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Clandilon: Full Drug Profile
Medically reviewed by Min Clinic Staff | Updated: January 2026
Clandilon - General Information
A direct-acting smooth muscle relaxant used to dilate blood vessels. It may cause gastrointestinal distress and tachycardia. Clandilon is not approved for use in the U.S. or Canada, but is approved in various European countries.
Pharmacology of Clandilon
Clandilon is in a class of drugs called vasodilators. Clandilon relaxes veins and arteries, which makes them wider and allows blood to pass through them more easily.
Additional information about Clandilon
- Clandilon Indication
Used in the treatment of various blood vessel diseases (e.g., claudication, arteriosclerosis and Raynaud's disease) and nighttime leg cramps.
- Mechanism Of Action
- Clandilon produces peripheral vasodilation by a direct effect on vascular smooth muscle.
- Food Interactions
- Take with food to reduce irritation.
- Generic Name
- Cyclandelate
- Synonyms
- Cyclandelic acid; Ciclandelato [inn-spanish]; Cyclandelatum [inn-latin]; 3,5,5-Trimethylcyclohexyl mandelate; 3,5,5-Trimethylcyclohexyl amygdalate; 3,3,5-Trimethylcyclohexyl mandelate
- Drug Category
- Vasodilator Agents
- Drug Type
- Small Molecule; Approved
- Other Brand Names containing Cyclandelate
- Arto-espasmol; Capilan; Ciclospasmol; Clandilon; Cyclergine; Cyclobral; Cyclolyt; Cyclomandol; Cyclospasmol; Dilatan; Natil; Novodil; Perebral; Saiclate; Sancyclan; Sepyron; Spasmione; Spasmocyclon; Spasmocyclone; Vasodyl;
- Absorption
- Well absorbed following oral administration.
- Toxicity (Overdose)
- Acute oral toxicity (LD50): 3950 mg/kg [Guinea pig]
- Dosage Forms of Clandilon
- Tablet Oral
- Chemical IUPAC Name
- (3,3,5-trimethylcyclohexyl) 2-hydroxy-2-phenylacetate
- Chemical Formula
- C17H24O3
- Organisms Affected
- Humans and other mammals
