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New 4',5'-methylenedioxyflavone derivatives from the whole plant of sarcandra glabra.
Qin, Ya-Qiu; Liu, Wei; Yin, Rui; Xiao, Ping-Ting; Wang, Zi-Yuan; Huang, Tian-Qing; Liu, E-Hu.
Affiliation
  • Qin YQ; State Key Laboratory of Natural Medicines, China Pharmaceutical University, Nanjing, China.
  • Liu W; State Key Laboratory of Natural Medicines, China Pharmaceutical University, Nanjing, China.
  • Yin R; State Key Laboratory of Natural Medicines, China Pharmaceutical University, Nanjing, China.
  • Xiao PT; State Key Laboratory of Natural Medicines, China Pharmaceutical University, Nanjing, China.
  • Wang ZY; State Key Laboratory of Natural Medicines, China Pharmaceutical University, Nanjing, China.
  • Huang TQ; State Key Laboratory of Natural Medicines, China Pharmaceutical University, Nanjing, China.
  • Liu EH; State Key Laboratory of Natural Medicines, China Pharmaceutical University, Nanjing, China.
Nat Prod Res ; : 1-9, 2022 Aug 12.
Article in En | MEDLINE | ID: mdl-35959693
ABSTRACT
Two new natural products named 5,7-dihydroxy-3,3',6,8-tetramethoxy-4',5'-methylenedioxyflavone (1) and 3,3',5,7-tetramethoxy-4',5'-methylenedioxyflavone (2), along with thirteen known compounds, ß-sitosterol (3), desmethoxyyangonin (4), hexadecane (5), 3,9-bis(2,4-di-tert-butylphenoxy)-2,4,8,10-tetraoxa-3,9-diphosphaspiro [5.5] undecane 3,9-dioxide (6), 2'6'-dihydroxy-4'-methoxydihydrochalcone (7), cardamonin (8), 3,3',5,6,7,8-hexamethoxy-4',5'-methylenedioxyflavone (9), isofraxidin (10), aniba dimer A (11), 3,3',4',5,5',8-hexamethoxy-6,7-methylenedioxyflavone (12), quercetin (13), quercitrin (14) and isoquercitrin (15) were isolated from Sarcandra glabra (Thunb.) Nakai by various chromatographic methods. Compounds 1, 2, 4, 6, 11, and 12 were isolated from S. glabra for the first time. Their chemical structures were identified through the analysis of NMR and HR-MS spectra. The anti-inflammatory and cytotoxic activities of compounds 1-15 were evaluated in cell assays. The results indicated that compounds 1, 7, 8, 10, 14, and 15 significantly inhibited the NO production in LPS-induced RAW 264.7 murine macrophage cells. Moreover, compounds 1, 3, 4, 7, 8, 9, 10 and 12 exhibited a cytotoxic effect on the human HepG2 cell line.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Nat Prod Res Year: 2022 Document type: Article Affiliation country: China

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Nat Prod Res Year: 2022 Document type: Article Affiliation country: China