Isocyclamine

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An anticholinergic drug


Isocyclamine
INN
Drug class
Routes of administration
Pregnancy category
Bioavailability
Metabolism
Elimination half-life
Excretion
Legal status
CAS Number 77-29-8
PubChem 7180
DrugBank
ChemSpider 6910
KEGG D04695


Isocyclamine is a pharmaceutical drug that belongs to the class of anticholinergic agents. It is primarily used for its effects on the nervous system, particularly in the treatment of gastrointestinal disorders and spasms.

Chemical Structure and Properties[edit | edit source]

Chemical structure of isocyclamine

Isocyclamine is chemically known as 2-(1-cyclohexyl-1-phenyl-3-pyrrolidinyl)ethanol. It has a molecular formula of C18H27NO and a molecular weight of 273.42 g/mol. The structure consists of a pyrrolidine ring, a cyclohexane ring, and a phenyl group, which contribute to its anticholinergic properties.

Pharmacology[edit | edit source]

Isocyclamine acts as an anticholinergic agent by inhibiting the action of the neurotransmitter acetylcholine at muscarinic receptors. This inhibition leads to a decrease in involuntary muscle movements and secretions, making it useful in treating conditions like irritable bowel syndrome and other gastrointestinal disorders characterized by excessive motility and spasms.

Medical Uses[edit | edit source]

Isocyclamine is used in the management of various conditions that benefit from its anticholinergic effects. These include:

Side Effects[edit | edit source]

The use of isocyclamine can lead to several side effects, typical of anticholinergic drugs. These may include:

Mechanism of Action[edit | edit source]

Isocyclamine works by blocking the muscarinic acetylcholine receptors in the central nervous system and peripheral nervous system. This blockade reduces the effects of acetylcholine, leading to decreased muscle contractions and secretions in the gastrointestinal tract.

Synthesis[edit | edit source]

The synthesis of isocyclamine involves the reaction of cyclohexanone with phenylmagnesium bromide to form a tertiary alcohol, which is then reacted with pyrrolidine to yield the final product.

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Contributors: Prab R. Tumpati, MD