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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