• Chỉ mục bởi
  • Năm xuất bản
LIÊN KẾT WEBSITE

Phenolic constituents from the leaves of Cratoxylum formosum ssp. pruniflorum

Xiong J. Department of Natural Products Chemistry, School of Pharmacy, Fudan University, Shanghai 201203, China|
Hu J.-F. | Yang G.-X. | Fan H. | Zhao Y. | Wang L.-J. Department of Chemistry, Hoa Lu University, Ninh Binh 40000, Viet Nam| Hong Z.-L. Shanghai Engineering Research Center of Molecular Therapeutics and New Drug Development, East China Normal University, Shanghai 200062, China| Bui V.-B. Department of Chemistry, East China Normal University, Shanghai 200062, China| Liu X.-H. Department of Pharmacology, School of Pharmacy, Fudan University, Shanghai 201203, China|

Fitoterapia Số , năm 2014 (Tập 94, trang 114-119)

ISSN: 0367326X

ISSN: 0367326X

DOI: 10.1016/j.fitote.2014.02.002

Tài liệu thuộc danh mục: Scopus

Article

English

Từ khóa: 11 hydroxy 5 methoxy 2,2,9 trimethyl 2h anthra [1,2 b] pyran 7,12 dione; 2' hydroxy 4',4' dimethyl pyran 1,5 dihydroxyxanthone; 2' hydroxymethyl 3',3' dimethyl dihydrofuran 1,5 dihydroxyxanthone; 2,3 trans dihydro kaemferol; 5,7 dihydroxychromone; amyloid beta protein[25-35]; flavanone; formosumone a; formoxanthone c; gb 1; gb 1a; gb 2; gb 2a; lipopolysaccharide; neuroprotective agent; nitric oxide; phenol derivative; phloroglucinol; physcion; toxyloxanthone b; unclassified drug; vismiaquinone; vismione b; vismione d; 11 hydroxy 5 methoxy 2,2,9 trimethyl 2h anthra[1,2 b]pyran 7,12 dione; 2' hydroxy 4',4' dimethylpyran 1,5 dihydroxyxanthone; 2' hydroxymethyl 3',3' dimethyldihydrofuran 1,5 dihydroxyxanthone; 2,3 dihydrokaemferol; amyloid beta protein[25-35]; antiinflammatory agent; Cratoxylum formosum pruniflorum extract; formosumone A; formoxanthone C; n(g) methylarginine; naringenin(3-8) 5,7 dihydroxychromone; nitric oxide; plant extract; pruniflorone M; pruniflorone N; toxyloxanthone B; vismione B; vismione D; anthraquinone derivative; antiinflammatory agent; flavonoid; neuroprotective agent; phenol derivative; plant extract; xanthone derivative; animal cell; animal experiment; antineuroinflammatory activity; article; carbon nuclear magnetic resonance; cell viability; Clusiaceae; comparative study; controlled study; Cratoxylum formosum ssp pruniflorumm; drug activity; drug isolation; drug structure; heteronuclear multiple bond correlation; IC 50; microglia; mouse; neuroblastoma cell; neuroprotection; nonhuman; nuclear Overhauser effect; physical chemistry; plant leaf; priority journal; Southeast Asia; tea; antiinflammatory activity; Article; biosynthesis; cell viability assay; Cratoxylum formosum pruniflorum; drug efficacy; human; human cell; medicinal plant; nervous system inflammation; structure analysis; animal; cell line; cell survival; chemical structure; chemistry; drug effects; isolation and purification; metabolism; nuclear magnetic resonance spectroscopy; plant leaf; Clusiaceae; Cratoxylum formosum; Murinae; Animals; Anthraquinones; Anti-Inflammatory Agents; Cell Line; Cell Survival; Clusiaceae; Flavonoids; Lipopolysaccharides; Magnetic Resonance Spectroscopy; Mice; Molecular Structure; Neuroprotective Agents; Nitric Oxide; Phenols; Plant Extracts; Plant Leaves; Xanthones
Tóm tắt tiếng anh
One (formosumone A, 1) new and fifteen (2-16) known phenolic compounds were isolated from the leaves of Cratoxylum formosum ssp. pruniflorumm, a substitute for the popular bitter nail tea ("Kuding Tea") generally used in Southeast Asia. Their structures were determined by extensive spectroscopic analysis and by comparison with literature data. Compound 1 possesses a rare scaffold of a flavanone coupled with a phloroglucinol moiety, representing the first example of such a scaffold from the Clusiaceae family. Among the isolates, toxyloxanthone B (11) and vismione D (12) were found to show remarkable anti-neuroinflammatory effects by inhibiting nitric oxide (NO) production in lipopolysaccharide (LPS)-stimulated murine BV-2 microglial cells. Additionally, toxyloxanthone B (11) exhibited significant neuroprotective effect against β-amyloid25-35 (Aβ25-35)-induced cell viability decrease in SH-SY5Y neuroblastoma cells. © 2014 Elsevier B.V.

Xem chi tiết