Planta Med 2003; 69(1): 15-20
DOI: 10.1055/s-2003-37030
Original Paper
Pharmacology
© Georg Thieme Verlag Stuttgart · New York

Cancer Chemopreventive in vitro Activities of Isoflavones Isolated from Iris germanica

Eckhard Wollenweber1 , Jan Frederik Stevens2 , 4 , Karin Klimo3 , Jutta Knauft3 , Norbert Frank3 , Clarissa Gerhäuser3
  • 1Institut für Botanik, Technische Universität, Darmstadt, Germany
  • 2Department of Chemistry, Oregon State University, Corvallis, OR, USA
  • 3AG Chemoprävention (C0202), Deutsches Krebsforschungszentrum, Heidelberg, Germany
  • 4Present address: Institut für Pflanzenbiochemie, Halle/Saale, Germany
Further Information

Publication History

Received: May 3, 2002

Accepted: August 13, 2002

Publication Date:
04 February 2003 (online)

Abstract

Six known isoflavones were isolated from the rhizomes of Iris germanica, and were established by UV, MS and NMR techniques as irisolidone (1), irisolidone 7-O-α-D-glucoside (1a), irigenin (2), irilone (3), iriflogenin (4), and iriskashmirianin (5). These compounds were examined for their cancer chemopreventive potential. They were shown to be potent inhibitors of cytochrome P450 1A activity with IC50 values in the range 0.25 - 4.9 μM. The isoflavones 2, 3 and 5 displayed moderate activity as inducers of NAD(P)H:quinone reductase (QR) in cultured mouse Hepa 1c1c7 cells, with CD values (concentration required to double the specific activity of QR) of 3.5 - 16.7 μM, whereas weak activity was observed with compounds 4 and 5 in the radical (DPPH) scavenging bioassay (IC50 values 89.6 and 120.3 μM, respectively). With respect to anti-tumor promoting potential based on anti-inflammatory mechanisms, none of the compounds demonstrated significant activity in the concentration range tested.

Abbreviations

APCI:atmospheric pressure chemical ionization

CD:concentration required for doubling of the specific activity of NAD(P)H:quinone reductase

Cox:cyclooxygenase

Cyp:cytochrome P450

DAD:diode-array detector

DPPH:1,1-diphenyl-2-picrylhydrazyl

HMBC:heteronuclear multiple bond correlation

IC50:half-maximal inhibitory concentration

iNOS:inducible nitric oxide synthase

NF:naphthoflavone

QR:NAD(P)H:quinone reductase

SC50:half-maximal scavenging concentration

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Prof. Dr. E. Wollenweber

Institut für Botanik

Technische Universität Darmstadt

Schnittspahnstr. 4

D-64287 Darmstadt

Germany

Email: wollenweber@bio.tu-darmstadt.de

Fax: +49 6151 16 4630

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