysis
inferredcites →https://doi.org/10.1074/jbc.m709014200openalex-extracted
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inferredcites →https://doi.org/10.1093/carcin/23.6.1071openalex-extracted
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inferredcites →https://doi.org/10.1111/j.1471-4159.2005.03019.xopenalex-extracted
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inferredcites →https://doi.org/10.1111/j.1751-1097.2007.00226.xopenalex-extracted
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Naturally Available Nitrogen-Containing Fused Heterocyclics as Prospective Lead Molecules in Medicinal Chemistry
inferredcites →https://doi.org/10.3109/14756366.2015.1004058openalex-extracted
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inferredcites →https://doi.org/10.3389/fphar.2021.666725openalex-extracted
Heterocyclic Compounds: Pharmacology of Pyrazole Analogs From Rational Structural Considerations
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inferredcites →https://doi.org/10.3390/molecules14010519openalex-extracted
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inferredcites →https://doi.org/10.7831/ras.7.41openalex-extracted
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