Melanin pigmentation control by 1,3-thiazolidines: does NO scavenging play a critical role?
Author:
Affiliation:
1. Department of Chemical Sciences; University of Naples “Federico II”; Naples Italy
2. Department of Clinical Medicine and Surgery; University of Naples “Federico II”; Naples Italy
Publisher
Wiley
Subject
Dermatology,Molecular Biology,Biochemistry
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/exd.13033/fullpdf
Reference9 articles.
1. Hypopigmenting agents: an updated review on biological, chemical and clinical aspects
2. Different effects of five depigmentary compounds, rhododendrol, raspberry ketone, monobenzone, rucinol and AP736 on melanogenesis and viability of human epidermal melanocytes
3. A convenient screening method to differentiate phenolic skin whitening tyrosinase inhibitors from leukoderma-inducing phenols
4. 2-Aryl-1,3-thiazolodines as masked sulfhydryl agents for inhibition of melanogenesis
5. Design, synthesis and biological evaluation of 2-(substituted phenyl)thiazolidine-4-carboxylic acid derivatives as novel tyrosinase inhibitors
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1. Introducing a potential lead structure for the synthesis of more specific inhibitors of tyrosinases and catechol oxidases;Journal of the Iranian Chemical Society;2021-09-20
2. Natural and Bioinspired Phenolic Compounds as Tyrosinase Inhibitors for the Treatment of Skin Hyperpigmentation: Recent Advances;Cosmetics;2019-10-01
3. Vanillic acid in Panax ginseng root extract inhibits melanogenesis in B16F10 cells via inhibition of the NO/PKG signaling pathway;Bioscience, Biotechnology, and Biochemistry;2019-07-03
4. Hypopigmenting Effects of Brown Algae-Derived Phytochemicals: A Review on Molecular Mechanisms;Marine Drugs;2017-09-24
5. Design, synthesis, and antimelanogenic effects of (2-substituted phenyl-1,3-dithiolan-4-yl)methanol derivatives;Drug Design, Development and Therapy;2017-03
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