An examination of natural and synthetic tyrosinase inhibitors DOI Open Access
Gizem Demirdiş

European Journal of Life Sciences, Год журнала: 2024, Номер 3(3), С. 114 - 126

Опубликована: Дек. 31, 2024

The enzyme responsible for this process is known as tyrosinase, which sometimes referred to polyphenol oxidase, monophenol phenolase, or catecholase. It present in humans, plants, microbes, and fungi. Melanin pigments, found both plants animals, require an essential component. Tyrosinase animal creatures, particularly the pigments of skin, hair, eyes. can cause darkening foods that unrelated their inherent color. Beverages such fruit juice wine may experience a decline appearance flavor, well occurrence turbidity precipitation. unwanted phenomenon browning fruits vegetables, frequently caused by enzymatic processes, needs be avoided. inhibitors are employed hinder catalytic oxidations lead tyrosinase enzyme. Currently, these basic ingredients commonly skin whitening solutions, field cosmetics. In addition, have practical applications treatment problems associated with melanin pigmentation. Furthermore, competitively reversibly activity human melanocyte hence impeding production melanin.Numerous substances possess ability tyrosinase. Ongoing studies being conducted on several derivatized compounds increase inhibition. This article explores inhibitory effects many compounds, including kojic acid, azelaic flavonoids, arbutin-deoxyarbutin, curcumin its derivatives, copper chelators,

Язык: Английский

Small-Molecule Tyrosinase Inhibitors for Treatment of Hyperpigmentation DOI Creative Commons

Xinhua Ni,

Xinyu Luo, Xiaoying Jiang

и другие.

Molecules, Год журнала: 2025, Номер 30(4), С. 788 - 788

Опубликована: Фев. 8, 2025

Increasing attention is being focused on skin health currently, especially the excessive deposition of melanin in skin. Tyrosinase, rate-limiting enzyme biosynthesis, a crucial synthesis. However, existing tyrosinase inhibitors pose some degree toxicity to humans. Therefore, development more efficient and low-toxicity urgently needed. This review briefly depicts biosynthesis process crystal structure catalytic mechanism tyrosinase. The latest research progress regarding small-molecule also reviewed. Moreover, structure-function relationships are analyzed summarized. expected provide new scientific insights enable researchers explore safer potent inhibitors.

Язык: Английский

Процитировано

0

Grafted modified chitosan/pullulan film loaded with essential oil/β-CD-MOFs for freshness preservation of peach DOI
Linyun Mou, Ya Lu, Jiale Ma

и другие.

International Journal of Biological Macromolecules, Год журнала: 2025, Номер 306, С. 141491 - 141491

Опубликована: Фев. 27, 2025

Язык: Английский

Процитировано

0

Biomedical applications of tyrosinases and tyrosinase inhibitors DOI
L Pisano,

Martina Turco,

Claudiu T. Supuran

и другие.

˜The œEnzymes, Год журнала: 2024, Номер unknown, С. 261 - 280

Опубликована: Янв. 1, 2024

Язык: Английский

Процитировано

2

Computational studies of tyrosinase inhibitors DOI
Alessandro Bonardi, Paola Gratteri

˜The œEnzymes, Год журнала: 2024, Номер unknown, С. 191 - 229

Опубликована: Янв. 1, 2024

Язык: Английский

Процитировано

1

Investigation of the Inhibitory Activity of β‐Arbutin and Its Analogues on Tyrosinase Based on Molecular Docking and Enzyme Inhibition Kinetics DOI

Yuxiu Lv,

Chuanhui Yao,

Kangjia Han

и другие.

Chemistry & Biodiversity, Год журнала: 2024, Номер unknown

Опубликована: Окт. 7, 2024

β-Arbutin, a natural glucoside hydroquinone derivative known for its skin-whitening properties through tyrosinase inhibition in melanin synthesis, may pose potential risks of allergy and carcinogenicity due to the release during use. This study explores inhibitory effects phenyl-β-D-pyranoglucoside (compound 1), 4-methoxyphenyl-β-D-pyranoglucoside 2), 4-hydroxymethylphenyl-β-D-pyranoglucoside 3), β-arbutin 4) on using enzyme kinetics, molecular docking, dynamics simulations. Results show compounds 1, 3, 4 exhibit competitive inhibition, while compound 2 shows mixed inhibition. Docking analysis reveals phenyl rings all interact with enzyme's active site, 3 forming metal bond copper ions. MD simulations indicate high stability 2, 4, showing lowest RMSD compact Rg, suggesting stronger binding. Compound 1 is less stable inhibitory. These insights are valuable designing effective inhibitors.

Язык: Английский

Процитировано

1

An examination of natural and synthetic tyrosinase inhibitors DOI Open Access
Gizem Demirdiş

European Journal of Life Sciences, Год журнала: 2024, Номер 3(3), С. 114 - 126

Опубликована: Дек. 31, 2024

The enzyme responsible for this process is known as tyrosinase, which sometimes referred to polyphenol oxidase, monophenol phenolase, or catecholase. It present in humans, plants, microbes, and fungi. Melanin pigments, found both plants animals, require an essential component. Tyrosinase animal creatures, particularly the pigments of skin, hair, eyes. can cause darkening foods that unrelated their inherent color. Beverages such fruit juice wine may experience a decline appearance flavor, well occurrence turbidity precipitation. unwanted phenomenon browning fruits vegetables, frequently caused by enzymatic processes, needs be avoided. inhibitors are employed hinder catalytic oxidations lead tyrosinase enzyme. Currently, these basic ingredients commonly skin whitening solutions, field cosmetics. In addition, have practical applications treatment problems associated with melanin pigmentation. Furthermore, competitively reversibly activity human melanocyte hence impeding production melanin.Numerous substances possess ability tyrosinase. Ongoing studies being conducted on several derivatized compounds increase inhibition. This article explores inhibitory effects many compounds, including kojic acid, azelaic flavonoids, arbutin-deoxyarbutin, curcumin its derivatives, copper chelators,

Язык: Английский

Процитировано

0