This is a preview of subscription content, access via your institution
Access options
Subscribe to this journal
Receive 12 print issues and online access
$209.00 per year
only $17.42 per issue
Buy this article
- Purchase on Springer Link
- Instant access to full article PDF
Prices may be subject to local taxes which are calculated during checkout
References
Mayeux, R. & Sano, M. Treatment of Alzheimer's disease. N. Engl. J. Med. 341, 1670–1679 (1999).
Kemp, J. A. & McKernan, R. M. NMDA receptors as drug targets. Nature Neurosci. 5, 1039–1042 (2002).
Parsons, C. G., Danysz, W. & Quack, G. Memantine is a clinically well-tolerated N-methyl-D-aspartate (NMDA) receptor antagonist — a review of the preclinical data. Neuropharmacology 38, 735–767 (1999).
Gerzon, K. et al. The adamantyl group in medicinal agents. I. Hypoglycemic N-arylsulfonyl-N′-adamantylureas. J. Med. Chem. 6, 760–763 (1963).
Bormann, J. Memantine is a potent blocker of N-methyl-D-aspartate (NMDA) receptor channels. Eur. J. Pharmacol. 166, 591–592 (1989).
Reisberg, B. et al. Memantine in moderate-to-severe Alzheimer's disease. N. Engl. J. Med. 348, 1333–1345 (2003).
FDA Drug Approvals List [online] (cited 10 April 2004) <http://www.fda.gov/cder/foi/label/2003/021487lbl.pdf> (2003).
Alzheimer's Disease (Decision Resources, Waltham, Massachusetts, Pharmacor, 2004).
Tavorath, R. & Hesketh, P. J. Drug treatment of chemotherapy-induced delayed emesis. Drugs 52, 639–648 (1996).
Navari, R. M. et al. Reduction of cisplatin-induced emesis by a selective neurokinin-1 receptor antagonist. N. Engl. J. Med. 340, 190–195 (1999).
Rupniak, N. M. J. & Kramer, M. S. Discovery of the antidepressant and anti-emetic efficacy of substance P receptor (NK1) antagonists. Trends Pharmacol. Sci. 20, 485–490 (1999).
Hale, J. J. et al. Structural optimization affording 2-(R)-(1-(R)-3,5 bis(trifluoromethyl)phenylethoxy)-3-(S)-(4-fluoro)phenyl-4-(3-oxo-1,2,4-triazol-5-yl) methylmorpholine, a potent, orally active, long-acting morpholine acetal human NK-1 receptor antagonist. J. Med. Chem. 41, 4607–4614 (1998).
Hesketh, P. J. et al. The oral neurokinin-1 antagonist aprepitant for the prevention of chemotherapy-induced nausea and vomiting: a multinational, randomized, double-blind, placebo-controlled trial in patients receiving high-dose cisplatin — the Aprepitant Protocol 052 Study Group. J. Clin. Oncol. 21, 4112–4119 (2003).
Emend prescribing information [online] (cited 12 April 2004) <http://www.emend.com/emend/shared/documents/pi.pdf> (2003).
Clark, R. D. et al. 2-(quinuclidin-3-yl)pyrido[4,3-b]indol-1-ones and isoquinolin-1-ones. Potent conformationally restricted 5-HT3 receptor antagonists. J. Med. Chem. 36, 2645–2657 (1993).
Eglen, R. M. et al. Pharmacological characterization of RS 25259-197, a novel and selective 5-HT3 receptor antagonist, in vivo. Br. J. Pharmacol. 114, 860–866 (1995).
Aloxi prescribing information [online] (cited 12 April 2004) <http://www.aloxi.com/images/downloads/pi.pdf> (2003).
Gralla, R. et al. Palonosetron improves prevention of chemotherapy-induced nausea and vomiting following moderately emetogenic chemotherapy: results of a double-blind randomized phase III trial comparing single doses of palonosetron with ondansetron. Ann. Oncol. 14, 1570–1577 (2003).
Additional information
Authorship This section was authored by Andrea Witt, Nancy Macdonald and Peter Kirkpatrick, and includes material first published in Nature Reviews Drug Discovery. Andrea Witt and Nancy Macdonald are at Decision Resources Inc., 260 Charles Street, Waltham, Massachusetts 02453, USA. Peter Kirkpatrick is at Nature Reviews Drug Discovery.
Rights and permissions
About this article
Cite this article
Neurological disorders. Nat Rev Drug Discov 3 (Suppl 7), S38–S40 (2004). https://doi.org/10.1038/nrd1411
Issue Date:
DOI: https://doi.org/10.1038/nrd1411