Quantitative structure-activity studies of octopaminergic 2-(Arylimino)thiazolidines and Oxazolidines against the nervous system of Periplaneta americana L. |
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Authors: | Akinori Hirashima Jun Tomita Canping Pan Eiji Taniguchi Morifusa Eto |
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Affiliation: | a Department of Agricultural Chemistry, Kyushu University, Fukuoka 812-81, Japan b Miyakonojo National College of Technology, 473-1 Yoshio-cho, Miyakonojo 885, Japan |
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Abstract: | The quantitative structure-activity relationship (QSAR) of octopaminergic 2-(arylimino)thiazolidines (AITs) and 2-(arylimino)oxazolidines (AIOs) against the thoracic nerve cord of the American cockroach, Periplaneta americana L., was analysed using reported physicochemical parameters and regression analysis. The more electron-donating, the less bulky at m-position, and the more hydrophobic the substituent, the greater the activity. The plots of observed log Vmax values against calculated log Vmax values having substituents on the m-position deviated downwards from those of compounds having substituents at the o- and/or p-positions. The more hydrophobic and the more electron-withdrawing the substituent, the greater the activity. AIO with a 2,3,4-trichlorophenyl group (58) was more active than its thiazolidine derivative, 2-(2,3,4-trichlorophenylimino)thiazolidine (38) in terms of Vmax:Vmax of 58 was 30% relative to octopamine (OA), whereas that of 38 has been 9% relative to OA, respectively. Superimposition of energy-minimized OA and 58 revealed structural and conformational similarities that might account for the high activity of 58. |
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