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Scopolamine, also known as levo-duboisine, and hyoscine, is a tropane alkaloid drug (Medication) with muscarinic antagonist effects. It is obtained from plants of the family Solanaceae (nightshades), such as henbane, jimson weed and Angels Trumpets (Datura resp. Brugmansia spec.), and corkwood (Duboisia species ). It is among the secondary metabolites of these plants. Therefore, scopolamine is one of three main active components of belladonna and stramonium tinctures and powders used medicinally along with atropine and hyoscyamine. Scopolamine was isolated from plant sources by scientists in 1881 in Germany and description of its structure and activity followed shortly thereafter.

Scopolamine has anticholinergic properties and has legitimate medical applications in very minute doses. As an example, in the treatment of motion sickness, the dose, gradually released from a transdermal patch, is only 330 microgrammes (�g) per day. In rare cases, unusual reactions to ordinary doses of scopolamine have occurred including confusion, agitation, rambling speech, hallucinations, paranoid behaviors, and delusions.

Watchedfields: changed

Verifiedrevid: 306795873

Iupac Name: (-)-(''S'')-3-hydroxy-2-phenyl-propionic acid (1''R'',2''R'',4''S'',7''S'',9''S'')-9-methyl-3-oxa-9-aza-tricyclo3.3.1.02,4non-7-yl ester

Image2: Scopolamine_structure.png

Casno Ref: cascite

Number on List: 51-34-3

Chemspiderid: 10194106

Atc Prefix: A04

Atc Suffix: AD01

Atc Supplemental: ATCN05CM05, ATCS01FA02

Pubchem: 5184

Drugbank: DB00747

C: 17 H=21 N=1 O=4

Molecular Weight: 303.353 g/mol

Bioavailability: 10 - 50%

Elimination Half-life: 4.5 hours

Pregnancy Us: C

Legal Us: Rx-only

Legal Uk: P

Routes Of Administration: transdermal, ocular, oral, subcutaneous, intravenous, sublingual, rectal, buccal transmucousal, intramuscular

source: wikipedia.org

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