Relationship Between the Shape of Suspension Particle and Ground State Structure of Electrorheological Solid

Feng, Wei; Pei, He; Chen, Zuyao; Wanquan, Jiang

doi:10.1088/0256-307x/17/5/025

Cited by 1 publication

(1 citation statement)

References 1 publication

Supporting

Mentioning

Contrasting

Order By: Relevance

“…[60] 7-(7-hydroxy-3,7-dimethylocta-2,5-dienyloxy)-coumarin (79) HO Clausena excavata, [137] Esenbeckia grandiflora, [138] Phebalium spp., [60] Phellodendron chinense, [147] Zanthoxylum schinifolium [141] Epoxyauraptene (80) O Aegle marmelos, [148] Aster yunnanensis, [149] Citrus spp., [150][151][152] Zanthoxylum schinifolium [140] 7-(3,7-dimethyl-6-oxooct-2-enyloxy)-coumarin (81) O Baccharis darwinii, 153] Citrus hassaku [154] Auraptenal (82) O Capnophyllum peregrinum, [155] Citrus hassaku [154] 7-(5,6-dihydroxy-3,7-dimethylocta-2,7-dienyloxy)-coumarin (83) OH OH Zanthoxylum schinifolium [141] Excavatin A (84) HO OH Clausena excavata [137] Marmin (85) OH HO Aegle marmelos, [156] Aster praealtus. [157] Aurantii fructus immaturus, [158] Citrus grandis, [159] Citrus hassaku, [154] Eremocitrus glauca, [160] Ferula malacophyla , [161] Geijera parviflora, [162] Pituranthos triradiatus, [163] Xue-Fu-Zhu-YuTang [164] Marmin 7-(methylether) (86)…”

Section: R Main Sourcesmentioning

confidence: 99%

Chemistry and Biological Activity of Natural and Synthetic Prenyloxycoumarins †

Curini¹,

Cravotto²,

Epifano³

et al. 2006

CMC

272

170

View full text Add to dashboard Cite

Prenyloxycoumarins and prenyloxyfuranocoumarins (isopentenyloxy-, geranyloxy-, linear and cyclic sesquiterpenyloxy compounds and their biosynthetic derivatives) represent a family of secondary metabolites that have been considered for years just as intermediates of other coumarin-based compounds. Only in the last two decades these secondary metabolites have been recognized as interesting and valuable biologically active natural products. Up to now more than 160 compounds have been isolated from plants mainly belonging to the families of Rutaceae and Umbelliferae, comprising common edible vegetables and fruits like lemons, oranges and grapefruits. In view of the biological activity of some natural prenyloxycoumarins, very recently syntheses of structurally related analogs aimed to establish detailed structure-activity relationships have also been carried out. Many of the isolated prenyloxy- and prenyloxy-furanocoumarins and their semisynthetic derivatives were shown to exert in vitro and in vivo remarkable anti-tumoral, anti-inflammatory and anti-viral effects. The object of this review is to examine in detail the different types of prenyloxycoumarins and prenyloxyfuranocoumarins from the chemical, phytochemical and biological point of view.

show abstract