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Dicyclomine

Catalog No. DB00804 Name DrugBank
CAS Number 77-19-0 Website http://www.ualberta.ca/
M. F. C19H35NO2 Telephone (780) 492-3111
M. W. 309.4867 Fax (780) 492-1071
Purity Email david.wishart@ualberta.ca
Storage Chembase ID: 683

SYNONYMS

IUPAC name
2-(diethylamino)ethyl 1-cyclohexylcyclohexane-1-carboxylate
IUPAC Traditional name
dicyclomine
Brand Name
Dicycloverine
Kolantyl Hydrochloride
Dicyclomine Hcl
Mamiesan
Dicyclomine Hydrochloride
Diethylaminocarbethoxybicyclohexyl Hydrochloride
Bentyl
Bentylol
Bentylol Hydrochloride
Di-Syntramine
Dicycloverin
Dyspas
Oxityl-P
Procyclomin
Wyovin
Atumin
Bentomine
Bentyl Hydrochloride
Dicicloverina [INN-Spanish]
Dicycloverin Hydrochloride
Dicycloverine Hydrochloride
Dicycloverinum [INN-Latin]
Diocyl
Diocyl Hydrochloride
Formulex
Merbentyl
Sawamin
Spasmoban
Wyovin Hydrochloride

DATABASE IDS

PubChem SID 46505371
CAS Number 77-19-0
PubChem CID 3042

PROPERTIES

Hydrophobicity(logP) 5.5

DETAILS

Description (English)
Item Information
Drug Groups approved
Description A muscarinic antagonist used as an antispasmodic and in urinary incontinence. It has little effect on glandular secretion or the cardiovascular system. It does have some local anesthetic properties and is used in gastrointestinal, biliary, and urinary tract spasms. [PubChem]
Indication For the treatment of functional bowel/irritable bowel syndrome
including Colicky abdominal pain; diverticulitis
Pharmacology Dicyclomine is an anticholinergic drug, a medication that reduces the effect of acetylcholine, a chemical released from nerves that stimulates muscles, by blocking the receptors for acetylcholine on smooth muscle (a type of muscle). It also has a direct relaxing effect on smooth muscle. Dicyclomine is used to treat or prevent spasm in the muscles of the gastrointestinal tract in the irritable bowel syndrome. In addition, Dicyclomine inhibits gastrointestinal propulsive motility and decreases gastric acid secretion and controls excessive pharyngeal, tracheal and bronchial secretions.
Affected Organisms
Humans and other mammals
Protein Binding >99%
Elimination The principal route of elimination is via the urine (79.5% of the dose). Excretion also occurs in the feces, but to a lesser extent (8.4%).
Distribution * 3.65 L/kg [20 mg oral dose]
External Links
Wikipedia
RxList
Drugs.com

REFERENCES