4H-benzochromene derivatives as novel tyrosinase inhibitors and radical scavengers: synthesis, biological evaluation, and molecular docking analysis-Reference-Cited by-同舟云学术

4H-benzochromene derivatives as novel tyrosinase inhibitors and radical scavengers: synthesis, biological evaluation, and molecular docking analysis

Published:2020-07-18 Issue:4 Volume:25 Page:2339-2349
ISSN:1381-1991
Container-title:Molecular Diversity
language:en
Short-container-title:Mol Divers

Author:

Karimian Somaye,Ranjbar Sara,Dadfar Mahsa,Khoshneviszadeh Mahsima,Gholampour Maryam,Sakhteman Amirhossein,Khoshneviszadeh Mehdi

Funder

Vice-Chancellor for Research, Shiraz University of Medical Sciences

Publisher

Springer Science and Business Media LLC

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Drug Discovery,Molecular Biology,General Medicine,Information Systems,Catalysis

Link

https://link.springer.com/content/pdf/10.1007/s11030-020-10123-0.pdf

Reference35 articles.

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3. Masum MN, Yamauchi K, Mitsunaga T (2019) Tyrosinase inhibitors from natural and synthetic sources as skin-lightening agents. Rev Agric Sci 7:41–58

4. Greggio E, Bergantino E, Carter D, Ahmad R, Costin GE et al (2005) Tyrosinase exacerbates dopamine toxicity but is not genetically associated with Parkinson’s disease. J Neurochem 93:246–256

5. Carballo-Carbajal I, Laguna A, Romero-Giménez J, Cuadros T, Bové J et al (2019) Brain tyrosinase overexpression implicates age-dependent neuromelanin production in Parkinson’s disease pathogenesis. Nat Commun 10:973

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