Structure-activity relationships in photosystem II inhibition by 5-acyl-3-(1-aminoalkylidene)-4-hydroxy-2H-pyran-2,6(3H)-dione derivatives
Yoneyama, K. ; Nakajima, Y. ; Konnai, M. ; Iwamura, H. ; Asami, T. ; Takahashi, N. ; Yoshida, S.
Amsterdam : Elsevier
Amsterdam : Elsevier
ISSN: |
0048-3575
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Source: |
Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
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Topics: |
Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
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Type of Medium: |
Electronic Resource
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URL: |
_version_ | 1798291509224669184 |
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autor | Yoneyama, K. Nakajima, Y. Konnai, M. Iwamura, H. Asami, T. Takahashi, N. Yoshida, S. |
autorsonst | Yoneyama, K. Nakajima, Y. Konnai, M. Iwamura, H. Asami, T. Takahashi, N. Yoshida, S. |
book_url | http://dx.doi.org/10.1016/0048-3575(91)90083-X |
datenlieferant | nat_lic_papers |
fussnote | Quantitative structure-activity relationships in photosystem II (PS II) inhibition by 5-acyl-3-(1-aminoalkylidene)-4-hydroxy-2H-pyran-2,6(3H)-dione derivatives were analyzed. The results demonstrate that overall lipophilicity of the molecule is a major determinant for the activity as in the case for typical PS II inhibitors including phenylurea herbicides. In addition, the activity of the substituted N-benzyl derivatives was found to depend not only on the lipophilicity but also on both the electronic and steric characters of the substituents. |
hauptsatz | hsatz_simple |
identnr | NLZ184420180 |
issn | 0048-3575 |
journal_name | Pesticide Biochemistry and Physiology |
materialart | 1 |
package_name | Elsevier |
publikationsort | Amsterdam |
publisher | Elsevier |
reference | 41 (1991), S. 288-295 |
search_space | articles |
shingle_author_1 | Yoneyama, K. Nakajima, Y. Konnai, M. Iwamura, H. Asami, T. Takahashi, N. Yoshida, S. |
shingle_author_2 | Yoneyama, K. Nakajima, Y. Konnai, M. Iwamura, H. Asami, T. Takahashi, N. Yoshida, S. |
shingle_author_3 | Yoneyama, K. Nakajima, Y. Konnai, M. Iwamura, H. Asami, T. Takahashi, N. Yoshida, S. |
shingle_author_4 | Yoneyama, K. Nakajima, Y. Konnai, M. Iwamura, H. Asami, T. Takahashi, N. Yoshida, S. |
shingle_catch_all_1 | Yoneyama, K. Nakajima, Y. Konnai, M. Iwamura, H. Asami, T. Takahashi, N. Yoshida, S. Structure-activity relationships in photosystem II inhibition by 5-acyl-3-(1-aminoalkylidene)-4-hydroxy-2H-pyran-2,6(3H)-dione derivatives 0048-3575 00483575 Elsevier |
shingle_catch_all_2 | Yoneyama, K. Nakajima, Y. Konnai, M. Iwamura, H. Asami, T. Takahashi, N. Yoshida, S. Structure-activity relationships in photosystem II inhibition by 5-acyl-3-(1-aminoalkylidene)-4-hydroxy-2H-pyran-2,6(3H)-dione derivatives 0048-3575 00483575 Elsevier |
shingle_catch_all_3 | Yoneyama, K. Nakajima, Y. Konnai, M. Iwamura, H. Asami, T. Takahashi, N. Yoshida, S. Structure-activity relationships in photosystem II inhibition by 5-acyl-3-(1-aminoalkylidene)-4-hydroxy-2H-pyran-2,6(3H)-dione derivatives 0048-3575 00483575 Elsevier |
shingle_catch_all_4 | Yoneyama, K. Nakajima, Y. Konnai, M. Iwamura, H. Asami, T. Takahashi, N. Yoshida, S. Structure-activity relationships in photosystem II inhibition by 5-acyl-3-(1-aminoalkylidene)-4-hydroxy-2H-pyran-2,6(3H)-dione derivatives 0048-3575 00483575 Elsevier |
shingle_title_1 | Structure-activity relationships in photosystem II inhibition by 5-acyl-3-(1-aminoalkylidene)-4-hydroxy-2H-pyran-2,6(3H)-dione derivatives |
shingle_title_2 | Structure-activity relationships in photosystem II inhibition by 5-acyl-3-(1-aminoalkylidene)-4-hydroxy-2H-pyran-2,6(3H)-dione derivatives |
shingle_title_3 | Structure-activity relationships in photosystem II inhibition by 5-acyl-3-(1-aminoalkylidene)-4-hydroxy-2H-pyran-2,6(3H)-dione derivatives |
shingle_title_4 | Structure-activity relationships in photosystem II inhibition by 5-acyl-3-(1-aminoalkylidene)-4-hydroxy-2H-pyran-2,6(3H)-dione derivatives |
sigel_instance_filter | dkfz geomar wilbert ipn albert fhp |
source_archive | Elsevier Journal Backfiles on ScienceDirect 1907 - 2002 |
timestamp | 2024-05-06T08:33:45.184Z |
titel | Structure-activity relationships in photosystem II inhibition by 5-acyl-3-(1-aminoalkylidene)-4-hydroxy-2H-pyran-2,6(3H)-dione derivatives |
titel_suche | Structure-activity relationships in photosystem II inhibition by 5-acyl-3-(1-aminoalkylidene)-4-hydroxy-2H-pyran-2,6(3H)-dione derivatives Quantitative structure-activity relationships in photosystem II (PS II) inhibition by 5-acyl-3-(1-aminoalkylidene)-4-hydroxy-2H-pyran-2,6(3H)-dione derivatives were analyzed. The results demonstrate that overall lipophilicity of the molecule is a major determinant for the activity as in the case for typical PS II inhibitors including phenylurea herbicides. In addition, the activity of the substituted N-benzyl derivatives was found to depend not only on the lipophilicity but also on both the electronic and steric characters of the substituents. |
topic | ZA-ZE |
uid | nat_lic_papers_NLZ184420180 |