My watch list  


Systematic (IUPAC) name
(4aS,6R,8aS)-5,6,9,10,11,12- hexahydro-3-methoxy-11-methyl-4aH-[1]benzofuro[3a,3,2-ef] [2]benzazepin-6-ol
CAS number 357-70-0
ATC code N06DA04
PubChem 9651
DrugBank APRD00206
Chemical data
Formula C17H21NO3 
Mol. mass 287.354 g/mol
Pharmacokinetic data
Bioavailability 80 to 100%
Protein binding 18%
Metabolism Hepatic partially CYP450:CYP2D6/3A4 substrate
Half life 7 hours
Excretion Renal (95%, of which 32% unchanged), fecal (5%)
Therapeutic considerations
Pregnancy cat.


Legal status

Rx and OTC

Routes Oral

Galantamine (trade names Razadyne, Razadyne ER, Reminyl, Nivalin) is a drug developed by Janssen Pharmaceutica, and used for the treatment of mild to moderate Alzheimer’s disease. It is an alkaloid that is obtained synthetically and from the bulbs and flowers of the Caucasian snowdrop (Voronov’snowdrop), Lycoris radiata (Red Spider Lily), Galanthus woronowii (Amaryllidaceae) and related species. The active ingredient was discovered accidentally by a Bulgarian pharmacologist in the 1950s.[1]



Galantamine in its pure form is a white powder. Galantamine is a competitive and reversible cholinesterase inhibitor. It is believed it works by enhancing cholinergic function by increasing the concentration of acetylcholine in the brain. The atomics resolution 3D structure of the complex of galantamine and its target, acetylcholinesterase, was recentely determined by X-ray crystallography.[2] There is no evidence that galantamine alters the course of the underlying dementing process.[3] Galantamine has also shown activity in modulating the nicotinic cholinergic receptors to increase acetylcholine release.[4]


Absorption of galantamine is rapid and complete and shows linear pharmacokinetics. It is well absorbed with absolute oral bioavailability between 80 and 100%. It has a half-life of 7 hours. Peak effect of inhibiting acetylcholinesterase was achieved about one hour after a single oral dose of 8 mg in healthy volunteers.

Plasma protein binding of galantamine is about 18%, which is relatively low.


The major route of metabolism for galantamine is through the liver, this accounts for approximately 75% of the total metabolism of galantamine. Hepatic cytochrome P450 (CYP) isoenzymes are the active enzymes for this metabolic route. In vitro studies have shown that CYP2D6 and CYP3A4 are involved in galantamine metabolism.

For Razadyne ER (the once-a-day formulation), CYP2D6 poor metabolizers had drug exposures that were approximately 50% higher than for extensive metabolizers. About 7% of the population has this genetic mutation, however because the drug is individually titrated to tolerability, no specific dosage adjustment is necessary for this population.

Clinical use


Galantamine is indicated for mild to moderate dementia of the Alzheimer’s type.

The U.S. Food and Drug Administration (FDA) sent out a warning indicating that the product should not be used in patients of mild cognitive impairment (MCI) because of increased mortality observed in trials for MCI with galantamine.[5]

Available forms

The product is supplied in twice-a-day tablets, once-a-day extended release capsules, and in oral solution. The tablets come in 4mg, 8mg and 12mg forms. The capsules come in 8mg, 16mg, and 24mg forms.

Adverse events

In clinical trials, galantamine’s side effect profile was very similar to that of other cholinesterase inhibitors, with gastrointestinal symptoms being the most notable and most commonly observed. In practice, some other cholinesterase inhibitors might be better tolerated; however, a careful and gradual titration over more than three months may lead to equivalent long-term tolerability.[6]

Other use

Supplement for lucid dream and out-of-body experience

Some people who practice lucid dream (LD) or out-of-body experience (OBE) use Galantamine to increase their odds to achieve LD or OBE. [7] [8] [9] By taking small amount of Galantamine (around 4 to 8 mg) after 5 to 6 hours of deep sleep and practice the induction technique such as meditation, MILD or WILD [2] many people report more success with Galantamine. [10]

There are also reports that taking Galantamine without proper induction technique will not lead to LD or OBE but will result in only a vivid dream instead.

Galantamine used with Choline bitartrate or Alpha-GPC is said to increase your odds of becoming Lucid.

Some people report mixing Galantamine with other nootropic can enhance the degree of lucidity, but this is still controversial since some mixtures may work for some people, but lead to failure for others.


Along with other cholinergics or acetylcholinesterase inhibitors such as Huperzine A, Galantamine also has been used as nootropic or "brain enhancer".

Total synthesis

Galantamine is produced from natural resources and a patented total synthesis process. Many other synthetic methods exist but have not been implemented on an industrial scale.


  1. ^ Scott LJ, Goa KL. Adis Review: Galantamine: a review of its use in Alzheimer's disease. Drugs 2000;60(5):1095-122 PMID 11129124
  2. ^ Greenblatt, HM, Kryger, G, Lewis, T, Silman, I, Sussman, JL "Structure of acetylcholinesterase complexed with (-)-galanthamine at 2.3Å resolution" FEBS Lett 1991; 463, 321-26. PMID 10606746
  3. ^ Ortho-McNeil Neurologics, “Razadyne ER US Product Insert”, May 2006. [1]
  4. ^ Woodruff-Pak DS, Vogel RW 3rd, Wenk GL, “Galantamine: effect on nicotinic receptor binding, acetylcholinesterase inhibition, and learning” Proc Natl Acad Sci U S A. 2001 Feb 13;98(4):2089-94. PMID 11172080
  5. ^ Alert for Healthcare Professionals on Galantamine
  6. ^ Birks J. “Cholinesterase inhibitors for Alzheimer's disease.” Cochrane Database Syst Rev. 2006 Jan 25;(1):CD005593. PMID 16437532
  7. ^ Thomas Yuschak (2006). Advanced Lucid Dreaming, 1st ed., Lulu Enterprises. ISBN 978-1-4303-0542-2. 
  8. ^ Thomas Yuschak (2007). Pharmacological Induction of Lucid dreams. 
  9. ^ Substances that enhance recall and lucidity during dreaming. Stephen LaBerge - US Patent. Retrieved on 2007-10-29.
  10. ^ Galantamine LDS Profile. Yuschak LDS Profiles. Retrieved on 2007-10-29.
This article is licensed under the GNU Free Documentation License. It uses material from the Wikipedia article "Galantamine". A list of authors is available in Wikipedia.
Your browser is not current. Microsoft Internet Explorer 6.0 does not support some functions on Chemie.DE