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Amantadine Hydrochloride

Amantadine Hydrochloride

Product ID A4802
Cas No. 665-66-7
Purity ≥98%
Product Unit SizeCostQuantityStock
5 g $75.10 In stock
25 g $142.80 In stock
100 g $300.40 In stock
Bulk Quote

Quicklinks

  • Description
  • Product Info
  • Shipping and Storage
  • Downloads
  • References
  • Description
  • Product Info
  • Shipping and Storage
  • Downloads
  • References
  • Custom Order

Description

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).

Product Info

Cas No.

665-66-7

Purity

≥98%

Formula

C10H17N • HCl

Formula Wt.

187.71

Chemical Name

Tricyclo[3.3.1.13,7]decan-1-amine hydrochloride

IUPAC Name

adamantan-1-amine;hydrochloride

Synonym

Amazolon, Mantadan, Mantadine, Symmetrel, Vitrofral

Melting Point

> 360°C (dec.)

Solubility

Soluble in water (400 mg/mL) or alcohol (196 mg/mL). Practically insoluble in ether.

Appearance

A white or almost white crystalline powder

Shipping and Storage

Store Temp

Ambient

Ship Temp

Ambient

Downloads

MSDS

A4802 MSDS PDF

Info Sheet

A4802 Info Sheet PDF

References

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.

Custom Order

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