Herbicidal Activity of Caprolactam Derivatives
نویسندگان
چکیده
منابع مشابه
Herbicidal Activity of Mimosine and Its Derivatives
Mimosine [β-[N-(3-hydroxy-4-oxypyridyl)]-α-aminopropionic acid] is a non-protein amino acid, and is a major compound present in all plant parts of Mimosaceae, which includes Leucaena (Leucaena leucocephala), Leucaena glauca, and other legumes belonging to Mimosa spp.. Structurally, mimosine is an analog of dihydroxyphenylalanine with a 3-hydroxy-4-pyridone ring instead of a 3,4-dihydroxy-phenyl...
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interest in agrochemicals and drugs. Aryl group substituted pyrazoles and imidazoles, in particular, have been studied because their biological activities are strongly dependent on their substituents on the pyrazole ring system. 1,5-Diaryl substituted pyrazole (SR141716A, 1), which has a hydrazide group on the 3-position of the pyrazole ring, has recently been synthesized and identified as the ...
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Three new hydrazide and five new hydrazonoyl derivatives were synthesized. The chemical structures of these compounds were confirmed by 1H-NMR, IR spectroscopy and elemental analysis. The prepared compounds were tested for their activity to inhibit photosynthetic electron transport in spinach chloroplasts and growth of the green algae Chlorella vulgaris. IC50 values of these compounds varied in...
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The pyrazine ring is a part of many polycyclic compounds of biological and/or industrial significance; examples are quinoxalines, phenazines, and bio-luminescent natural products pteridines, flavins and their derivatives. All these compounds are characterized by a low lying unoccupied π-molecular orbital and by the ability to act as bridging ligand. Due to these two properties 1,4-diazines, and...
متن کاملAmino-caprolactam derivatives as gamma-secretase inhibitors.
A series of amino-caprolactam sulfonamides were developed from a screening hit. Compounds with good in vitro and in vivo gamma-secretase activity are reported.
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ژورنال
عنوان ژورنال: Journal of the Faculty of Agriculture, Kyushu University
سال: 1976
ISSN: 0023-6152
DOI: 10.5109/22889