Inhibitory Activities of 3-Thiophenecarboxylic Acid and Related Compounds on Plant Growth

1994 ◽  
Vol 58 (7) ◽  
pp. 1336-1337
Author(s):  
Yoshihiko Inamori ◽  
Chikaaki Muro ◽  
Kyoko Osaka ◽  
Yuichiro Funakoshi ◽  
Yoshihide Usami ◽  
...  
Keyword(s):  
Plant Growth ◽  
Inhibitory Activities ◽  
Related Compounds

scholarly journals Synthesis of Stereoisomers of Ipconazole and Their Fungicidal and Plant Growth Inhibitory Activities

1997 ◽  
Vol 22 (2) ◽  
pp. 119-125 ◽  
Author(s):  
Atsushi ITO ◽  
Toshihide SAISHOJI ◽  
Satoru KUMAZAWA
Keyword(s):  
Plant Growth ◽  
Growth Inhibitory ◽  
Inhibitory Activities

Stereoselective Syntheses of All Stereoisomers of Lariciresinol and Their Plant Growth Inhibitory Activities

2011 ◽  
Vol 59 (24) ◽  
pp. 13089-13095 ◽  
Author(s):  
Hisashi Nishiwaki ◽  
Mitsuko Kumamoto ◽  
Yoshihiro Shuto ◽  
Satoshi Yamauchi
Keyword(s):  
Plant Growth ◽  
Growth Inhibitory ◽  
Inhibitory Activities ◽  
Stereoselective Syntheses

scholarly journals Phytogrowth-Inhibitory Activities of .BETA.-Dolabrin and .GAMMA.-Thujaplicin, Hinokitiol-Related Compounds and Constituents of Thujopsis dolabrata Sieb. et Zucc. var hondai MAKINO.

2000 ◽  
Vol 23 (5) ◽  
pp. 645-648 ◽  
Author(s):  
Yoshikazu SAKAGAMI ◽  
Yoshihiko INAMORI ◽  
Nami ISOYAMA ◽  
Hiroshi TSUJIBO ◽  
Toshihiro OKABE ◽  
...  
Keyword(s):  
Inhibitory Activities ◽  
Related Compounds

scholarly journals Inhibitory activities and inhibition specificities of caffeic acid derivatives and related compounds toward 5-lipoxygenase.

1989 ◽  
Vol 37 (4) ◽  
pp. 1039-1043 ◽  
Author(s):  
Masanori SUGIURA ◽  
Youichiro NAITO ◽  
Yasunari YAMAURA ◽  
Chikara FUKAYA ◽  
Kazumasa YOKOYAMA
Keyword(s):  
Caffeic Acid ◽  
Caffeic Acid Derivatives ◽  
Inhibitory Activities ◽  
Related Compounds

Levels of ACC and related compounds in exudate and extracts of canola seeds treated with ACC deaminase-containing plant growth-promoting bacteria

2001 ◽  
Vol 47 (4) ◽  
pp. 368-372 ◽  
Author(s):  
Donna M Penrose ◽  
Bernard R Glick
Keyword(s):  
Plant Growth ◽  
Acc Deaminase ◽  
Aminobutyric Acid ◽  
Plant Growth Promoting Bacteria ◽  
Canola Seed ◽  
Test Part ◽  
Seed Exudate ◽  
Plant Growth Promoting ◽  
Growth Promoting ◽  
Related Compounds

It was previously proposed that plant growth-promoting bacteria that possess 1-aminocyclopropane-1-carboxylic acid (ACC) deaminase could utilize ACC that is present in the exudate of germinating canola seeds. The uptake and cleavage of ACC by these bacteria would lower the level of ACC, and thus ethylene within the plant, and reduce the extent of its inhibition on root elongation. To test part of the above mentioned model, ACC levels were monitored in canola seed tissues and exudate during germination. Lower amounts of ACC were present in the exudate and tissues of seeds treated with the plant growth-promoting bacterium Enterobacter cloacae CAL3, than in control seeds treated with MgSO4. The ACC-related compounds, α- and γ-aminobutyric acids, both known to stimulate ethylene production, were also measured in the canola seed exudate and tissues. Approximately the same levels of α-aminobutyric acid were present in the exudates of the bacterium-treated seeds and the control seeds, but the amount of α-aminobutyric acid was lower in the tissues of the bacterium-treated seeds than in the control seeds. Smaller quantities of γ-aminobutyric acid were seen in both the exudate and tissues of the E. cloacae CAL3-treated seeds than in the control seeds.Key words: ACC ethylene, canola, seed extract, seed exudate, plant growth-promoting bacteria.

Growth-inhibitory activities of some 1,4-naphthoquinones and related compounds on Staphylococcus aureus and Escherichia coli

1968 ◽  
Vol 14 (6) ◽  
pp. 661-666 ◽  
Author(s):  
G. J. Leahy ◽  
D. J Currie ◽  
H. L. Holmes ◽  
J. R. Maltman
Keyword(s):  
Escherichia Coli ◽  
Staphylococcus Aureus ◽  
Electron Transport ◽  
Electron Transport Chain ◽  
Growth Inhibitory ◽  
Transport Chain ◽  
Half Wave ◽  
Inhibitory Activities ◽  
Related Compounds

Growth-inhibitory activities of some or all of 98 1,4-naphthoquinones and 16 related compounds on Escherichia coli and two strains of Staphylococcus aureus were determined alone or in combination. These values, when plotted against their polarographic half-wave potentials and those of their C2-n-butylthio analogs support the hypothesis that these compounds, or the products resulting from their reaction with a protein nucleophile, function by short-circuiting one or other of the quinones present in the electron-transport chain.

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