Inhibitors of Phenylalanine Ammonia-Lyase: 2-Aminoindan-2-phosphonic Acid and Related Compounds

1992 ◽  
Vol 1992 (6) ◽  
pp. 625-628 ◽  
Author(s):  
Jerzy Zoń ◽  
Nikolaus Amrhein
1968 ◽  
Vol 23 (11) ◽  
pp. 1517-1521 ◽  
Author(s):  
S. M. A. D. Zayed ◽  
A. Hassan ◽  
I. M. I. Fakhr

In search for effective organophosphorus esters against the larva of the cotton leaf worm (Prodenia litura F), some α-hydroxy phosphonic acid dimethyl esters and related compounds have been synthesized. The effect of substitution on the antiesterase activity and toxicity towards Prodenia larvae has been investigated.The infra-red spectra of the prepared phosphorus esters are discussed.


2006 ◽  
Vol 61 (7-8) ◽  
pp. 578-582 ◽  
Author(s):  
Atsumi Shimada ◽  
Yasuo Kimura

Glyphosate showed a remarkable effect inducing the change of flower symmetry from the actinomorphic to the zygomorphic type in Petunia hybrida. Glyphosate [N-(phosphonomethyl) glycine] reduced the anthocyanin content and showed a weak inhibitory effect against phenylalanine ammonia-lyase (PAL) activity. ʟ-2-Aminooxy-3-phenylpropionic acid (APA), an inhibitor of PAL activity, reduced the anthocyanin content but had no effect on flower shape. Additional phenylalanine or trans-cinnamic acid, the intermediates of glyphosate inhibition against PAL activity, could not recover the change of flower shape induced by glyphosate. These results suggested that the reduction of PAL activity alone could not account for the two characteristic changes of flower symmetry and pigmentation induced by glyphosate. On the other hand, the results of application of glyphosate-related compounds suggested that the structure of glyphosate contributed to induce the morphological change of Petunia flower. Glyphosate may thus be a very useful agent in the elucidation of unresolved questions of flower morphogenesis and the related metabolism.


1974 ◽  
Vol 17 (6) ◽  
pp. 642-645 ◽  
Author(s):  
Mercedes Fuertes ◽  
Joseph T. Witkowski ◽  
David G. Streeter ◽  
Roland K. Robins

1969 ◽  
Vol 24 (11) ◽  
pp. 1381-1384 ◽  
Author(s):  
G. Lassmann ◽  
W. Damerau ◽  
Kh. Lohs

The formation and conversion of primary radicals in the irradiated phosphonic acid ester trichlorphon and some related compounds at 77 °K have been studied by ESR. The irreversible changes of spectra by annealing of the sample demonstrate that the chlorine-containing radical type R-CCl21 formed at room temperature represents a secondary type having a precursor with a short half life in the form of a primary radical of similar structure but different conformation which is stable from 77°K to 245°K. A further radical formed at 77°K in trichlorphon is This type disappears at -60°C. In related compounds (DDVP and the acetic acid ester of trichlorphon) a similar radical CH2OR is induced, which in contrast to trichlorphon is converted into an oxygen radical with g=2,0076 and g= 2,017.


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