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An Isoxazole Chalcone Derivative Enhances Melanogenesis in B16 Melanoma Cells via the Akt/GSK3β/β-Catenin Signaling Pathways.
- Source :
-
Molecules (Basel, Switzerland) [Molecules] 2017 Nov 28; Vol. 22 (12). Date of Electronic Publication: 2017 Nov 28. - Publication Year :
- 2017
-
Abstract
- Plants or plant-derived products have been routinely used in several traditional medicine systems for vitiligo treatment. It is well-known that melanogenesis can be promoted by certain flavonoid compounds isolated from the traditional Uyghur medicinal plant, Kaliziri. Therefore, Chalcones, one class of flavonoid compounds, has become an interesting target for the development of anti-vitiligo agents. A series of novel isoxazole chalcone derivatives have been designed, synthesized, and evaluated for biological activities by our group. Among them, derivative 1-(4-((3-phenylisoxazol-5-yl)methoxy)phenyl)-3-phenylprop-2-en-1-one (PMPP) was identified as a potent tyrosinase activator with better activity and lower toxicity than the positive control 8-methoxypsoralen (8-MOP) in this study. Further investigations revealed that Akt and GSK3β were the signaling pathways involved in the hyperpigmentation of PMPP. Overall, these studies may provide a convenient and novel approach for the further development of anti-vitiligo agents.<br />Competing Interests: All authors declare that there are no conflict of interest.
- Subjects :
- Animals
Chalcones chemistry
Gene Expression Regulation, Enzymologic drug effects
Melanoma, Experimental
Mice
Monophenol Monooxygenase metabolism
Plant Extracts chemistry
Chalcones pharmacology
Glycogen Synthase Kinase 3 beta metabolism
Melanins biosynthesis
Plant Extracts pharmacology
Proto-Oncogene Proteins c-akt metabolism
Signal Transduction drug effects
beta Catenin metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1420-3049
- Volume :
- 22
- Issue :
- 12
- Database :
- MEDLINE
- Journal :
- Molecules (Basel, Switzerland)
- Publication Type :
- Academic Journal
- Accession number :
- 29182558
- Full Text :
- https://doi.org/10.3390/molecules22122077