Abstract
The effects on activity against Schistosoma mansoni of further modifications of the diaminodiphenoxyalkanes are reported. Replacement of the amino-group by any of a large number of other groups destroys activity. Activity is retained in the presence of certain substituted (hydroxyalkyl, carboxyalkyl) amino-groups and in some of their aldehyde-bisulphite derivatives. Many variations of the central chain lead to compounds of reduced activity, the outstanding exceptions being a number of but-2-ene derivatives, which retain full activity.
Full text
PDF






Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- CALDWELL A. G., STANDEN O. D. The activity of p-aminophenoxyalkane derivatives against Schistosoma mansoni. Br J Pharmacol Chemother. 1956 Dec;11(4):367–374. doi: 10.1111/j.1476-5381.1956.tb00004.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- RAISON C. G., STANDEN O. D. The schistosomicidal activity of symmetrical diaminodiphenoxyalkanes. Br J Pharmacol Chemother. 1955 Jun;10(2):191–199. doi: 10.1111/j.1476-5381.1955.tb00082.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- STANDEN O. D., WALLS L. P. Effect of ring-substituents on the activity of diphenoxyalkanes against Schistosoma mansoni. Br J Pharmacol Chemother. 1956 Dec;11(4):375–378. doi: 10.1111/j.1476-5381.1956.tb00005.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
