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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| Published in: | Chemosphere (Oxford) 1984, Vol.13 (4), p.575-584 |
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| Main Authors: | , , , , |
| Format: | Article |
| Language: | English |
| Subjects: | |
| Citations: | Items that this one cites Items that cite this one |
| Online Access: | Get full text |
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