Structure-activity relationships in photosystem II inhibition by 5-acyl-3-(1-aminoalkylidene)-4-hydroxy-2H-pyran-2,6(3H)-dione derivatives

ISSN:
0048-3575
Source:
Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
Topics:
Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
Type of Medium:
Electronic Resource
URL:
_version_ 1798291509224669184
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