Bioactive prenylated c6-c3 derivatives from the roots of Illicium brevistylum

被引:1
|
作者
Zhang, Jing-Yu [1 ]
Yang, Hui-Lin [2 ]
Li, Wen-Rui [1 ]
Gao, Rong-Mei [3 ]
Li, Mi [1 ]
Wang, Ru-Bing [1 ]
Yang, Jia [1 ]
Wang, Qian-Ru [1 ]
Li, Yu-Huan [3 ]
Li, Li [2 ]
Ma, Shuang-Gang [1 ]
机构
[1] Chinese Acad Med Sci & Peking Union Med Coll, State Key Lab Bioact Subst & Funct Nat Med, Inst Mat Med, Beijing 100050, Peoples R China
[2] Chinese Acad Med Sci & Peking Union Med Coll, Inst Mat Med, Beijing Key Lab Drug Targets Identificat & Drug Sc, Beijing 100050, Peoples R China
[3] Chinese Acad Med Sci & Peking Union Med Coll, Peking Union Med Coll, Inst Med Biotechnol, Beijing 100050, Peoples R China
基金
中国国家自然科学基金;
关键词
Illicium brevistylum; roots; prenylated C-6-C-3 derivatives; anti-inflammatory activity; anti-Coxsackievirus B3; anti-influenza virus A; C-6-C-3; COMPOUNDS; CONSTITUENTS;
D O I
10.1080/10286020.2024.2365437
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Three new prenylated C-6-C-3 compounds (1-3), together with two known prenylated C-6-C-3 compounds (4-5) and one known C-6-C-3 derivative (6), were isolated from the roots of Illicium brevistylum A. C. Smith. The structures of 1-3 were elucidated by spectroscopic methods including 1D and 2D NMR, HRESIMS, CD experiments and ECD calculations. The structure of illibrefunone A (1) was confirmed by single-crystal X-ray diffraction analysis. All compounds were evaluated in terms of their anti-inflammatory potential on nitric oxide (NO) generation in lipopolysaccharide-stimulated murine RAW264.7 macrophages and murine BV2 microglial cells, antiviral activity against Coxsackievirus B3 (CVB3) and influenza virus A/Hanfang/359/95 (H3N2). Compounds 3 and 4 exhibited potent inhibitory effects on the production of NO in RAW 264.7 cells with IC50 values of 20.57 and 12.87 mu M respectively, which were greater than those of dexamethasone (positive control). Compounds 1 and 4-6 exhibited weak activity against Coxsackievirus B3, with IC50 values ranging from 25.87 to 33.33 mu M.
引用
收藏
页数:13
相关论文
共 50 条
  • [41] First synthesis of (±)-C-3-prenylated flavanones
    Xu, J
    Wang, HS
    Sim, MM
    SYNTHETIC COMMUNICATIONS, 2003, 33 (15) : 2737 - 2750
  • [42] ETUDE DE LINCORPORATION DUNITES C6-C3 DANS LES COMPOSES FLAVONIQUES CHEZ LE DIFFERENTS VEGETAUX ET SIGNIFICATION BIOGENETIQUE
    VILLE, A
    BULLETIN DE LA SOCIETE CHIMIQUE DE FRANCE, 1966, (02): : 488 - &
  • [43] C-13 NMR-SPECTRA OF SOME C-3 PRENYLATED COUMARINS FROM RUTACEAE
    BERGENTHAL, D
    SZENDREI, K
    REISCH, J
    ARCHIV DER PHARMAZIE, 1977, 310 (05) : 390 - 393
  • [44] C6-C3芳烃在HZSM-5,PHZSM-5及REY上吸附的红外研究
    郭文珪
    梁娟
    应慕良
    赵素琴
    胡皆汉
    郑海洋
    Chinese Journal of Catalysis, 1989, (04) : 402 - 408
  • [45] C-PRENYLATED AND O-PRENYLATED CHALCONES FROM CORDOA-PIACA
    DELIMA, OG
    MARINIBE.GB
    DEMELLO, JF
    DELLEMON.F
    DEBARROS.JS
    DEANDRAD.FD
    DEALBUQU.MM
    GAZZETTA CHIMICA ITALIANA, 1973, 103 (6-7): : 771 - 777
  • [46] C-prenylated dihydroflavonol from Rhynchosia densiflora
    Rao, KV
    Gunasekar, D
    PHYTOCHEMISTRY, 1998, 48 (08) : 1453 - 1455
  • [47] Bioactivity of natural O-prenylated phenylpropenes from Illicium anisatum leaves and their derivatives against spider mites and fungal pathogens
    Koeduka, T.
    Sugimoto, K.
    Watanabe, B.
    Someya, N.
    Kawanishi, D.
    Gotoh, T.
    Ozawa, R.
    Takabayashi, J.
    Matsui, K.
    Hiratake, J.
    PLANT BIOLOGY, 2014, 16 (02) : 451 - 456
  • [48] Tabebuialdehydes A-C, cyclopentene dialdehyde derivatives from the roots of Tabebuia rosea
    Sichaem, Jirapast
    Kaennakam, Sutin
    Siripong, Pongpun
    Tip-pyang, Santi
    FITOTERAPIA, 2012, 83 (08) : 1456 - 1459
  • [49] Foetithiophenes C-F, thiophene derivatives from the roots of Ferula foetida
    Chitsazian-Yazdi, Mahsa
    Agnolet, Sara
    Lorenz, Sybille
    Schneider, Bernd
    Es'haghi, Zarrin
    Kasaian, Jamal
    Khameneh, Bahman
    Iranshahi, Mehrdad
    PHARMACEUTICAL BIOLOGY, 2015, 53 (05) : 710 - 714
  • [50] 日本从莽草中分离得到2种新的异戊烯化C6-C3化合物
    高越
    国际中医中药杂志, 2011, (08) : 712 - 712