Studies on Neurotransmitter Receptors and Their Ligands(on prominent achievement)(Society Awards 2004)
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概要
- 論文の詳細を見る
Structure-activity relationship studies of y-aminobutyric acid (GABA) antagonists revealed that there are structural differences between the antagonist binding sites of houseflies and rats. The results point to the feasibility of the development of safe insecticides targeting insect GABA receptors. Studies with cockroach nerve cords demonstrated unique actions of dinotefuran and benzylidene anabaseines on insect nicotinic acetylcholine (ACh) receptors. Tyramine (TA) was shown to be a bioactive amine in the silkworm, and the structures of TA receptor ligands were disclosed.
- 日本農薬学会の論文
- 2004-05-20
著者
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Ozoe Yoshihisa
Department of Life Science and Biotechnology, Faculty of Life and Environmental Science, Shimane Uni
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Ozoe Yoshihisa
Department Of Bioresource Science Faculty Of Agriculture Shimane University
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Ozoe Yoshihisa
Department Of Life Science And Biotechnology Faculty Of Life And Environmental Science Shimane Unive
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- Potency of Isomers of 8-Isopropyl-6-oxabicyclo[3.2.1]octan-7-one at the Picrotoxinin Binding Site in the GABA-Gated Chloride Channel in Rat Brain
- Sesquilignan Haedoxans : Interaction with the GABA_A Receptor in Rat Brain
- Six-membered Cyclic Phosphonate GABA Antagonists, 2,5-Disubstituted 1,3,2-Dioxaphosphorinanes
- Octopamine Receptors in the Head of the Larva of the Common Cutworm, Spodoptera litura FABRICIUS (Lepidoptera: Noctuidae): Effects of Agonists and Antagonists
- Resistance of Housefly Bicyclophosphate Binding Sites to Detergent Extraction(Biological Chemistry)
- Studies on Neurotransmitter Receptors and Their Ligands(on prominent achievement)(Society Awards 2004)
- Bombyx mori phenolamine receptors : a comparative molecular biological study
- Affinity of 3-benzylidene- and 3-cinnamylidenemyosmine analogues for Periplaneta americana nicotinic acetylcholine receptors
- A Secreted Placental Alkaline Phosphatase-Based Reporter Assay System for Screening of Compounds Acting at an Octopamine Receptor Stably Expressed in a Mammalian Cell Line