In the course of screening for the melanogenesis inhibitors, rengyolone was isolated from Eurya emarginata (Thumb) Makino. Its chemical structure was determined on the basis of spectroscopic analysis including mass spectroscopy and nuclear magnetic resonance analysis. Rengyolone inhibited potent melanogenesis in melan-a cells with an IC50 value of 65 μM without cytotoxicity. Also, rengyolone showed a melanin biosynthesis inhibition zone in a culture plate of Streptomyces bikiniensis, which is commonly used as an indicator organism. Moreover, rengyolone dramatically reduced protein expression of melanogenic enzyme, tyrosinase. Furthermore, rengyolone presented inhibition on the body pigmentation in zebrafish model system and decreased melanin contents and tyrosinase activity. These results suggest that rengyolone isolated from E. emarginata may be an effective skin-whitening agent that regulates the expression of melanogenic enzymes.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1002/ptr.5082 | DOI Listing |
Nat Prod Res
January 2024
Department of Chemistry, Faculty of Science, Silpakorn University, Nakhon Pathom, Thailand.
In this study, a new acylated triterpene glycoside, 3--stearoyl-28-[2'-stearoyl--l-arabinopyranosyl]-olean-12-en-28-oic acid (), was isolated from the flowers of . In addition to this compound, eleven known compounds were also isolated, including a related pentacyclic triterpenoid: ursolic acid (), two cycloartane triterpenoids: 24-methylenecycloartanol () and 24-methylenecycloartane-3,28-diol (), three cyclohexylethane derivatives: (-)-rengyolone (), (-)-cleroindicin C () and (-)-cleroindicin D (), an iridoid: 6---feruloyl catalpol (), two phenylethanoid glycosides: salidroside () and verbascoside (), and two steroids: -sitosterol () and -sitosterol-3---d-glucopyranoside (). The chemical structures of these compounds were determined by analysing their HRMS and NMR spectroscopic data.
View Article and Find Full Text PDFChemistry
June 2022
Department of Chemistry and, FQRNT Centre for Green Chemistry and Catalysis, McGill University, 801 Sherbrooke St. W., Montreal, Quebec, H3A 0B8, Canada.
The synthesis of arylamines from renewable resources under mild reaction conditions is highly desired for the sustainability of the chemical industry, where the production of hazardous waste is a prime concern. However, to date, there are very few tools in chemists' toolboxes that are able to produce arylamines in a sustainable manner. Herein, a robust one-pot approach for constructing bio-based arylamines via a combined photooxidative dearomatization-rearomatization strategy is presented.
View Article and Find Full Text PDFDolichandrone serrulata (DC.) Seem flowers are widely used as vegetables in northern and eastern Thailand. Biological studies of the methanolic extract of these flowers have shown promising antioxidant activity.
View Article and Find Full Text PDFPhytother Res
June 2014
Department of Herbal Skin Care, Daegu Haany University, Gyeongsan, Gyeongbuk, 712-715, Korea.
In the course of screening for the melanogenesis inhibitors, rengyolone was isolated from Eurya emarginata (Thumb) Makino. Its chemical structure was determined on the basis of spectroscopic analysis including mass spectroscopy and nuclear magnetic resonance analysis. Rengyolone inhibited potent melanogenesis in melan-a cells with an IC50 value of 65 μM without cytotoxicity.
View Article and Find Full Text PDFNat Prod Res
January 2014
Pharmacognosy Department, Faculty of Pharmacy, Beni-Suef University, Beni-Suef, Egypt.
Chloroformic and methanolic extracts of four Clerodendrum species cultivated in Egypt were screened for antimicrobial activities. Chloroformic extracts of the flowers of Clerodendrum chinense and Clerodendrum splendens were active against Plasmodium falciparum (IC50 < 10 µg mL(-1)). Chloroformic extracts of the stem and flowers of C.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!