Neonicotinoid Insecticides: Highlights of a Symposium on Strategic Molecular Designs

被引:56
|
作者
Tomizawa, Motohiro [1 ]
Casida, John E. [2 ]
机构
[1] Gifu Univ, Fac Educ, Gifu 5011193, Japan
[2] Univ Calif Berkeley, Dept Environm Sci Policy & Management, Environm Chem & Toxicol Lab, Berkeley, CA 94720 USA
关键词
imidacloprid; insecticide design; neonicotinoids; nicotinic acetylcholine receptor;
D O I
10.1021/jf103856c
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
Neonicotinoids are the newest of the five major classes of insecticides (the others are chlorinated hydrocarbons, organophosphorus compounds, methylcarbamates, and pyrethroids), and they make up approximately one-fourth of the world insecticide market. Nithiazine was the lead compound from Shell Development Co. in California later optimized by Shinzo Kagabu of Nihon Tokushu Noyaku Seizo to increase the potency and photostability, resulting in imidacloprid and thiacloprid. These discoveries are the basis for the International Award for Research in Agrochemicals of the American Chemical Society presented in 2010 to Professor Shinzo Kagabu. Five other neonicotinoids were added by others for the current set of seven commercial compounds. This symposium considers the progress in discovery and development of novel chemotype nicotinic insecticides with enhanced effectiveness, unique biological properties, and maximal safety. Chemorational approaches considered include physicochemical properties, metabolic activation and detoxification, and chemical and structural biology aspects potentially facilitating receptor structure-guided insecticide design.
引用
收藏
页码:2883 / 2886
页数:4
相关论文
共 50 条
  • [1] Molecular Mechanism of Action of Neonicotinoid Insecticides
    Thany, Steeve H.
    INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2023, 24 (06)
  • [2] Neonicotinoid Insecticides: Molecular Targets, Resistance, and Toxicity
    Matsuda, Kazuhiko
    Ihara, Makoto
    Sattelle, David B.
    ANNUAL REVIEW OF PHARMACOLOGY AND TOXICOLOGY, VOL 60, 2020, 60 : 241 - 255
  • [3] Unravelling the Molecular Determinants of Bee Sensitivity to Neonicotinoid Insecticides
    Manjon, Cristina
    Troczka, Bartlomiej J.
    Zaworra, Marion
    Beadle, Katherine
    Randall, Emma
    Hertlein, Gillian
    Singh, Kumar Saurabh
    Zimmer, Christoph T.
    Homem, Rafael A.
    Lueke, Bettina
    Reid, Rebecca
    Kor, Laura
    Kohler, Maxie
    Benting, Juergen
    Williamson, Martin S.
    Davies, T. G. Emyr
    Field, Linda M.
    Bass, Chris
    Nauen, Ralf
    CURRENT BIOLOGY, 2018, 28 (07) : 1137 - +
  • [4] Molecular Recognition of Neonicotinoid Insecticides: The Determinants of Life or Death
    Tomizawa, Motohiro
    Casida, John E.
    ACCOUNTS OF CHEMICAL RESEARCH, 2009, 42 (02) : 260 - 269
  • [5] In Focus: Neonicotinoid insecticides
    Nauen, Ralf
    Jeschke, Peter
    Copping, Len
    PEST MANAGEMENT SCIENCE, 2008, 64 (11) : 1081 - 1081
  • [6] Pharmacophore of neonicotinoid insecticides
    Kagabu, Shinzo
    JOURNAL OF PESTICIDE SCIENCE, 2008, 33 (01) : 9 - 13
  • [7] Molecular similarity and structure-activity relationship of neonicotinoid insecticides
    Nakayama, A
    JOURNAL OF PESTICIDE SCIENCE, 1998, 23 (03): : 336 - 343
  • [8] Molecular Recognition of Neonicotinoid Insecticides by Honeybee Nicotinic Receptors and ACHBP Homologues
    Ulens, Chris
    Bisseling, Quinty
    Brams, Marijke
    Mehregan, Aujan
    Evans, Genevieve L.
    Pasini, Diletta
    Beard, Hester
    Verhelst, Steven
    Fish, Alexander
    van Dorst, Sofie
    Kambara, Kumiko
    Bertrand, Daniel
    BIOPHYSICAL JOURNAL, 2020, 118 (03) : 585A - 585A
  • [9] Molecular similarity analysis and 3D-QSAR of neonicotinoid insecticides
    Sukekawa, M
    Nakayama, A
    MOLECULAR MODELING AND PREDICTION OF BIOACTIVITY, 2000, : 340 - 341
  • [10] Pharmacophore model for neonicotinoid insecticides
    Li, Jian
    Ju, Xiu Lian
    Jiang, Feng Chao
    CHINESE CHEMICAL LETTERS, 2008, 19 (05) : 619 - 622