نتایج جستجو برای: furanocoumarin

تعداد نتایج: 128  

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2003
Weimin Li Mary A Schuler May R Berenbaum

Diversification of cytochrome P450 monooxygenases (P450s) is thought to result from antagonistic interactions between plants and their herbivorous enemies. However, little direct evidence demonstrates the relationship between selection by plant toxins and adaptive changes in herbivore P450s. Here we show that the furanocoumarin-metabolic activity of CYP6B proteins in two species of swallowtail ...

Journal: :Biological and Pharmaceutical Bulletin 2004

Journal: :European Journal of Biochemistry 2004

Journal: :Phytochemistry 2012
Yukino Yakabe Masahiro Terato Ataru Higa Koji Yamada Yoshie Kitamura

Our previous study indicated that formation of furanocoumarin phytoalexins could be induced in Glehnia littoralis root cultures by treatment with 10-40 mM ascorbic acid (AsA). This furanocoumarin production is much less evident when G. littoralis roots are treated with AsA under iron-deficient conditions. Instead, two large unknown peaks appeared in the HPLC chromatogram, whose chemical structu...

2009
Sumit Gupta Padmaa M Paarakh Usha Gavani

Fractionation of petroleum ether partitioned ethanol extract and crude petroleum ether extract of the leaves of Murraya koenigii Linn (Rutaceae) led to the isolation of 5,8-dimethyl furanocoumarin (1) and 1-al, 3[6’, 6’ dimethyl 5-hexene] carbazole (2) and β-sitosterol (3). Their structures were elucidated by spectroscopic methods such as UV, IR, NMR and LCMS. All the compounds were isolated fo...

Journal: :The American journal of clinical nutrition 2006
Mary F Paine Wilbur W Widmer Heather L Hart Susan N Pusek Kimberly L Beavers Anne B Criss Sherri S Brown Brian F Thomas Paul B Watkins

BACKGROUND Grapefruit juice (GFJ) enhances the systemic exposure of numerous CYP3A4 drug substrates, including felodipine, by inhibiting intestinal (but not hepatic) first-pass metabolism. Furanocoumarins have been identified as major CYP3A4 inhibitors contained in the juice, but their contribution to the GFJ effect in vivo remains unclear. OBJECTIVE To ascertain whether furanocoumarins media...

Journal: :Protein engineering 2003
Jerome Baudry Weimin Li Liping Pan May R Berenbaum Mary A Schuler

Furanocoumarins represent plant toxins that are used in the treatment of a variety of skin diseases and are metabolized by cytochrome p450 monooxygenases (p450s) existing in insects such as Papilio polyxenes (the black swallowtail). To elucidate the active site in the CYP6B1 protein that is the principal p450 existing in this species, we have constructed a homology model of it based on sequence...

2007
M. Bartnik K. Głowniak

A rapid and sensitive reversed-phase high-performance liquid chromatographic (RP-HPLC) method has been used for determination of furanocoumarins in methanolic extracts of Peucedanum tauricum Bieb. HPLC separation was performed on a C18 analytical column (250 mm × 4 mm i.d., 5-μm particles) with a methanol–water gradient as mobile phase. A second chromatographic system with an acetonitrile–water...

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