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Design, Synthesis, Structural Insights, Tyrosinase Inhibition, and Sun Protection Factor of New Thiosemicarbazone Derivatives
by
Masuri, Sebastiano
, Era, Benedetta
, Cabiddu, Maria Grazia
, Fais, Antonella
, Pintus, Francesca
, Pettinau, Francesca
, Meloni, Francesca
, Podda, Enrico
, Floris, Sonia
, Pivetta, Tiziana
in
Agaricales - enzymology
/ Copper
/ Crystal structure
/ Cytotoxicity
/ Drug Design
/ enzyme inhibition
/ Enzyme Inhibitors - chemical synthesis
/ Enzyme Inhibitors - chemistry
/ Enzyme Inhibitors - pharmacology
/ Enzymes
/ Evaluation
/ Humans
/ Hydrogen
/ Molecular Docking Simulation
/ Molecular Structure
/ Monophenol Monooxygenase - antagonists & inhibitors
/ Monophenol Monooxygenase - metabolism
/ Physiological aspects
/ Structure-Activity Relationship
/ Sun Protection Factor
/ Sunscreening Agents - chemical synthesis
/ Sunscreening Agents - chemistry
/ Sunscreening Agents - pharmacology
/ thiosemicarbazones
/ Thiosemicarbazones - chemical synthesis
/ Thiosemicarbazones - chemistry
/ Thiosemicarbazones - pharmacology
/ tyrosinase
2024
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Design, Synthesis, Structural Insights, Tyrosinase Inhibition, and Sun Protection Factor of New Thiosemicarbazone Derivatives
by
Masuri, Sebastiano
, Era, Benedetta
, Cabiddu, Maria Grazia
, Fais, Antonella
, Pintus, Francesca
, Pettinau, Francesca
, Meloni, Francesca
, Podda, Enrico
, Floris, Sonia
, Pivetta, Tiziana
in
Agaricales - enzymology
/ Copper
/ Crystal structure
/ Cytotoxicity
/ Drug Design
/ enzyme inhibition
/ Enzyme Inhibitors - chemical synthesis
/ Enzyme Inhibitors - chemistry
/ Enzyme Inhibitors - pharmacology
/ Enzymes
/ Evaluation
/ Humans
/ Hydrogen
/ Molecular Docking Simulation
/ Molecular Structure
/ Monophenol Monooxygenase - antagonists & inhibitors
/ Monophenol Monooxygenase - metabolism
/ Physiological aspects
/ Structure-Activity Relationship
/ Sun Protection Factor
/ Sunscreening Agents - chemical synthesis
/ Sunscreening Agents - chemistry
/ Sunscreening Agents - pharmacology
/ thiosemicarbazones
/ Thiosemicarbazones - chemical synthesis
/ Thiosemicarbazones - chemistry
/ Thiosemicarbazones - pharmacology
/ tyrosinase
2024
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Design, Synthesis, Structural Insights, Tyrosinase Inhibition, and Sun Protection Factor of New Thiosemicarbazone Derivatives
by
Masuri, Sebastiano
, Era, Benedetta
, Cabiddu, Maria Grazia
, Fais, Antonella
, Pintus, Francesca
, Pettinau, Francesca
, Meloni, Francesca
, Podda, Enrico
, Floris, Sonia
, Pivetta, Tiziana
in
Agaricales - enzymology
/ Copper
/ Crystal structure
/ Cytotoxicity
/ Drug Design
/ enzyme inhibition
/ Enzyme Inhibitors - chemical synthesis
/ Enzyme Inhibitors - chemistry
/ Enzyme Inhibitors - pharmacology
/ Enzymes
/ Evaluation
/ Humans
/ Hydrogen
/ Molecular Docking Simulation
/ Molecular Structure
/ Monophenol Monooxygenase - antagonists & inhibitors
/ Monophenol Monooxygenase - metabolism
/ Physiological aspects
/ Structure-Activity Relationship
/ Sun Protection Factor
/ Sunscreening Agents - chemical synthesis
/ Sunscreening Agents - chemistry
/ Sunscreening Agents - pharmacology
/ thiosemicarbazones
/ Thiosemicarbazones - chemical synthesis
/ Thiosemicarbazones - chemistry
/ Thiosemicarbazones - pharmacology
/ tyrosinase
2024
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Design, Synthesis, Structural Insights, Tyrosinase Inhibition, and Sun Protection Factor of New Thiosemicarbazone Derivatives
Journal Article
Design, Synthesis, Structural Insights, Tyrosinase Inhibition, and Sun Protection Factor of New Thiosemicarbazone Derivatives
2024
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Overview
Tyrosinase, a key protein in the biosynthesis of melanin pigments, is crucial in determining skin pigmentation. Inhibiting tyrosinase activity is a promising approach for treating conditions related to excessive pigmentation. For the synthesis of more potent tyrosinase inhibitors, we combined two approaches, para-substitution and lipophilicity, to enhance the inhibitory properties of (E)-2-(4-hydroxybenzylidene)hydrazine-1-carbotiamide, whose enzyme inhibitory properties have been previously demonstrated. The newly synthesized compounds showed potent inhibition activity against tyrosinase in the micromolar concentration range. The synthesised compounds were up to 41 times more effective than kojic acid. In addition to this biological activity, all molecules were evaluated for their sun protection factor to determine their photoprotective effects. All the compounds showed higher efficacy than reference compounds, used as sunscreens in photoprotective preparations. All compounds were noncytotoxic at the concentration required to inhibit tyrosinase activity. With the aim of defining the potential binding modes and the kind of interactions between the studied molecules and the catalytic site of mushroom tyrosinase, molecular docking simulations were also performed.
Publisher
MDPI AG,MDPI
Subject
/ Copper
/ Enzyme Inhibitors - chemical synthesis
/ Enzyme Inhibitors - chemistry
/ Enzyme Inhibitors - pharmacology
/ Enzymes
/ Humans
/ Hydrogen
/ Molecular Docking Simulation
/ Monophenol Monooxygenase - antagonists & inhibitors
/ Monophenol Monooxygenase - metabolism
/ Structure-Activity Relationship
/ Sunscreening Agents - chemical synthesis
/ Sunscreening Agents - chemistry
/ Sunscreening Agents - pharmacology
/ Thiosemicarbazones - chemical synthesis
/ Thiosemicarbazones - chemistry
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