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1-AdaMantanethylaMine

1-AdaMantanethylaMine Structure
CAS No.
13392-28-4
Chemical Name:
1-AdaMantanethylaMine
Synonyms
RIMANTADINE;LEVOFLOXACIN HCL;RiMantidine;1-Adamantanemethylamine;RiMantadine (FluMadine);1-Adaman;AKOS B022266;1-Rimantadine;AKOS NCG1-0034;1-Adamantanethylamine
CBNumber:
CB7122907
Molecular Formula:
C12H21N
Molecular Weight:
179.3
MOL File:
13392-28-4.mol
MSDS File:
SDS
Modify Date:
2024/7/2 8:55:15

1-AdaMantanethylaMine Properties

Boiling point 248°C
Density 1.033
Flash point 99°C
storage temp. Store at -20°C
solubility Soluble in DMSO
form Liquid
pka 11.17±0.29(Predicted)
color Colorless to light yellow
CAS DataBase Reference 13392-28-4(CAS DataBase Reference)
NIST Chemistry Reference 1-Adamantanemethylamine, «alpha»-methyl-(13392-28-4)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H302-H315-H319-H335
Precautionary statements  P261-P280-P301+P312-P302+P352-P305+P351+P338
HazardClass  IRRITANT
HS Code  2902190000

1-AdaMantanethylaMine Chemical Properties,Uses,Production

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).

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.

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.

1-AdaMantanethylaMine Preparation Products And Raw materials

Global( 246)Suppliers
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SynZeal Research Pvt Ltd +1 226-802-2078 Gujarat, India 6522 58 Inquiry
Hebei Mojin Biotechnology Co., Ltd +8613288715578 China 12450 58 Inquiry
Hangzhou FandaChem Co.,Ltd. 008657128800458; +8615858145714 China 9332 55 Inquiry
career henan chemical co +86-0371-86658258 +8613203830695 China 29894 58 Inquiry
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Chongqing Chemdad Co., Ltd +86-023-6139-8061 +86-86-13650506873 China 39916 58 Inquiry
CONIER CHEM AND PHARMA LIMITED +8618523575427 China 49391 58 Inquiry
Guangzhou Yuheng Pharmaceutical Technology Co., Ltd +8613580539051 CHINA 21149 58 Inquiry
SIMAGCHEM CORP +86-13806087780 China 17367 58 Inquiry
Hubei Ipure Biology Co., Ltd +8613367258412 China 10326 58 Inquiry

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1-AdaMantanethylaMine Spectrum

1-Adamantan-1-ylethylamine 1-Adamantanethylamine Rimantadine & Rimantadine Hydrochloride 1-(adaMantan-1-yl)ethanaMine hydrochloride 1-(AdaMantan-1-yl)ethanaMine 1-Adaman 1-ADAMANTANEMETHYLAMINE, alpha-METHYL-, HYDROCHLORIDE Adamantane, 1-(1-aminoethyl)-, hydrochloride Rimantadine hydrochloride [USAN] Tricyclo(3.3.1.13,7)decane-1-methanamine, alpha-methyl-, hydrochloride (9CI) α-Methyl-1-adamantanemethylamine 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- 1-(1-ADAMANTYL)ETHYLAMINE AKOS NCG1-0034 AKOS B022266 Levofloxacine Hydrochloride Flunarizine hydrochloride cp2000,BP98 Rimantadine (base and/or unspecified salts) α-Methyl-1-adamantanemethanamine (1R)-1-(1-adamantyl)ethanamine 1-Rimantadine Tricyclo[3.3.1.13,7]decane-1-methanamine, α-methyl- 1-AdaMantanethylaMine USP/EP/BP RiMantadine (FluMadine) RiMantidine RIMANTADINE LEVOFLOXACIN HCL 1-Adamantanemethylamine 13392-28-4 Antibiotics Antibiotics A to Z Antibiotics G-M BioChemical Adamantane derivatives API's Inhibitors