68939-22-0Relevant articles and documents
Synthesis and aminomethylation of 7-hydroxy-5-methoxyisoflavones
Mrug,Bondarenko,Khilya,Frasinyuk
, p. 235 - 241 (2013/07/26)
A synthetic method for 7-hydroxy-5-methoxyisoflavones starting from 5,7-dihydroxyisoflavones was developed. Dimethylcarbamoylchloride was proposed for protection of the 7-hydroxy group. Aminomethylation of the synthesized 7-hydroxy-5-methoxyisoflavones by formaldehyde aminals was studied.
Studies on Zoospore-Attracting Activity. I. Synthesis of Isoflavones and Their Attracting Activity to Aphanomyces euteiches Zoospore
Sekizaki, Haruo,Yokosawa, Ryozo
, p. 4876 - 4880 (2007/10/02)
Prunetin (2) and its derivatives were synthesized in order to study the relationship between structure and attracting activity to Aphanomyces euteiches zoospore.All of the derivatives (1, 2, 4 and 6), which had a hydroxyl group at the C-5 position in the isoflavone, showed attracting activity, but the methyl ether derivatives (3, 5, 7 and 8) do not have or have very weak attracting activity.The isoflavones (1, 2, and 4) with strong attracting activity also had estrogenic activity.Keywords - isoflavone; prunetin; genistein; biochanin A; 5-methylgenistein; 5-hydroxy-4',7-dimethoxyisoflavone; Aphanomyces euteiches; zoospore; attracting activity; estrogenic activity