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Activity-guided isolation of constituents of Tephrosia purpurea with the potential to induce the phase II enzyme, quinone reductase.

作者信息

Chang L C, Gerhäuser C, Song L, Farnsworth N R, Pezzuto J M, Kinghorn A D

机构信息

Department of Medical Chemistry and Pharmacognosy, College of Pharmacy, University of Illinois at Chicago 60612, USA.

出版信息

J Nat Prod. 1997 Sep;60(9):869-73. doi: 10.1021/np970236p.

DOI:10.1021/np970236p
PMID:9322358
Abstract

An isoflavone, 7,4'-dihydroxy-3',5'-dimethoxyisoflavone (1), and a chalcone, (+)-tephropurpurin (2), both novel compounds, as well as six constituents of known structure, (+)-purpurin (3), pongamol (4), lanceolatin B (5), (-)-maackiain (6), (-)-3-hydroxy-4-methoxy-8,9-methylene-dioxypterocarpan (7), and (-)-medicarpin (8), were obtained as active compounds from Tephrosia purpurea, using a bioassay based on the induction of quinone reductase (QR) activity with cultured Hepa 1c1c7 mouse hepatoma cells. Additionally, three inactive compounds of known structure, 3'-methoxydaidzein, desmoxyphyllin B, and 3,9-dihydroxy-8-methoxycoumestan, were isolated and identified. The structure elucidation of compounds 1 and 2 was carried out by spectral data interpretation.

摘要

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