Biologically active tetralones from New Caledonian Zygogynum spp.

[1]  F. Roussi,et al.  Isolation and characterization of two new drimanes from Zygogynum baillonii and synthesis of analogues , 2008 .

[2]  T. Efferth,et al.  Cytotoxic and New Tetralone Derivatives from Berchemia floribunda (Wall.) Brongn. , 2006, Chemistry & biodiversity.

[3]  D. Ferreira,et al.  Circular dichroism, a powerful tool for the assessment of absolute configuration of flavonoids. , 2005, Phytochemistry.

[4]  O. Nosjean,et al.  New biologically active linear triterpenes from the bark of three new-caledonian Cupaniopsis species , 2005 .

[5]  I. Abe,et al.  The first plant type III polyketide synthase that catalyzes formation of aromatic heptaketide , 2004, FEBS letters.

[6]  G. Ferry,et al.  Binding of prostaglandins to human PPARgamma: tool assessment and new natural ligands. , 2001, European journal of pharmacology.

[7]  J. Holder,et al.  PPAR-γ agonists: therapeutic role in diabetes, inflammation and cancer , 2000 .

[8]  A. Doust.  Comparative floral ontogeny in Winteraceae. , 2000 .

[9]  K. S. Lee,et al.  Cytotoxic compounds from the roots of Juglans mandshurica. , 1998, Journal of natural products.

[10]  C. Tempěte,et al.  In vitro cytostatic activity of 9-demethoxyporothramycin B , 1995 .

[11]  A. House,et al.  Leaf Essential Oils of the Australian Members of the Genus Zygogynum , 1994 .

[12]  J. Guilhem,et al.  Bubbialine et Bubbialidine, Alcaloïdes Nouveaux Extraits de Zygogynum pauciflorum , 1990 .

[13]  Y. Cheng,et al.  Relationship between the inhibition constant (K1) and the concentration of inhibitor which causes 50 per cent inhibition (I50) of an enzymatic reaction. , 1973, Biochemical pharmacology.

[14]  G. Snatzke,et al.  Chiroptical properties of 4-substituted flavans , 1973 .

[15]  William Gaffield.  Circular dichroism, optical rotatory dispersion and absolute configuration of flavanones, 3-hydroxyflavanones and their glycosides : Determination of aglycone chirality in flavanone glycosides☆ , 1970 .