NATURAL PRODUCT RESEARCH AND DEVELOPMENT ›› 2025, Vol. 37 ›› Issue (1): 57-64. doi: 10.16333/j.1001-6880.2025.1.007 cstr: 32307.14.1001-6880.2025.1.007

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Chemical constituents from the ethyl acetate extract of Lycium barbarum L. fruits and their biological activities

SHANG Ying1,ZHU Yi-dong1,ZHANG Hui1,JIANG Zhi-bo1,2,3,MA Xiao-li1,2,3,NAN Ze-dong1,2,3 *   

  1. 1School of Chemistry and Chemical Engineering,North Minzu University;2Ningxia Key Laboratory of Solar Chemical Conversion Technology;3Key Laboratory for Chemical Engineering and Technology,State Ethnic Affairs Commission,Yinchuan 750021,China
  • Online:2025-01-22 Published:2025-01-22

Abstract:

To investigate the chemical constituents and biological activities from the fruits of Lycium barbarum L.,seventeen compounds were isolated and purified from the ethyl acetate extract of 75% ethanol extract of fruits of L. barbarum by using various chromatographic methods,their structures were elucidated via NMR,MS techniques as:oxypeucedanin hydrate (1),pangelin (2),byakangelicol (3),phellopterin (4),3-[2-formyl-5-(hydroxymethyl)-1H-pyrrol-1-yl] pentanedioic acid (5),4-[2-formyl-5-(hydroxymethyl)-1H-pyrrol-1-yl]butanoic acid (6),3-methoxyl-1H-pyrrole (7),nicotiamide (8),5-hydroxyl-2-hydroxymethylpyridine (9),5-hydroxymethyl-furaldehyde (10),stigmast-4-en-3-one (11),(+)-hannokinol (12),trans-ferulic acid (13),4-hydroxycinnamic acid (14),2,4-dimethoxy-2-methyl-(6H)-pyran-3-one (15),4-hydroxybenzaldehyde (16),p-hydroxybenzoic acid (17).Among these compounds,1-4 were isolated from Lycium genus for the first time,and 11 was isolated from L. barbarum for the first time.The biological activities were investigated through DPPH radical scavenging and tyrosinase-catalyzed L-dopa oxidation effects.The results indicated that compounds 1,4,5,12,14 and 15 showed potent scavenging ability on DPPH free radical with IC50 values ranging from 0.17 μg/mL to 87.56 μg/mL,and 3-9,11,14 and 17 exhibited good inhibition on tyrosinase with IC50 values range of 1.65-68.76 μg/mL.Among them,the antioxidant capacity of 5 and 14 was better than the positive control ascorbic acid,and the inhibitory capacity of 3,6,8 and 11 was higher than arbutin(positive control).

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