Galantamine chemical structure Scheme 1. Trost 2005 Galanthamine total synthesis:a bromine, sodium acetate, acetic acid, iron, rt b potassium carbonate, 2days c  Troc-Cl, DMAP, Pyridine, dichloromethane d palladium,Trost ligand, triethylamine, dichloromethane e 1.5 mol % TsOH, CH(OMe)3, methanol f DIBAL-H, toluene, -78 °C, 1 hr g  triphenylphosphine, acetonecyanohydrin, DIAD, diethyl ether h 2.20 mol % TsOH, THF, water i  15 mol % Palladium(II) acetate, 15 mol% dppp, 3 eq. Ag2CO3, toluene, 107 °C j selenium dioxide  disodium hydrogen phosphate dioxane, 150 °C 3 hrs k  methylamine ,methanol l 4 eq. DIBAL-H, m aqueous NaH2PO4 n NaCNBH3
Find information on thousands of medical conditions and prescription drugs.

Galantamine

Galantamine (trade name Razadyne®, Reminyl®) is a medication used in the treatment of Alzheimer's disease. more...

Home
Diseases
Medicines
A
B
C
D
E
F
G
Gabapentin
Gabitril
Galantamine
Gamma-hydroxybutyrate
Ganciclovir
Garamycin
Gaviscon
Gemcitabine
Gemfibrozil
Gemhexal
Gemzar
Generlac
Gentamicin
Geodon
Gleevec
Gliadel
Gliadel Wafer
Glibenclamide
Glimepiride
Glipizide
Glucagon
Glucobay
Glucohexal
Glucophage
Glucosamine
Glucotrol
Glutethimide
Golytely
Gonadorelin
Goserelin
Gramicidin
Gramicidin S
Granisetron
Grifulvin V
Griseofulvin
Guaifenesin
H
I
J
K
L
M
N
O
P
Q
R
S
T
U
V
W
X
Y
Z

Galantamine is mostly used as hydrobromide salt. It is a centrally acting reversible cholinesterase inhibitor in the same class as donepezil. Galantamine has a much shorter half life than donepezil (there is a newer prolonged release version available in 2004) and it also has more nicotinic receptor activity and is potentially more stimulating but also probably because of this activity tends to cause worse gastrointestinal side effects.

Total synthesis

The natural source of galantamine are certain species of daffodil and because these species are scarce and because the isolation of galanthamine from daffodil is expensive (a 1996 figure specifies 50,000 US dollar per kilogram) alternative synthetic sources are under development by means of total synthesis. One recent publication details the enantioselective organic synthesis of galanthamine and also that of morphine from a single precursor .

The total synthesis of galanthamine (Trost 2005) is described as follows (see scheme 1): the sequence starts by bromination by electrophilic aromatic substitution of isovanillin 1 to bromophenol 2, then by synthesis of the second intermediate 5 by reacting dialdehyde 3 in a coupled aldol reaction and Horner-Wadsworth-Emmons reaction with trimethyl phosphonoacetate 4. The hydroxyl group is activated as a leaving group by acetylation with trichloroethyl carbonate (Troc) to 6. Next an enantioselective Trost AAA reaction takes place between bromophenol 2 and carbonate 6 to the allyl ether 7. Next the aldehyde group is protected as an acetal in 8 and this step enables the to organic reduction of the ester group to the alcohol 9 with DIBAH and subsequent conversion of this alcohol to a nitrile by nucleophilic displacement to 10 followed by aldehyde deprotection to 11. The intramolecular Heck reaction to 12 creates the dihydrofuran ring. Allylic oxidation by selenium dioxide provides allylic alcohol 13 with the correct stereochemistry. The aldehyde reacts with methylamine to the imine 14 and reduction of the imine and nitrile by DIBAL-H leading to ring-closure to the hemi-aminal 15 (not isolated) followed by acid quenching gives the alcohol 16. In the final step this alcohol group is reduced to give Galanthamine 17 together with 6% of the epi isomer 18.

Read more at Wikipedia.org


[List your site here Free!]


Drug therapy for patients with Alzheimer's disease
From American Family Physician, 5/15/05 by Bill Zepf

The number of persons in the United States who were diagnosed with Alzheimer's disease in the year 2000 was 4.5 million. The prevalence of Alzheimer's disease increases with age, affecting 1 percent of patients 60 years of age, but rising to 30 percent of those 85 years of age. Cummings reviewed the management of this commonly encountered cause of dementia.

Alzheimer's disease is marked by a steady decline in cognitive function, accompanied by mood and behavior disturbances, especially as the disease progresses. Motor or sensory abnormalities, gait disturbances, and seizures typically do not occur, although these may appear in the later stages. Increasing evidence indicates that the accumulation of neurotoxic beta-amyloid peptide plays a central role in this debilitating disorder. The neurofibrillary tangles, inflammation, and oxidation effects that received attention early in the investigations of Alzheimer's disease appear to be secondary effects precipitated by deposition of this peptide.

The author notes that the initial work-up of a patient with suspected dementia should include screening measures for causes other than Alzheimer's disease. Thyroid function testing, vitamin 812 level, complete blood count, and a comprehensive metabolic panel (i.e., serum electrolytes, renal function, hepatic function) typically are included in the laboratory screen. The review author recommends a screening brain imaging study (computed tomography or magnetic resonance imaging) during the work-up as well.

Treatment of Alzheimer's disease has proved to be difficult. Options available to date have produced modest benefits in slowing the decline in cognitive function. Results of drug therapy trials typically have shown improvements of 2.5 to 3.5 points on a 70-point scale of cognitive function. This represents about a six-month reversal in the usual 7-point decrease in function that occurs annually in persons with Alzheimer's disease. Therapies specifically targeted to beta-amyloid peptide are under investigation, but none has been produced yet. Antioxidants, principally vitamin E, have not been shown to improve cognitive function in patients with Alzheimer's disease, but can delay progression to some clinical milestones (e.g., placement in a nursing home). Higher dosages of vitamin E supplementation (i.e., 2,000 IU daily) are advocated by some for patients with Alzheimer's disease. Although brain inflammation is evident in Alzheimer's disease, prospective trials of steroidal and nonsteroidal anti-inflammatory drugs have failed to show benefit. Hormone therapy in women with dementia initially was thought to be beneficial, but this was not borne out in prospective trials.

The mainstay of drug therapy for patients with Alzheimer's disease is cholinesterase inhibitors (see accompanying table) for patients with mild to moderate dysfunction. Tacrine is used rarely because of hepatoxicity. The other three agents (i.e., donepezil, galantamine, and rivastigmine) appear to be largely equivalent in efficacy. The nausea, vomiting, diarrhea, and other side effects that accompany these agents may be ameliorated by a slow titration of dosing and giving the medications with meals. The review author suggests waiting up to four weeks between dose escalations to decrease the adverse effects.

Memantine is a newer medication for the treatment of Alzheimer's disease that works by antagonizing the N-methyl-D-aspartate receptor. The U.S. Food and Drug Administration has approved memantine for treatment of moderate to severe Alzheimer's disease, and it may be used in combination with a cholinesterase inhibitor. The cognitive benefits seen with this agent have been modest as well. To date, no serious adverse effects from memantine are apparent.

Management of depression, agitation, and other neuropsychiatric symptoms often becomes necessary as Alzheimer's disease progresses, and the review article covers this area as well. Use of antidepressants and other psychotropic medications tends to follow usual guidelines, with the exception that tricyclic antidepressants usually are avoided, owing to their anticholinergic properties.

The author notes that caregivers of patients with Alzheimer's disease tend to report more physical and mental health problems than their peers. Referral of caregivers to community assistance organizations that deal with Alzheimer's disease may help decrease their burden.

Cummings JL. Alzheimer's disease. N Engl J Med July 1, 2004;351:56-67.

COPYRIGHT 2005 American Academy of Family Physicians
COPYRIGHT 2005 Gale Group

Return to Galantamine
Home Contact Resources Exchange Links ebay