THE PHARMACOLOGY OF ISAMOXOLE [2‐METHYL‐N‐BUTYL‐N(4‐METHYLOXAZOL‐2‐YL) PROPANAMIDE] LRCL 3950, A NEW ANTI‐ALLERGIC COMPOUND
Open Access
- 1 February 1980
- journal article
- Published by Wiley in British Journal of Pharmacology
- Vol. 71 (2) , 387-398
- https://doi.org/10.1111/j.1476-5381.1980.tb10951.x
Abstract
1 Isamoxole [2-methyl-N-butyl-N(4-methyloxazol-2-yl) propanamide] is an effective orally active anti-allergic compound in animals. 2 Isamoxole inhibits the immunological release of mediators, notably slow-reacting substance of anaphylaxis (SRS-A) from sensitized human and guinea-pig chopped lung in vitro. 3 In vivo, allergic responses were inhibited in guinea-pigs and rats by doses as low as 25 mg/kg given orally 180 and 30 min before challenge. The effect of Isamoxole was still present 4 h after a single dose of 100 mg/kg orally in the guinea-pig and 3 h in the rat. 4 Isamoxole is a moderately potent, selective inhibitor of SRS-A activity on the guinea-pig ileum in vitro, at concentrations that do not antagonize histamine, 5-hydroxytryptamine, or bradykinin. 5 Isamoxole causes human bronchial muscle to relax and antagonizes the bronchoconstriction induced by SRS-A.Keywords
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