Rauh J J, Holyoke C W, Kleier D A, Presnail J K, Benner E A, Cordova D, Howard M H, Hosie A M, Buckingham S D, Baylis H A, Sattelle D B
DuPont Agricultural Products, Newark, DE 19714-0030, USA.
Invert Neurosci. 1997 Sep-Dec;3(2-3):261-8. doi: 10.1007/BF02480383.
The polycyclic dinitriles are a potent class of insecticides which are non-competitive GABA (gamma-aminobutyric acid) antagonists acting at the convulsant site. Comparison with other classes of GABA convulsant site ligands using molecular modelling has shown significant structural similarities. We have developed a pharmacophore model which unifies this class and some previous classes of GABA convulsants. Key pharmacophore elements are a polarizable functionality separated by a fixed distance from two H-bond accepting elements. This model is based on information from X-ray crystal structures and Sybyl using the Tripos force field. Using this pharmacophore model, numerous structural modifications were explored to enhance understanding of structure-activity relationships at the GABA receptor convulsant site of insects and mammals. A radiolabelled bicyclic dinitrile, [3H]BIDN [3H]3,3-bis-trifluoromethyl-bicyclo[2,2,1]heptane-2,2-dicarbonitrile+ ++), was prepared from this area of chemistry and was used as a probe for the interaction of polycyclic dinitriles at the target site.
多环二腈是一类强效杀虫剂,它们是作用于惊厥位点的非竞争性γ-氨基丁酸(GABA)拮抗剂。通过分子建模与其他类GABA惊厥位点配体进行比较,结果显示出显著的结构相似性。我们已经开发出一种药效团模型,该模型统一了这一类以及之前的一些类GABA惊厥剂。关键的药效团元素是一个可极化官能团,它与两个氢键接受元素相隔固定距离。该模型基于来自X射线晶体结构的信息以及使用Tripos力场的Sybyl软件。利用这个药效团模型,人们探索了众多结构修饰,以增进对昆虫和哺乳动物GABA受体惊厥位点结构-活性关系的理解。一种放射性标记的双环二腈,即[³H]BIDN([³H]3,3-双三氟甲基-双环[2,2,1]庚烷-2,2-二腈),是从这一化学领域制备出来的,并被用作多环二腈在靶位点相互作用的探针。