Two new quinochalcone glycosides, hydroxysafflor yellow A-4'---D-glucopyranoside () and 3'-hydroxyhydroxysafflor yellow A (), were isolated from the safflower yellow pigments of . The structures of new compounds were elucidated by a detailed spectroscopic analysis (UV, IR, HR-ESI-MS, 1D and 2D NMR, ECD). The assay indicated that compound could improve the survived rate of primary mouse cortical neurons on glutamate-induced neurons damage model at a concentration of 10 μM.
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http://dx.doi.org/10.1080/10286020.2020.1846530 | DOI Listing |
Phytochemistry
June 2024
State Key Laboratory of Bioactive Substance and Function of Natural Medicines, Institute of Materia Medica, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100050, China. Electronic address:
Safflopentsides A-C (1-3), three highly oxidized rearranged derivatives of quinochalcone C-glycosides, were isolated from the safflower yellow pigments. Their structures were determined based on a detailed spectroscopic analysis (UV, IR, HR-ESI-MS, 1D and 2D NMR), and the absolute configurations were confirmed by the comparison of experimental ECD spectra with calculated ECD spectra. Compounds 1-3 have an unprecedented cyclopentenone or cyclobutenolide ring A containing C-glucosyl group, respectively.
View Article and Find Full Text PDFJ Asian Nat Prod Res
May 2024
Chemistry Department, Faculty of Science, Jazan University, Jazan 2097, Kingdom of Saudi Arabia.
A new quinochalcone -glycoside featuring a unique quinonoid moiety, named celochalcoside (), was isolated from the -butanol extract of the aerial parts of L. The structure was determined by extensive spectroscopic analysis as well as mass spectrometric data. Compound showed moderate cytotoxic activities against breast cancer cell lines (MCF-7), colon cancer cell lines (HT-29) and hepatocellular carcinoma cell lines (HepG2) with IC values of 23.
View Article and Find Full Text PDFJ Am Soc Mass Spectrom
October 2021
Military University of Technology, Institute of Chemistry, Gen. S. Kaliskiego 2, 00-908 Warsaw, Poland.
Safflower ( L.) petals, depending on the nature of a dyeing bath, dye fibers yellow or red. This is due to the presence of two kinds of components, water-soluble yellow colorants and alkali-soluble red compounds.
View Article and Find Full Text PDFPlant Cell Physiol
December 2021
Department of Biomolecular Engineering, Graduate School of Engineering, Tohoku University, Aza Aoba, Aramaki, Aoba 6-6-11, Sendai, Miyagi 980-8579, Japan.
Carthamin, a dimeric quinochalcone that is sparingly soluble in water, is obtained from the yellow-orange corolla of fully blooming safflower (Carthamus tinctorius L.) florets. Carthamin is a natural red colorant, which has been used worldwide for more than 4500 years and is the major component of Japanese 'beni' used for dyeing textiles, in cosmetics and as a food colorant.
View Article and Find Full Text PDFJ Asian Nat Prod Res
December 2020
State Key Laboratory of Bioactive Substance and Function of Natural Medicines, Institute of Materia Medica, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100050, China.
Two new quinochalcone glycosides, hydroxysafflor yellow A-4'---D-glucopyranoside () and 3'-hydroxyhydroxysafflor yellow A (), were isolated from the safflower yellow pigments of . The structures of new compounds were elucidated by a detailed spectroscopic analysis (UV, IR, HR-ESI-MS, 1D and 2D NMR, ECD). The assay indicated that compound could improve the survived rate of primary mouse cortical neurons on glutamate-induced neurons damage model at a concentration of 10 μM.
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