
Journal of Medicinal Chemistry p. 947 - 952 (1982)
Update date:2022-08-04
Topics:
El-Fehail Ali
Dandridge
Gleason
et al.
A series of N',N''-bis(aryl)- and N',N''-(aralkyl)imidodisulfamides was prepared and evaluated as antagonists of slow-reacting substance of anaphylaxis (SRS-A) induced contractions of isolated guinea pig ileum. Some of these compounds, notably N',N''-bis(4-phenylbutyl)- N',N''-bis[2-(4-chlorophenyl)ethyl]-, and N',N''-bis[2-(4-bromophenyl)ethyl]imidodisulfamides (16, 22, and 26), were moderately potent and selective antagonists of SRS-A. The influence of lipophilic (π) and electronic (σ) factors on SRS-A antagonist activity appears to be of considerable importance to the derivation of potent and selective SRS-A antagonists.
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Doi:10.1016/S0040-4039(01)80628-6
(1989)Doi:10.1016/S0022-328X(00)85700-9
(1982)Doi:10.1039/c4nj01893a
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(1982)