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Research using MC4R knockout mice and selective MC4R antagonists has established MC4R as the primary receptor mediating MT-IIs pro-erectile and pro-sexual effects with MC4R-null mice showing substantially reduced or absent MT-II-induced erections and sexual behaviour, and MC4R-selective antagonists blocking these responses at doses not affecting MT-IIs melanogenic activity

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In contrast, more severe toxicity was observed when rat or human liver slices were incubated with AMAP than when mouse liver slices were incubated with the compound, or when rat and human liver slices were incubated with acetaminophen