Bleaching Activity of 4-Phenyl-3-(substituted benzylthio)-4H-1,2,4-triazoles

2002 ◽  
Vol 66 (8) ◽  
pp. 1671-1676 ◽  
Author(s):  
Naotaka YAMADA ◽  
Daisuke KUSANO ◽  
Eiich KUWANO
Keyword(s):  





1995 ◽  
Vol 20 (3) ◽  
pp. 291-297 ◽  
Author(s):  
Koji TAKEHARA ◽  
Naotaka YAMADA ◽  
Hidetoshi HAKIRA ◽  
Eiichi KUWANO ◽  
Eiji TANIGUCHI
Keyword(s):  


1982 ◽  
Vol 37 (11-12) ◽  
pp. 1092-1094 ◽  
Author(s):  
Gerhard Sandmann ◽  
Peter Böger

Abstract New 2-phenylpyridazinones, analogs of 4-chloro-5-methylamino-2-phenylpyridazin-3(2H)ones, were assayed for their phytotoxic activity to interfere with plant pigment formation. Six derivatives with - SCF3, - OCF2CHFCF3, - OCHF2, - CN, or - Br in meta position of the phenyl ring exhibited similar or better bleaching activity than the m-CF3 analog (norflurazon). The activity is predominantly determined by positive σ values and by lipophilicity of the substituent. On the basis of 11 analogs, a quantitative structure-activity relationship by a Hansch equation was accomplished with σm and the lipophilicity parameter π as variables.



10.5109/24434 ◽  
2001 ◽  
Vol 46 (1) ◽  
pp. 219-228
Author(s):  
Naotaka Yamada ◽  
Eiichi Kuwano
Keyword(s):  


1981 ◽  
Vol 15 (3) ◽  
pp. 288-293 ◽  
Author(s):  
G. Sandmann ◽  
K.-J. Kunert ◽  
P. Böger


1968 ◽  
Vol 19 (12) ◽  
pp. 713-717 ◽  
Author(s):  
J. A. Blain ◽  
J. D. E. Patterson ◽  
M. Pearce
Keyword(s):  


10.5109/24461 ◽  
2002 ◽  
Vol 47 (1) ◽  
pp. 67-76
Author(s):  
Naotaka Yamada ◽  
Daisuke Kusano ◽  
Eiichi Kuwano
Keyword(s):  


Weed Science ◽  
1983 ◽  
Vol 31 (3) ◽  
pp. 338-341 ◽  
Author(s):  
Gerhard Sandmann ◽  
Peter Böger

The bleaching effects of norflurazon [4-chloro-5-(methylamino)-2-(α,α,α-trifluoro-m-tolyl)-3 (2H)-pyridazinone] and of oxyfluorfen [2-chloro-1-(3-ethoxy-4-nitrophenoxy)-4-(trifluoromethyl) benzene] were compared using the intact microalgaScenedesmus acutusand the fungusPhycomyces blakesleeanus.Under the influence of oxyfluorfen, but not of norflurazon, pigments and membranes were degraded. This activity is typical for oxyfluorfen. Norflurazon prevented carotene synthesis, but did not cause degradation of carotenoids, chlorophylls, or35S-sulfolipid, a marker of photosynthetic membranes. Furthermore, light-induced ethane evolution byScenedesmusis substantial with oxyfluorfen, but not with norflurazon present. Oxyfluorfen apparently causes radical-initiated peroxidation of polyunsaturated fatty acids.



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