Abstract
Lisuride hydrogen maleate [1,1 diethyl-3-(9,10-didehydro-6-methyl-8α-ergolinyl] urea is the first derivative of isolysergic acid in clinical use. It is an 8-α-aminoergoline and was synthesized by Zikan and Semonsky (1968). It is a white slightly bitter tasting substance, which is reasonably stable at room temperature if not exposed to light. Lisuride hydrogen maleate is soluble in water or saline up to 1 mg/ml. Owing to its low effective dose, it is therefore the first dopamine agonist which can also be used on a parenteral basis (Dorow et al. 1980).
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References
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Gopinathan, G., Horowski, R., Suchy, I.H. (1989). Lisuride Pharmacology and Treatment of Parkinson’s Disease. In: Calne, D.B. (eds) Drugs for the Treatment of Parkinson’s Disease. Handbook of Experimental Pharmacology, vol 88. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-73899-9_19
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