| Identification | More | [Name]
Rivastigmine | [CAS]
123441-03-2 | [Synonyms]
EXELON
RIVASTIGMINE
RIVASTIGMINE HYDROGEN TARTRATE
RIVASTIGMINE TARTRATE
(s)-n-ethyl-3-[(1-dimethylamino)ethyl]-n-methylphenylcarbamate hydrogen tartrate
RIVASTIGIMINE(FORR&DONLY)
3-((1S)-1-(Dimethylamino)ethyl)phenyl N-ethyl-N-methylcarbamate
Ethylmethylcarbamic acid 3-((1S)-1-(dimethylamino)ethyl)phenyl ester | [EINECS(EC#)]
602-936-0 | [Molecular Formula]
C14H22N2O2 | [MDL Number]
MFCD03700731 | [Molecular Weight]
250.34 | [MOL File]
123441-03-2.mol |
| Hazard Information | Back Directory | [Uses]
Antidepressant | [Definition]
ChEBI: A carbamate ester obtained by formal condensation of the carboxy group of ethyl(methyl)carbamic acid with the phenolic OH group of 3-[(1S)-1-(dimethylamino)ethyl]phenol. A reversible cholinesterase inhibitor. | [Brand name]
Exelon (Novartis). | [General Description]
Rivastigmine (Exelon, EA 713) is apseudoirreversible noncompetitive carbamate inhibitor ofAChE. Although the half-life is approximately 2 hours,the inhibitory properties of this agent last for 10 hours becauseof the slow dissociation of the drug from the enzyme.The Food and Drug Administration (FDA) approved its usein mild-to-moderate Alzheimer disease in April 2000. InJuly 2007, rivastigmine was granted approval for use inmanaging mild-to-moderate dementia associated withParkinson disease. | [Pharmacokinetics]
Rivastigmine is a centrally selective, arylcarbamate AChEI that was approved in 2000 for oral administration in the treatment of AD. It has an
elimination half-life of 1.4 to 1.7 hours but is able to inhibit AChE for up to 10 hours. Because of the slow dissociation of the carbamylated
enzyme, it has been referred to as a pseudo-irreversible AChEI. Like donepezil, rivastigmine exhibits a low level of hepatotoxicity. It is
rapidly and extensively hydrolyzed in the CNS by cholinesterase with minimal involvement of CYP450. The phenolic metabolite is excreted
primarily via the kidneys. | [Clinical Use]
Mild-moderate dementia in Alzheimer’s disease
Idiopathic Parkinson’s disease | [Drug interactions]
Potentially hazardous interactions with other drugs
Muscle relaxants: enhances effect of suxamethonium;
antagonises effect of non-depolarising muscle
relaxants. | [Metabolism]
Rivastigmine is the tertiary amines that
are rapidly absorbed from the gastrointestinal tract, as
are tacrine, donepezil, and galanthamine, whereas quaternary
ammonium compounds are poorly absorbed
after oral administration. Nevertheless, quaternary ammonium
compounds like neostigmine and pyridostigmine
are orally active if larger doses are employed.
Only the quaternary ammonium inhibitors do not readily
enter the CNS. Because of their high lipid solubility
and low molecular weight, most of the organophosphates
are absorbed by all routes of administration;
even percutaneous exposure can result in the absorption
of sufficient drug to permit the accumulation of
toxic levels of these compounds. |
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