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The binding affinity to intact Sf-9 cells was measured in a series of N-t-butyl-N,N′-dibenzoylhydrazine congeners. The benzene ring close to the t-butyl group of the compounds was substituted with Cl at the ortho-position and the other benzene ring was variously substituted at the para-position. The effects of the substituent on the binding affinity were analyzed quantitatively using the Hansch–Fujita QSAR method. The introduction of hydrophobic and electron-donating substituents at the para-position enhanced the binding affinity toward the ecdysone receptor protein. Steric repulsion between the substituent and receptor surface was also suggested. © Pesticide Science Society of Japan

QSAR for Binding Affinity of Substituted Dibenzoylhydrazines to Intact Sf-9 Cells