| Identification | More | [Name]
Rimantadine | [CAS]
13392-28-4 | [Synonyms]
1-(1-ADAMANTYL)ETHYLAMINE
AKOS B022266
AKOS NCG1-0034
LEVOFLOXACIN HCL
LEVOFLOXACIN HYDROCHLORIDE
RIMANTADINE
1-(1-Adamantyl)ethanamine
1-Adamantanemethylamine, alpha-methyl-
alpha-Methyl-1-adamantanemethylamine
alpha-Methyladamantanemethylamine
Tricyclo(3.3.1.13,7)decane-1-methanamine, alpha-methyl-
Tricyclo[3,3,1,1(3,7)]decane-1-methanamine, alpha-methyl-
Levofloxacine Hydrochloride
Flunarizine hydrochloride cp2000,BP98
Rimantadine (base and/or unspecified salts)
1-Adamantanemethylamine
α-Methyl-1-adamantanemethanamine | [EINECS(EC#)]
1308068-626-2 | [Molecular Formula]
C11H19N | [MDL Number]
MFCD03265511 | [Molecular Weight]
165.28 | [MOL File]
13392-28-4.mol |
| Questions And Answer | Back Directory | [Description]
Rimantadine (Brand name: Flumadine) is a kind of RNA synthesis inhibitor that used as an orally administrated antiviral drug in the prophylaxis and for the treatment of influenza. It is capable of shortening the duration and alleviated the symptoms of influenza. However, it is now not recommended for the treatment of influenza any longer due to the emergence of resistance problem since 2009. Its mechanism of action is not fully understood. It is indicated that it take effects through inhibiting the viral replication through possibly inhibiting the uncoating process of the virus. The virus M2 protein (an ion channel) seems to play an important role in the susceptibility of influenza A virus to the treatment of Rimantadine.
| [References]
https://www.drugbank.ca/drugs/DB00478
https://en.wikipedia.org/wiki/Rimantadine
|
| Hazard Information | Back Directory | [Uses]
Rimantadine act by blocking the M2 ion channel which is required for uptake of protons into the interior of the virus to permit acid-promoted viral uncoating (decapsidation).
| [Definition]
ChEBI: 1-(1-adamantyl)ethanamine is an alkylamine. | [Brand name]
Flumadine (Forest). | [General Description]
Resistant variants of influenza type A have been recoveredfrom rimantadine-treated patients.Resistance with inhibitory concentrations increased morethan 100-fold have been associated with single nucleotidechanges that lead to amino acid substitutions in the transmembranedomain of M2. rimantadineshare cross-susceptibility and resistance. | [Pharmaceutical Applications]
An analog of amantadine, supplied as the hydrochloride for
oral administration. | [Mechanism of action]
Rimantadine hydrochloride (α-methyl-1-adamantanemethylamine hydrochloride) is a synthetic adamatane
derivative that is structurally and pharmacologically related to amantadine. It appears to be more
effective than amantadine hydrochloride against influenza A, with fewer CNS side effects. Rimantadine
hydrochloride is thought to interfere with virus uncoating by inhibiting the release of specific proteins. It
may act by inhibiting RT or the synthesis of virus-specific RNA, but it does not inhibit virus adsorption or
penetration. It appears to produce a virustatic effect early in the virus replication. It is used widely in
Russia and Europe. | [Pharmacokinetics]
Oral absorption: >90%
Cmax 100 mg oral (every 12 h): 0.4–0.5 mg/L after 2–6 h
Plasma half-life: c. 35 h
Volume of distribution: Very large
Plasma protein binding: c. 40%
Absorption and distribution
Single- and multiple-dose pharmacokinetic studies in elderly patients and young adults are remarkably similar. The steadystate concentration in nasal mucus develops by day 5 at a concentration approximately 1.5-fold higher than plasma.
Metabolism
In contrast to amantadine, rimantadine is extensively metabolized in the liver by hydroxylation and glucuronidation.
Excretion
Less than 20% is excreted unchanged in the urine and most of the breakdown products are excreted by this route. Thus, the plasma half-life is much less affected by renal dysfunction than that of amantadine. | [Clinical Use]
Prophylaxis and treatment of influenza A H1N1 infections
Since prolonged administration is well tolerated by elderly
patients, the drug is preferable to amantadine. | [Clinical Use]
rimantadine is used for the treatment
of diseases caused by influenza A strains. | [Side effects]
Rimantadine has significantly fewer side effects than amantadine
at equivalent doses, perhaps because of differences
in pharmacokinetics, since with equal doses the blood levels
are considerably lower. CNS side effects are not significantly
higher than placebo. |
|
| Company Name: |
J & K SCIENTIFIC LTD.
|
| Telephone: |
18210857532 18210857532 |
| Website: |
https://www.jkchemical.com |
| Company Name: |
LETOPHARM LIMITED
|
| Telephone: |
+86-21-5821 5861 |
| Website: |
www.letopharm.com |
|