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Chemical Methysergide

Name Methysergide
CAS Type 1 Name Ergoline-8-carboxamide, 9,10-didehydro-N-(1-(hydroxymethyl)propyl)-1,6-dimethyl-, (8beta(S))-
Equivalent Terms Deseril | D├ęsernil Sandoz | D├ęsernil-Sandoz | Desril | Dimaleate, Methysergide | Dimethylergometrin | Maleate, Methysergide | Methylmethylergonovine | Methysergide Dimaleate | Methysergide Maleate | Sansert | UML491 | UML 491 | UML-491
CAS Registry Number 361-37-5
Definition An ergot derivative that is a congener of LYSERGIC ACID DIETHYLAMIDE. It antagonizes the effects of serotonin in blood vessels and gastrointestinal smooth muscle, but has few of the properties of other ergot alkaloids. Methysergide is used prophylactically in migraine and other vascular headaches and to antagonize serotonin in the carcinoid syndrome.
Structure Methysergide
Top Interacting
Genes
MeSH® ID D008784
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Top ↑ Ancestors

1. ChemicalsHeterocyclic Compounds Has associated genes Has associated diseases Has associated phenotype references Has associated exposure references Alkaloids Has associated genes Has associated diseases Has associated phenotype references Has associated exposure references Ergot Alkaloids Has associated genes Has associated diseases Has associated phenotype references Ergolines Has associated genes Has associated diseases Has associated phenotype references Methysergide Has associated genes Has associated diseases Has associated phenotype references
2. ChemicalsHeterocyclic Compounds Has associated genes Has associated diseases Has associated phenotype references Has associated exposure references Heterocyclic Compounds, Fused-Ring Has associated genes Has associated diseases Has associated phenotype references Has associated exposure references Heterocyclic Compounds, 4 or More Rings Has associated genes Has associated diseases Has associated phenotype references Has associated exposure references Ergolines Has associated genes Has associated diseases Has associated phenotype references Methysergide Has associated genes Has associated diseases Has associated phenotype references

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None.