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Amantadine exhibits neuroprotective and antiviral activity. Amantadine directly inhibits the viral M2 proton channel. This compound is also used to treat Parkinson’s disease; it inhibits monoamine oxidase A (MAO-A), α7 nicotinic acetylcholine receptors (nAChRs), norepinephrine transporters (NET), and NMDA receptors (through acceleration of channel closure).
| Cas No. | 31377-23-8 |
|---|---|
| Purity | ≥98% |
| Formula | (C10H17N)2 • H2SO4 |
| Formula Wt. | 400.58 |
| Chemical Name | Tricyclo[3.3.1.13,7]decan-1-amine sulfate |
| IUPAC Name | adamantan-1-amine;sulfuric acid |
| Synonym | PK-Merz, Trivaline |
| Melting Point | 300°C |
| Appearance | White to off white powder |
| Store Temp | Ambient |
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| Ship Temp | Ambient |
| MSDS | |
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| Info Sheet |
Sommerauer C, Rebernik P, Reither H, et al. The noradrenaline transporter as site of action for the anti-Parkinson drug amantadine. Neuropharmacology. 2012 Mar;62(4):1708-16. PMID: 22155208.
Jing X, Ma C, Ohigashi Y, et al. Functional studies indicate amantadine binds to the pore of the influenza A virus M2 proton-selective ion channel. Proc Natl Acad Sci U S A. 2008 Aug 5;105(31):10967-72. PMID: 18669647.
Blanpied TA, Clarke RJ, Johnson JW. Amantadine inhibits NMDA receptors by accelerating channel closure during channel block. J Neurosci. 2005 Mar 30;25(13):3312-22. PMID: 15800186.
Pearce J. Mechanism of action of amantadine. Br Med J. 1971 Aug 26;3(5773):529. PMID: 4327681.