Predicting toxicity using computed molecular topologies: The example of triorganotin compounds

The LC50 values of eight triorganotin compounds for crab zoeae, Rhithropanopeus harrisii correlate with substituent constants reflecting partitioning effects. Computed molar surface areas predict toxicity as well as any parameter used suggesting that partitioning into lipids controls the toxicity.

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Bibliographic Details
Published in:Chemosphere (Oxford) 1984, Vol.13 (4), p.575-584
Main Authors: Laughlin, Roy B., French, Willie, Johannesen, Rolf B., Guard, H.E., Brinckman, F.E.
Format: Article
Language:English
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